2232 Clinical Research Jobs

This job is with Johnson & Johnson, an inclusive employer and a member of myGwork the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. At Johnson & Johnson,?we believe health is everything. Our strength in healthcare innovation empowers us to build a?world where complex diseases are prevented, treated, and cured,?where treatments are smarter and less invasive, and?solutions are personal.?Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.?Learn more at https://www.jnj.com Job Function Medical Affairs Group Job Sub Function Medical Science Liaison Job Category Scientific/Technology All Job Posting Locations: Bangalore, Karnataka, India, Chennai, Tamil Nadu, India Job Description Job Description: Johnson & Johnson is recruiting for Medical Science Liaison- Oncology, Medical Affairs located in Bangalore, India. The position reports to the TA Lead - Oncology, Johnson & Johnson Innovative Medicine, India. Position Overview Be a therapeutic area scientific expert where you will be scientific face of the company engaging in interactions with Key Opinion Leaders(KOL) discussing treatment trends, clinical trial data of our molecules and seeking insights that support the medical strategy. Key Responsibilities Primary scientific face of the organization to KOL&aposs for Oncology therapy area, responsible for: Identification, mapping and profiling of KOL&aposs of the given geography and therapy area on an ongoing basis Engagement of identified KOL&aposs through medical affairs initiatives in alignment with the overall franchise plan Represent the TA for medical & scientific affairs on all relevant cross functional teams and internal and external initiatives. Gathering customer insights and conveying them back to the franchise team Receiving and processing scientific information request received from Healthcare Professionals(HCP) Scientific resource for the sales team of the given therapy area responsible for regular training and flow of latest medical developments in the given field This is a highly collaborative role that requires excellent communication and influencing skills with all internal stakeholders to develop and implement medical strategy, to shape the external scientific landscape that can enable the fastest access to new products/indications for our patients, medical staff and the greater community. The position will require 70-80% travel for interaction with customers and various stakeholders. Qualifications - External Medical graduate (MD/ MBBS/ BDS /MDS) or Pharmaceutical university Degree ( PharmD or PhD) Experience And Skills Minimum of 0-2 years' experience in pharmaceutical/healthcare industry Good understanding of medical affairs function Understanding of local regulatory policy and industry&aposs code of practice related to drug registration, pharmaceutical promotion and clinical research. Are you ready to impact the world Johnson & Johnson offers an unusual experience to professionals looking for an opportunity to work with hardworking people who share your real passion for caring in an environment that empowers you to drive your own career. We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. Show more Show less

Dear Candidates, Immediate Vacancy for Pharma & Chemical Industries Qualification - Dip / Btech / Bsc / Msc / Micro / Mtech / Biotech / Chemistry / Chemical / Bio chemistry / Petro chemical / petroleum Fresher - Pharma Experience only can apply Designation - Quality Chemist / Quality Assurance / Production / Clinical Research / WTP / STP / ETP Location - Chennai / Hosur / Coimbatore Contact - Pooja HR - 7358119933 (Call Or Whatsapp) Share your Resume hr5jjjobs@gmail.com Venue Details: JJ Jobs S2, 1/44,2nd floor , parvathi Apartment / Bazar road jj nagar , Mogappair East Chennai -37 Land mark- MMM hospital website -jjjobs.co.in

As a Clinical Research (CRA) Manager at Medpace, you will play a crucial role in the clinical trial management process within our growing clinical operations team in Navi Mumbai, India. Your responsibilities will include line management of Clinical Research Associates (CRAs), overseeing recruitment, training, and development of CRAs, ensuring CRAs meet core monitoring responsibilities, managing CRA resourcing and allocation, as well as addressing turnover and retention to align with company objectives. To excel in this role, you should hold a Bachelor's degree with 4-6 years of experience in the pharmaceutical industry, specifically in clinical monitoring or study management. Ideally, you should have spent at least 3 years as a CRA and 1-2 years as a CRA Manager. Advanced knowledge of Good Clinical Practice is essential, along with strong leadership, mentoring, and communication skills. Proficiency in Microsoft Office software is required, and occasional travel for evaluating CRAs is expected (approximately 10% of the time). Medpace is a renowned full-service clinical contract research organization dedicated to accelerating the global development of safe and effective medical therapeutics. With expertise in various therapeutic areas such as oncology, cardiology, and central nervous system disorders, we operate in over 40 countries with a team of over 5,000 professionals. At Medpace, you will find a supportive work environment that values People, Purpose, and Passion. We offer competitive compensation and benefits packages, flexible work arrangements, structured career paths for professional growth, and employee appreciation events. Our commitment to employee health and wellness initiatives underscores our dedication to creating a positive workplace culture. Join us at Medpace and be part of a team that has been recognized by Forbes as one of America's Most Successful Midsize Companies multiple times. Our continuous receipt of CRO Leadership Awards speaks to our expertise, quality, reliability, and compatibility in the industry. If you are looking to make a real difference in the field of healthcare and contribute to improving the lives of patients worldwide, submit your qualifications for review. A member of the Medpace team will reach out if there is interest in moving forward with the next steps.,

