3711 Clinical Research Jobs - Page 48

At EY, you will have the opportunity to shape your future with confidence, succeed in a globally connected powerhouse of diverse teams, and take your career wherever you desire. Join EY to help build a better working world. As a Data Integration Architect with 8+ years of experience in clinical or life sciences domains, you will lead the integration of Medidata platforms into enterprise clinical trial systems. Your role will involve designing scalable, compliant data integration solutions, collaborating across global R&D systems, and contributing to data-driven innovation in the healthcare and life sciences space. You will play a crucial part in aligning integration efforts with organization...

Summary The Clinical Development Medical Director (CDMD) is the clinical leader of a section of a clinical program (e.g., an indication, a new formulation, or a specific development phase), or a large, complex trial, under the leadership of the (Sr.) GPCH. About The Role Your responsibilities include, but are not limited to: Provide clinical leadership and medical strategic input for deliverables in the assigned project/program. Deliverables may include sections of individual protocols consistent with the IDP, data review, program specific standards, clinical components of regulatory documents/registration dossiers, and publications (e.g., IBs, Brochures, briefing books, safety updates, subm...

As a Clinical Research (CRA) Manager at Medpace in Navi Mumbai, India, you will play a crucial role in our growing clinical operations activities. Your primary responsibility will be the effective management of Clinical Research Associates (CRAs) to ensure the smooth functioning of clinical trial processes. Your key responsibilities will include: - Line management of CRAs, overseeing their recruitment, initial and ongoing training, and development - Ensuring that CRAs meet the core monitoring responsibilities and expectations - Tracking and managing CRA resourcing and allocation of assignments - Managing turnover and retention of CRAs in alignment with company objectives To excel in this rol...

As the Medical Scientific Expert for the assigned product(s) and relevant therapeutic areas, your role will involve providing expert advice and guidance to healthcare professionals. You will play a key role in facilitating information, education, and research activities for physicians and ancillary healthcare professionals, focusing on current and future therapies in development or already commercialized. Your responsibilities will include engaging in scientific exchange and developing professional relationships with key opinion leaders. Additionally, you will be expected to provide medical scientific input into marketing strategies and key commercial initiatives. To excel in this role, you ...

In this vital role, you will be responsible for developing and maintaining the enterprise architecture vision and strategy for the Clinical Computation Platform, ensuring alignment with business objectives. The ideal candidate will be a leader in architecture, with a strong background in designing scalable, secure, and resilient IT systems. You will work closely with partners to translate requirements into robust solutions and drive continuous improvement through innovation and the evaluation of emerging technologies. Roles & Responsibilities Architecture Strategy & Governance: Develop and maintain the enterprise architecture vision and strategy, ensuring it aligns with business objectives. ...

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 ht...

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 sh...

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 Gro...

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...

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 f...

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...

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 ...

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 team...

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 me...

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 respo...

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. ...

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, Onc...

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 respo...

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 ...

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:...

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...

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 experien...

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 budge...

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 monitorin...