Medpace, a rapidly growing global Clinical Research Organization (CRO), is excited to announce that we are looking for experienced professionals to join us as we prepare to launch our newest office in Hyderabad, India. This is more than just a job. It's an opportunity to be part of something from the very beginning. You will play a direct role in shaping the culture, building the team, and influencing how we grow in India. Your work will make a meaningful impact across global projects right from day one. Be a Founding Member: You will help establish and lead operations at our newest location. Immediate Impact: Your experience will directly influence Medpace's growth in the region. Career Growth: As the office grows, leadership and advancement opportunities will also increase. Global Reach: Work on cutting-edge clinical trials with international teams and top-tier sponsors. Strong Culture: Join a company known for its stability and commitment to professional development. Support & Infrastructure: While the Hyderabad office is new, you will be backed by the global resources and processes of a well-established CRO. If you are looking for a new challenge and want to be part of building something meaningful while advancing your career with a company that's investing in your region, we would love to hear from you. Responsibilities - Develop and review Data Management procedures for clinical trials with sponsor companies and other departments. - Establish/negotiate Data Management project timelines and ensure Data Management milestones are met. - Coordinate data transfers with the clinical database programmers, Project Manager, and external recipients. - Coordinate system development and ongoing maintenance in collaboration with the MCL programmers and MCL operational team. - Serve as the primary contact for MCL team members, sponsors, and external data management groups. Qualifications - Bachelor's degree with at least 7 years of Data Management experience in clinical research, prior experience in Core Lab preferred. - Experience in setting up and managing multiple clinical projects and acting as the main point of contact for the sponsor. - Computer experience with EDC databases and analysis software. - Possess an understanding of database structure and processes in data management. - Basic knowledge of medical terminology is needed, as well as knowledge of clinical research methodologies. Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through a scientific and disciplined approach. With headquarters in Cincinnati, Ohio, we employ more than 5,000 people across 40+ countries. Why Medpace People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. Medpace Perks - Flexible work environment - Competitive compensation and benefits package - Competitive PTO packages - Structured career paths with opportunities for professional growth - Company-sponsored employee appreciation events - Employee health and wellness initiatives Awards - Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023, and 2024 - Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility What To Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.,

As a Senior Medical Writer at Syneos Health, you play a vital role in leading the clear and accurate completion of medical writing deliverables. Your responsibilities include managing medical writing activities associated with individual studies, coordinating these activities within and across departments with minimal supervision. You will be responsible for completing various documents such as clinical study protocols, reports, patient narratives, annual reports, and more. Adhering to established regulatory standards, including ICH E3 guidelines, company standard operating procedures, and client standards, is essential. Your role involves coordinating quality and editorial reviews, ensuring proper management of source documentation. As a peer reviewer for the internal team, you will ensure document scientific content, clarity, overall consistency, and proper format. Interacting and building good working relations with clients, department heads, and peers in various departments are crucial for producing high-quality writing deliverables. In addition to these responsibilities, you will mentor and lead less experienced medical writers on complex projects, developing deep expertise on key topics in the industry and regulatory requirements. Working within budget specifications for assigned projects while maintaining a high level of quality is a key aspect of your role. To qualify for this position, you should have a Bachelor's degree in a relevant discipline with relevant writing experience, while a graduate degree is preferred. 4-5 years of relevant experience in a disclosure platform and strong understanding of FDA and ICH regulations are necessary. Proficiency in MS Office, strong project and time management skills, and a good grasp of medical terminology and principles of clinical research are also required for this role. At Syneos Health, you will have the opportunity to work in a dynamic and challenging environment where you can make a difference. Join us in our mission to accelerate the delivery of therapies and change lives.,

As an Associate Director, Study Site Engagement at Takeda, you will play a key role in enhancing engagement and providing added value by establishing and nurturing long-term relationships with investigators and study site personnel. You will support study teams with trial operations from Feasibility through CSR within the assigned region or countries across Takeda therapeutic areas. Your responsibilities will include supporting country and site identification, feasibility, site selection, study recruitment strategies, and mitigating barriers at the direction of Clinical Programs. You will be responsible for Study Specific Engagement activities, such as early engagement for country and site feasibility, supporting the development of study site lists for feasibility, attending Pre-Study Visits, tracking start-up hurdles, supporting recruitment strategy and activities, and ensuring compliance with applicable local regulations and SOP trainings. Additionally, you will interact closely with local CRO teams throughout the lifecycle of the study and attend Investigator Meetings as required. In addition to study-specific activities, you may also be involved in Non-Study Specific Engagement activities, such as people management, establishing communication with regional/country Medical Affairs, and participating in SSE Program Lead and/or SSE Study Lead roles for assigned programs. You may also be responsible for developing and maintaining long-term strategic relationships with selected sites to improve the site and Takeda experience. To qualify for this role, you should have a scientific degree in pharmaceutical science, chemistry, biology, or healthcare, with 10+ years of experience in clinical research. You should have advanced knowledge of clinical trials processes, regulations, and ICH-GCP, as well as strong communication and influencing skills. Fluency in spoken and written English is required. This position is field-based with monthly visits to the Takeda Delhi/Mumbai office, and travel in the assigned region may be required up to 40% during busy periods. If you are looking for a patient-focused company that empowers its employees to work towards their potential and make a difference in the healthcare industry, Takeda could be the right place for you to take charge of your future and contribute to our inspiring mission of delivering Better Health and a Brighter Future to people around the world.,

Job Description: We are hiring a Radiologist for a reputed Diagnostic Centre located in Alwal, Hyderabad . The ideal candidate should be proficient in handling and interpreting diagnostic imaging including USG, CT, and MRI . Key Responsibilities: Perform and interpret Ultrasound, CT Scan, and MRI Provide accurate diagnostic reports in a timely manner Collaborate with referring physicians for clinical correlation Maintain imaging protocols and ensure patient safety standards Support in maintaining radiology equipment and quality standards Requirements: MBBS with MD/DNB/DMRD in Radiology Valid medical council registration Good diagnostic skills and ability to handle high patient volumes Strong communication and teamwork skills Akash HR Manager [HIDDEN TEXT] || 90 637 637 34

As a Manager, Medical Writing & Research Affairs at TECCRO, you will play a crucial role in preparing high-quality scientific documents, including clinical study reports, research papers, regulatory submissions, and publications for medical journals. Your responsibilities will involve collaborating closely with clinical and research teams to ensure that manuscripts meet publication standards for major medical journals and align with the latest scientific research and TECCRO's clinical objectives. Your role will also require you to conduct thorough literature reviews, contribute to the design of clinical trials, and stay updated with current scientific and clinical advancements in the fields of medical aesthetics, skincare, and clinical trials. Additionally, you will work closely with internal teams, including clinical researchers, data managers, and regulatory affairs, to support the alignment of documents with clinical objectives and regulatory standards. Your expertise in medical writing will be essential for supporting business development efforts, including proposal creation and client communication. You will also assist in the preparation of regulatory submissions, ensuring that scientific documents align with required formats and regulatory guidelines. To excel in this role, you should possess exceptional writing, editing, and proofreading skills with a meticulous attention to detail. A strong understanding of clinical research methodologies, regulatory guidelines, and Good Clinical Practices is required. Proficiency in using writing and reference management software, along with excellent collaboration skills, will be beneficial for effectively working across cross-functional teams. If you are a skilled medical writer with a passion for science and research, this role offers an exciting opportunity to contribute to the advancement of clinical research and academic publications within the growing field of medical aesthetics. TECCRO provides a competitive salary with performance-based incentives, opportunities for professional development, certifications, and career growth, along with a supportive and collaborative work environment focused on research excellence and innovation in clinical trials. Join us at TECCRO and be a part of driving scientific and technological innovation in the aesthetics industry!,

You will be responsible for leading scientific engagement with Medical Experts as the MSL Manager. In this role, you will implement clinical and educational strategies, as well as respond to unsolicited medical inquiries. Your key responsibilities will include building and maintaining scientific relationships with Medical Experts, identifying key accounts aligned with medical priorities, developing engagement plans tailored to country-specific strategies, and providing accurate scientific information in response to medical inquiries. Additionally, you will support clinical trial execution, facilitate Investigator Initiated Trial processes, act as a scientific resource for internal field teams and partners, and ensure timely reporting of adverse events and product complaints. To excel in this role, you must have proven experience in operations management and cross-functional collaboration, a strong understanding of clinical research and medical affairs processes, proficiency in scientific communication including medical writing and data interpretation, familiarity with CRM tools and digital platforms for stakeholder engagement, knowledge of disease management, drug development, and epidemiology, and the ability to analyze and present clinical data effectively. Fluency in English, both written and spoken, is essential. Desirable requirements include prior experience in a Medical Scientific Liaison or similar field-based medical role, as well as an advanced degree in life sciences such as MD, PhD, or PharmD. Novartis is committed to creating an inclusive work environment and diverse teams that represent the patients and communities served. If you require any reasonable accommodation due to a medical condition or disability during the recruitment process, please reach out to [email protected] with the details of your request and the job requisition number. Join Novartis in reimagining medicine to improve and extend people's lives. Be part of a community of smart, passionate individuals collaborating, supporting, and inspiring each other to achieve breakthroughs that positively impact patients" lives. Visit https://www.novartis.com/about/strategy/people-and-culture to learn more about our mission and opportunities.,

Job Description As a pioneer in Healthcare, Manipal Hospitals is among the top healthcare providers in India serving over 5 million patients annually. Today we stand as an integrated network with a pan-India footprint of 37 hospitals across 19 cities with 10,500 beds, and a talented pool of over 5,600 doctors and an employee strength of over 20,000. Role: Associate -Clinical Pharmacist Location: Dwarka, Delhi What You'll Do: Conduct medication reviews and assessments to ensure appropriate pharmacotherapy for patients. Collaborate with physicians and healthcare teams to develop individualized treatment plans. Provide drug information and education to patients and healthcare staff regarding medication use, dosing, and side effects. Monitor patient responses to therapy and make recommendations for therapy adjustments as necessary. Participate in clinical rounds, case conferences, and interdisciplinary meetings to advocate for safe medication practices. Conduct therapeutic drug monitoring and adjust medications based on clinical guidelines and patient needs. Participate in the development and implementation of pharmacy-related policies and protocols. Stay updated with the latest advancements in pharmacotherapy and clinical guidelines. Mentor and train junior staff and pharmacy students as required. Ensure compliance with regulatory requirements and quality assurance standards. What We Are Looking For: Doctor of Pharmacy (Pharm.D.) or equivalent degree from an accredited institution. Active Pharmacy license in the practicing state. Previous experience in a clinical pharmacy setting is preferred. Strong knowledge of pharmacology, therapeutics, and medication management. Excellent communication and interpersonal skills. Ability to work collaboratively in a multidisciplinary team environment. Strong analytical and problem-solving skills. What We Offer: Competitive salary and benefits package Opportunities for professional development and career growth A collaborative and inclusive work environment Mandatory Skills Pharmacovigilance, Clinical Research, Clinical Data Management, Clinical Operations Location Delhi Roles & Responsibilities As a pioneer in Healthcare, Manipal Hospitals is among the top healthcare providers in India serving over 5 million patients annually. Today we stand as an integrated network with a pan-India footprint of 37 hospitals across 19 cities with 10,500 beds, and a talented pool of over 5,600 doctors and an employee strength of over 20,000.

The position of Global Medical Advisor in the Medical Affairs department at Novo Nordisk involves providing strategic and medical guidance for a portfolio of products. As a part of the APAC Medical Affairs team, you will play a crucial role in various aspects such as the PDP process, interpretation and communication of scientific data, and understanding the clinical importance of new findings related to diabetes, obesity, rare diseases, and OSCD. Your responsibilities will include acting as the PDP Secretary, driving the PDP process at the regional level, and ensuring the timely and accurate delivery of scientific medical guidance to internal and external stakeholders. You will also be responsible for managing effective collaboration within the APAC medical affairs team, acting as a liaison between Novo Nordisk and Key Opinion Leaders, and ensuring the application of Novo Nordisk policies and procedures. Additionally, you will be involved in developing and maintaining relationships with Global Key Opinion Leaders, planning and executing meetings, supporting speakers in presenting data at conferences, and engaging in scientific dialogue to advance the company's products. Your role will also entail providing medical guidance, developing medical documents and digital solutions, and supporting key markets and affiliates through training and education. The ideal candidate for this position should hold an M.D. with substantial clinical and/or research expertise in relevant areas such as Endocrinology, Cardiology, General Practice, or Internal Medicine. Strong clinical and/or research background in diabetes mellitus, experience in drug development, and fluency in English are essential qualifications. Demonstrated research experience, at least 2 years of clinical and/or pharmaceutical industry experience, and familiarity with clinical research and development are also required. Joining the Global Medical Affairs team at Novo Nordisk in Bangalore means becoming part of a motivated group of global scientific advisors, project managers, and publication managers working together to communicate scientific and medical knowledge on company products. As a leading global healthcare company dedicated to defeating serious chronic diseases, Novo Nordisk offers a collaborative and inclusive work environment where employees are encouraged to bring their unique skills and perspectives to the table. If you are passionate about making a difference and contributing to life-changing initiatives, we invite you to apply by submitting your CV and motivational letter online before the deadline of 28th February 2025. Novo Nordisk is committed to an inclusive recruitment process and equality of opportunity for all job applicants, and we do not extend unsolicited employment offers or charge fees to prospective employees. Our goal is to be the best company for the world, and we believe that diversity and inclusion are essential to achieving this vision. Together, we are life changing.,

As a Clinical Research Associate based in Bhubaneshwar, your primary responsibilities will include performing site feasibility assessments, identifying potential investigators, negotiating study budgets, finalizing investigators and sites, and executing CDA and study-related contracts. You will also be responsible for preparing and submitting study documents for EC permission across centers, overseeing IP dispensing, managing inventory, and conducting reconciliations. In addition, you will play a key role in ensuring timely site initiation, monitoring, and close-out activities, as well as overseeing investigator and site personnel training on study protocols, procedures, and GCP principles. Your duties will also involve facilitating the recruitment of trial participants, ensuring efficient data entry, source data verification, and query resolution, and reporting SAEs and SUSARs in compliance with regulations and Suns PV policies. Furthermore, you will be responsible for identifying risks, conducting analysis, and implementing CAPA for sites that do not meet expectations. Collaborating with in-house or CRO partners for data management, statistical analysis, and report generation will also be part of your role. To qualify for this position, you must have a Bachelor's or Master's degree in a health-related field such as Biology, Chemistry, Nursing, Pharmacy, or Public Health. A Post-graduate Diploma in Clinical Research would also be beneficial. Additionally, a minimum of 1-5 years of relevant experience in Clinical Research is required to be successful in this role.,

Join Amgen's Mission to Serve Patients If you feel like you're part of something bigger, it's because you are. At Amgen, our shared mission to serve patients drives all that we do. It is key to our becoming one of the world's leading biotechnology companies. We are global collaborators who achieve together, researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It's time for a career you can be proud of. What You Will Do The Scientific Communications Senior Manager is accountable for planning and delivering innovative scientific and medical content aligned to their designated Therapeutic Area/product (General Medicine, Inflammation, Oncology, Rare Disease, or Obesity), tailored to specific audiences globally via impactful formats and relevant channels. Reporting to a Scientific Communications Therapeutic Area (TA) Lead in India, this leader manages a small team of scientific communication team members and drives the execution of tactical Scientific Communication plans for US and global regions to deliver our Medical and overall product strategies. The Scientific Communications Senior Manager may directly partner with US/Regional Medical planning team and Scientific Communication Operations team members to drive process alignment, standardization, and adoption of innovation and transformational change. This role is responsible for creating and leading high-performing and engaged teams to exceed expectations. Roles And Responsibilities - Develop and deliver high-quality, accurate, and innovative scientific and medical content (DSE/digital/MSL materials/FAQs/Medical Information Letters) tailored to specific audiences in the US and globally via impactful formats and relevant channels. - Publication-related deliverables (manuscripts/abstracts/posters/Oral presentations, enhanced content). - Addressing Medical Information inquiries/issues. - Maintain strong partnerships with Scientific Communication Operations team in support of standardization of processes, optimizing systems, and furthering continuous improvement and innovation, including the use of digital and multi-channel approaches, as well as definition of impactful KPIs. - Drive the execution of a comprehensive scientific communication plan that shifts based on changes in the disease area and treatment landscape and in-depth awareness of insights across local affiliates and cross-functional partners. - Ensure compliance with relevant Amgen enterprise and Functional SOP(s) and system(s). - Assist in recruiting, onboarding, and training of staff members. - Support prioritization process, prepare and oversee team assignments to meet program goals on time and within budget. - Develop, maintain, cultivate, and influence strong relationships with cross-functional colleagues. - Foster Amgen culture and motivate high-performing and empowered staff. What We Expect Of You We are all different, yet we all use our unique contributions to serve patients. Basic Qualifications - Doctorate degree with a minimum of 10 years of experience in Global Publication, Medical Communications, Medical Value and Access, or Medical Strategy. - Masters degree with a minimum of 12 years of experience. - Bachelors degree with a minimum of 14 years of experience. - Minimum of 5 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources. Must-Have Skills - MD, PharmD, PhD, or DO with 4 or more years of expertise in clinical research, patient care, Clinical Development, Medical/Scientific Affairs, and/or basic research (other doctorate degrees may be considered). - Prior experience in Medical/Scientific Affairs or Clinical Development within the biopharmaceutical industry, and/or clinical or research in the therapeutic area. - An understanding of the pharmaceutical commercialization process and knowledge of the regulatory and legal guidelines affecting promotion of prescription products. - Experience in publication planning, publications guidelines, and transparency standards (e.g., ICMJE, current Good Publication Practice (GPP) Guidelines). - Understanding of Amgen focused disease area and landscape and clinical data to enable critical analysis of scientific literature and communicate implications cross-functionally. - Demonstrated track record of strategic execution in a matrix environment with limited supervision. - The ability to work in teams and interface in a dynamic environment across corporate functions. Preferred Skills - Knowledge of emerging technologies in medical communications (e.g., AI tools, omnichannel engagement platforms). - Strong computer and database skills, particularly with Microsoft Office products. Soft Skills - Strong verbal and written communication skills. - Ability to work effectively with global, virtual teams. - High degree of initiative and self-motivation. - Ability to manage multiple priorities successfully. - Collaborative mindset with a strong sense of accountability and ownership. - Ability to drive continuous improvement and adapt quickly in a fast-evolving environment. - Strong project management with the ability for self-direction. What You Can Expect Of Us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we'll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now for a career that defies imagination. Objects in your future are closer than they appear. Join us. EQUAL OPPORTUNITY STATEMENT We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.,

Join Marbles Health in revolutionizing the future of brain health. We are dedicated to enhancing brain and mental health through innovative approaches and cutting-edge technology. Our team of neuroscientists, engineers, and clinicians has developed India's first medically approved brain stimulation device for various conditions such as depression, anxiety, and addiction. As a Clinical Researcher at Marbles Health, you will play a pivotal role in advancing the field of behavioral science, psychology, and neuroscience. You will be at the forefront of clinical research and technology-driven therapeutics, shaping the future of digital interventions and brain stimulation protocols. Your key responsibilities will include designing and leading Randomized Controlled Trials (RCTs) and pilot programs, serving as the scientific lead on clinical protocols, and developing case studies that redefine standards in cognitive and behavioral science. You will lead translational research efforts, bridging the gap between theoretical hypotheses and real-world impact. Collaborating with a multidisciplinary team, you will contribute to the development of digital cognitive modules that are clinically informed and user-friendly. Additionally, you will represent Marbles Health in research and clinical communities, contributing to academic conferences and collaborations with public/private institutions. To excel in this role, you should hold a Masters, M.Phil., or PhD in Clinical Psychology, Neuropsychology, Cognitive Neuroscience, or a related field. You should have 1-3 years of experience in clinical trials, mental health research, or within high-growth startups. Deep understanding of behavioral science, cognitive intervention design, and hands-on experience in experimental design are essential. Excellent academic writing skills and familiarity with research tools and digital health platforms are highly valued. This is not just a research role; it's an opportunity to be on the frontier of where science meets patient care. You will be part of a founding team creating a new therapeutic category in India and beyond. You will have a direct influence on product strategy, collaborate with a team of innovators, and work towards making breakthrough brain health accessible to millions. If you are passionate about making a tangible impact in the field of brain health and want to be part of a dynamic team, we invite you to apply now and be a part of reshaping the future of mental health care.,

We are seeking an expert MSL-Oncology Consultant to represent Company's Medical Affairs as a subject matter expert in Oncology. You will provide scientific and technical leadership, developing credible relationships with external experts and healthcare professionals, and serving as a key point of contact for scientific knowledge. This role involves developing and executing scientific interaction plans, facilitating research initiatives, and supporting internal teams with scientific updates, all while ensuring strict compliance. Roles and Responsibilities: Represent Company's Medical Affairs as a subject matter expert in Oncology and the assigned territory, providing scientific and technical leadership to ensure professional and credible relationships with external experts /HCPs of strategic importance to Company. Serve as a point of contact within the Medical Affairs team for external experts within an assigned geographic area to satisfy their needs for scientific knowledge in the assigned therapeutic area and, when requested, relevant medicines, to support their safe, effective, and appropriate use. Develop and execute scientific interaction plans and cycle plans; contribute to cross-functional account planning, as appropriate. Responsible for appropriate tiering and segmentation of external experts based on guidance from the IFT playbooks and appropriate documentation of HCP interactions and relevant insights in the Veeva CRM and related platforms and systems. Ensure a strong medical and scientific presence for Company in key academic centers by facilitation of research and educational initiatives , while supporting requests for medical and scientific information on products or areas of therapeutic interest to Company. Support internal teams such as sales and marketing and members of the Affiliate Brand Team to develop their scientific and technical expertise through the delivery of scientific update presentations. Work collaboratively and cross-functionally with other in-field members while retaining functional independence. Assist in the initiation, oversight, and follow-up of assigned GMA studies and medical projects initiated within the therapeutic area for which the MSL carries responsibility (e.g., registry/database projects, epidemiological studies, post-authorization studies (PMOS), where applicable). Support prioritized interventional studies run by Clinical Development Operations, with study initiation visits, and act as subject matter expert, where applicable, as part of One R&D community. All such activities must comply with applicable local laws, guidelines, codes of practice, SOPs, and R&D SOPs. Ensure that all activities and interactions are conducted with due regard to all applicable local, global, and national laws, regulations, guidelines, codes of conduct, Company policies, and accepted standards of best practice. Skills Required: Solid knowledge of the pharmaceutical environment and the role of Medical Affairs to advance the medical and scientific objectives of a pharmaceutical company. Demonstrated expertise in the scientific methods applied to clinical research and current legislative/regulatory controls applicable to this research will be an added advantage. Ability to comprehensively learn about new subject areas and environments. Excellent written and spoken communication and presentation skills , with a demonstrated ability to develop and maintain strong collaborative relationships with thought leaders, physicians, and other healthcare decision-makers. A good understanding of written and oral English is a must. High customer orientation. Strong commitment to compliance with the relevant rules and procedures, and to scientific quality and integrity. QUALIFICATIONS: MBBS and MD (Preferable). Candidates with an undergraduate degree with relevant years of experience will be considered.

Help bring cutting-edge medical treatments to life by becoming a key player in clinical research and accelerating advancements in healthcare. Explore two pathways into the dynamic world of clinical research: Internship: Embark on a hands-on introduction to clinical trials through a structured internship program. This opportunity is ideal for students or recent graduates eager to gain valuable experience in the field. Fresher-Level Position: Kickstart your career as a Clinical Research Coordinator! This position provides continuous employment for individuals dedicated to this exciting field. Regardless of the chosen path, you will have the opportunity to: - Manage the flow of clinical trials: Oversee study logistics, participant documentation, and ensure seamless progress in the study. - Maintain meticulous records: Collect and safeguard essential research data adhering to the highest industry standards. - Advocate safety and ethics: Safeguard patient rights and ensure all research practices comply with ethical standards. - Collaborate with a team of professionals: Work closely with investigators, healthcare providers, and fellow research enthusiasts. Qualifications: Internship: Enrolled in or a recent graduate of a degree program in life sciences, health sciences, nursing, or a related field. Fresher-Level Position: Recent graduate with a degree in life sciences, health sciences, nursing, or a related field. For both roles, a passion for research, attention to detail, strong organizational skills, effective communication, and a willingness to learn are essential. What We Offer: - Hands-on experience: Jumpstart your career or gain real-world training. - Training and mentorship: Receive guidance from experienced researchers in the field. - Professional development: Access resources and company-sponsored coursework to enhance your skills. - Competitive compensation: Interns receive a stipend; fresher-level positions offer a salary and benefits package. - A role at the forefront of medical innovation: Contribute to shaping the future of healthcare through your work in clinical research.,

Description We are seeking an experienced Clinical Trials professional to manage and oversee clinical research studies in India. The ideal candidate will have a strong background in clinical trial design and execution, ensuring compliance with regulatory standards and the safety of trial participants. Responsibilities Design and implement clinical trial protocols in compliance with regulatory standards. Monitor trial progress and ensure adherence to timelines and budgets. Coordinate with various stakeholders, including sponsors, regulatory authorities, and clinical sites. Collect, analyze, and interpret data from clinical trials. Prepare and submit regulatory documents and reports. Train and supervise clinical trial staff and investigators. Ensure the safety and well-being of trial participants. Skills and Qualifications 6-16 years of experience in clinical trials or related field. Strong understanding of Good Clinical Practice (GCP) and regulatory requirements. Proficiency in clinical trial management software and electronic data capture systems. Excellent organizational and project management skills. Strong analytical and problem-solving abilities. Effective communication and interpersonal skills. Ability to work collaboratively in a team environment.

Are you passionate about Clinical Research and eager to gain hands-on experience Neo Genesis Clinical Research is offering a 3-month UNPAID INTERNSHIP for enthusiastic individuals ready to learn and contribute to meaningful research projects in the heart of the capital. Internship Requirements: - Basic knowledge or academic background in Clinical Research. - Ability to work effectively in a team. - Capable of meeting strict deadlines. Preferred Qualifications: - Pursuing or recently completed a Bachelors or Masters degree in Biotechnology, Biochemistry, Microbiology, Pharmacy, Bpharma, Mpharma, or other Life Sciences fields. - Freshers are welcome to apply and gain valuable industry experience. IT Skills: - Proficiency in MS Word and Excel. Location: - New Delhi If you're ready to take your first step in Clinical Research, send your resume to neogenesiscr@gmail.com or DM us for more details.,

The Associate Clinical Development Director (Assoc. CDD) plays a crucial role in contributing to the development of protocols for assigned global clinical trials, monitoring scientific aspects, and ensuring the reporting of high-quality data. Depending on the size and complexity, they may also provide support in developing the clinical and scientific strategy for specific sections of a clinical development program. Their responsibilities encompass overseeing all operational aspects of clinical trials, from planning and execution to interpreting research findings and managing data collection activities and clinical operations. Additionally, they are responsible for complete oversight of budget and resource allocation within the assigned trial, driving operational excellence through process improvement and knowledge sharing across trials within the program or franchise. The Associate Clinical Development Director serves as a point of escalation for resolving operational issues within the assigned trial. In their role, the Associate Clinical Development Director is tasked with providing input to the development of clinical development strategy, contributing to the development of trial-related documents, and collaborating with the appropriate Clinical Trial Team (CTT) members. They conduct ongoing scientific reviews of clinical trial data, manage patient safety reports, provide input into final analyses and interpretations, and contribute to global initiatives for process improvement and other line function activities. The Associate Clinical Development Director may also lead clinical trials as a Clinical Scientific Lead, providing leadership and guidance for all clinical aspects of the trial in collaboration with the medical monitor and/or Clinical Development Director. Key Performance Indicators for the role include demonstrating quality clinical and scientific strategic input, applying effective clinical research methodology, supporting Therapeutic Area (TA) through high-quality contributions, and ensuring timely development of disease/program clinical standards, publications, and presentations. The Associate Clinical Development Director is expected to excel in executing and implementing clinical operations strategy, managing budget and resources effectively, and demonstrating strong leadership skills to support team competency building and best practice sharing across programs and departments. Clear communication of risks, cost-effective management, and adherence to Novartis Values and Behaviors are also essential aspects of the role. Minimum Requirements for the position include a preference for Neuroscience or similar experience, an advanced degree in life sciences or healthcare, and at least 3 years of involvement in clinical research or drug development in an academic or industry environment. The ideal candidate should have a working knowledge of clinical trial design and methodology, statistics, regulatory processes, and strong communication and interpersonal skills. Proficiency in budget management, clinical research, coaching, cross-functional teamwork, and risk management is also necessary. Language requirements for the role include proficiency in English. Novartis offers a collaborative environment for individuals passionate about making a difference in patients" lives through innovative science. If you are ready to contribute to creating a brighter future, consider joining the Novartis Network to explore career opportunities and benefit from a supportive community focused on personal and professional growth.,

You will be working as a Clinical Project Manager (CDM) with 8 to 15 years of experience. The current locations where the job is available include Hyderabad, Bangalore, and Mumbai, but the preference location is Hyderabad. Your primary work location will be in Hyderabad with a hybrid working model. Your main duties will involve managing one or more projects with a focus on timely delivery, staying within budget, and ensuring high-quality outcomes. You will be required to support Project Managers in project delivery, track study deliverables, manage client expectations, monitor project scope, timelines, budget, milestones, issues, and risks. Additionally, you will be responsible for monitoring project financials, budget tracking, accuracy of invoicing, maintaining study documentation, raising work requests to other departments, capturing minutes/action items during meetings, tracking problems/issues, ensuring timely resolutions, proactively communicating with stakeholders, and ensuring compliance with project management methodologies and SOPs. As for the required skills and qualifications, you should have a basic understanding of clinical research in pharma, device, and/or biotech sectors, as well as Clinical Research SaaS technology. Good verbal and written communication skills, organizational skills, time management, collaboration, team-building awareness, experience in supporting project teams, and meeting project timelines are essential. Being self-motivated, professional, proficient in EDC/CDM systems, having computing skills, experience with MS Office suite (Word, Excel, PowerPoint), and presentation skills will be beneficial for this role.,

As an employee at Advarra, you will be part of a passionate team dedicated to making a difference in the world of clinical research and advancing human health. With our rich history in ethical review services and innovative technology solutions, we are leading the industry in breaking down barriers and accelerating trials. Your role will be crucial in developing and maintaining internal budgets for clinical trial sites, negotiating budgets with sponsors and CROs, and ensuring compliance with regulations and industry best practices. You will play a key role in the development and approval of internal budgets, redlining budgets based on coverage analyses for new studies, and capturing all necessary fees and services required for the study. Negotiating clinical trial budgets on behalf of sites, discussing budgets with study teams and sponsors, and ensuring alignment and agreement will also be part of your responsibilities. Your analytical abilities will be put to the test as you manage a diverse portfolio of clinical trial protocols, ensuring compliance with regulations and liaising between US and India teams. Training, developing, and mentoring budget analysts, overseeing team activities, and managing escalations related to budget issues will be essential for team development. You will also contribute to strategic planning, define service scaling, and act as a thought leader in the industry to promote Advarra services. Quality control, compliance, liaison between teams, and process development will be areas where your expertise will be invaluable. Additionally, participating in project teams, monitoring key performance metrics, and providing analytical insights will be part of your regular duties. To be successful in this role, you should have a Bachelor's degree in a relevant field, 5+ years of experience in clinical research budget development, negotiation skills, and familiarity with FDA and Medicare regulations. Preferred qualifications include advanced degrees, experience with clinical trial management systems, and exceptional analytical, communication, and negotiation skills. Your attention to detail, leadership capabilities, and ability to manage team escalations will be critical in ensuring the success of our clinical trials. This position is open to candidates working in a hybrid model in Bengaluru, Karnataka, India. If you are looking to join a dynamic team committed to advancing clinical research and improving patient outcomes, this role at Advarra may be the perfect fit for you.,

You will be responsible for architecting and delivering Automation and AI solutions using cutting-edge technologies, with a strong focus on foundation models and large language models. Working closely with business stakeholders, you will understand business requirements and design custom AI solutions to address complex challenges. This role offers the opportunity to accelerate AI adoption across the business landscape in the Statistical Applications and Data domain. Your key responsibilities include defining and leading AI use cases in clinical projects from start-up through close-out. This involves tasks such as protocol development, site management, and data review. To excel in this role, you must be a proficient programmer capable of developing AI solutions thoroughly. Additionally, you will be expected to coach and mentor junior AI/ML engineers to enhance and accelerate AI adoption in business processes. Required Technical Skills: - Bachelors degree in a relevant scientific discipline (e.g., Biomedical engineering, Life Sciences, Nursing, Pharmacy) or clinical background (e.g., MD- Doctor of Medicine OR RN - Registered Nurse) - Advanced degree (e.g., Masters or Ph.D.) in Data Science, AI/ML - Overall experience of 10-12 years with a minimum of 5-7 years in clinical research, particularly managing clinical trials in pharmaceutical, biotechnology, or contract research organization (CRO) settings - Minimum of 5-7 years of experience in AI research and development, specifically focusing on healthcare or life sciences applications - Strong understanding of clinical trial regulations and guidelines, including Good Clinical Practice (GCP), International Conference on Harmonization (ICH), and applicable local regulations - Proven track record in designing and delivering AI solutions, emphasizing foundation models, large language models, or similar technologies - Experience in natural language processing (NLP) and text analytics is highly desirable - Proficiency in programming languages such as Python, R, and experience with AI frameworks like TensorFlow, PyTorch, or Hugging Face - Knowledge of libraries such as SciKit Learn, Pandas, Matplotlib, etc. - Familiarity with cloud platforms (e.g., AWS, Azure, GCP) and related services is a plus - Experience working with large datasets, performing data pre-processing, feature engineering, and model evaluation - Proficiency in solution architecture and design, translating business requirements into technical specifications, and developing scalable and robust AI solutions In summary, this role requires a seasoned professional with a strong background in AI, clinical research, and technical expertise to drive innovation and AI adoption in the pharmaceutical domain, particularly in clinical settings.,

Serve in support level capacity in CDM Validation (Testing) team, to perform testing activities in CDMS environment to provide efficient, quality database as per customer requirement. Essential Functions Conduct testing activities to validate Edit Checks, SAS listings, Transfer programming and custom reports in platforms like InForm, RAVE, OCRDC and/or Oracle Clinical. Basic understand database structures. Understand the documentation requirements and update all relevant documents in a timely manner. Understand and comply with Standard Operating Procedures and Work Instructions (including Best Practice and Guidance documents). Meet project objectives as assigned by the Validation Team Lead or Manager. Escalate problems to the attention of the Validation Team Lead or Manager. Develop and maintain good communications and working relationships within the team. All responsibilities are essential job functions unless noted as nonessential (N). Qualifications Bachelors Degree Bachelor in Science/Computer science/Information Technology or Bachelor in Technology Req 0-1 years of relevant clinical DB Testing experience in CDMS Platforms Req IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs. iqvia. com

The objective of this position is to provide medical expertise in the evaluation of safety data from a variety of sources as part of the overall pharmacovigilance process and determine the medical and scientific relevance of serious adverse event reports within the context of the product s safety profile as well as other products within the same therapeutic area. Also, this position plays a greater role as a senior technical leader and participate in matrix management activities including preparation or participation in evaluating safety issues and preparation of aggregate reports in collaboration with the Post-Marketing Safety Experts and Safety Surveillance Group and be responsible for surveillance activities for selected products. Essential Functions Perform medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative content, queries, coding, expectedness, seriousness, causality and company summary Compose, edit and medically review Analyses of Similar Events (AOSE) for expedited cases as appropriate based on regulatory requirements Provide coding review of AEs, SAEs, SADRs, Past medical history, Concomitant medications or other medical data listings to verify and medically vet clinical data Serve as an internal consultant to pharmacovigilance case processing teams on projects being supported Perform medical safety review of the protocol, Investigative Brochure, and/or Case Report Forms (CRFs) for appropriate safety content and data capture, as applicable Provide aggregate reviews of safety information, including but not limited to clinical data, postmarketing, literature review and observational studies to maintain oversight of a product s safety profile (e. g: DSUR, RMP, PBRER, ad hoc regulatory reports etc) Ensure service delivery from productivity, compliance and quality perspective within regulatory /contracted timelines. Lead and participate in the initiatives taken for the same from team delivery perspective Provide therapeutic area/pharmacovigilance issue guidance in the context of leading/managing other safety team members in single case assessment. Ensure update of watch list, list of expectednsess, labeling list/RSIs etc for the assigned products and develop such additional capabilities within the team Lead, drive and participate in training activities, product transitions, audit preparation and knowledge exchange initiatives Review and sign off on the Project Safety Plan and Medical Monitoring Plan per medical safety scope agreed in contract, as applicable Attend project meetings, medical safety team meetings, and represent safety and clinical data review findings during client meetings, as applicable Act as Lead Safety Physician, or additional team support, and/or back up on assigned projects as applicable Provide medical escalation support for medical information and EU Qualified Persons for Pharmacovigilance projects, as applicable 24 hour medical support as required on assigned projects Maintain awareness of medical safety-regulatory industry developments Provide support and participate in signal detection efforts, e. g. strategy meetings etc. as applicable Qualifications Other A medical degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education. Req Three (3 years) experience practicing clinical medicine after award of medical degree. Graduate, and/or Residency training can qualify for clinical practice experience Req Two (2) years of pharma experience Pref Sound knowledge of Medicine In-depth knowledge of applicable global, regional and local clinical research regulatory requirements; i. e. , Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Knowledge of Pharmacovigilance- ICSR and Aggregate reports In-depth knowledge of departmental standard operating procedures (SOPs) Skill in use of multiple safety databases Adequate Computer skills, especially Microsoft word, excel & PowerPoint Good communication skills- verbal and written Ability to establish and maintain effective working relationships with managers, co-workers, investigative site staff, clients and regulatory agency representatives Ability to establish and maintain effective working relationships with coworkers, managers and clients A valid medical license, or equivalent, from the country or region in which he/she resides and works Pref IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs. iqvia. com

Review, assess and process Safety data and information, across service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations SOPs and internal guidelines under guidance and support of senior operation team members. Essential Functions To Prioritize and complete the assigned trainings on time Process Safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs) and project requirements. To perform Pharmacovigilance activities per project requirement including but not limited to, collecting and tracking incoming Adverse Events(AE)/endpoint information determining initial/update status of incoming events database entry coding AE and Products, writing narratives, Literature related activities. Assuming other workflow responsibilities for the assigned project as directed by Operations team member or Manager. Ensure to meet the expected productivity and quality standards Ability to identify quality problems, if any, and bring them to the attention of a senior team member/ mentor. Attend project team meetings and provide feedback to operations manager on any challenges/issues or successes. 100% compliance towards all people practices and processes Perform other duties as assigned Qualifications High School Diploma or equivalent Scientific or healthcare discipline or allied life sciences An Individual with a minimum of a Bachelor s Degree in scientific or healthcare discipline or allied life sciences graduation. Good knowledge of medical terminology. Strong verbal/written communication skills. Ability to work as a Team Player, contribute and work towards achieving Team goals. Good working knowledge of Microsoft Office and web-based applications. Self-motivated and flexible. Attention to detail and accuracy. Ability to follow instructions/guidelines, utilize initiative and work independently. Ability to manage competing priorities and deadlines. Willingness and aptitude to learn new skills across Safety service lines. Strong time management skills. Ensure quality of deliverables according to the agreed terms. Demonstration of IQVIA core values while doing daily tasks - Extensive use of keyboard requiring repetitive motion of fingers. Extensive use of telephone and face-to-face communication requiring accurate perception of speech. Regular sitting for extended periods of time. May require occasional travel. Flexibility to operate in shifts. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs. iqvia. com