1999 Clinical Trials Jobs - Page 23

Description We are seeking a highly organized and detail-oriented Schedule Y to join our team in India. The ideal candidate will play a crucial role in managing project timelines and ensuring the successful execution of projects. Responsibilities Develop and implement project schedules using appropriate software tools. Monitor project timelines and ensure adherence to deadlines. Collaborate with project teams to update schedules and communicate changes. Identify potential scheduling conflicts and propose solutions. Prepare and present schedule reports to stakeholders. Skills and Qualifications Proficiency in project scheduling software (e.g., MS Project, Primavera). Strong analytical and pro...

As a Manager of Biostatistics at Syneos Health, you will play a crucial role in ensuring that the Biostatistics department meets project timelines, delivers high-quality results, adheres to project requirements and SOPs, and operates within budget constraints. Your responsibilities will include participating in the development of department SOPs, overseeing staff development and training, promoting standardized processes, and facilitating succession planning. You will be responsible for setting goals for direct reports, managing their performance, identifying training needs, supporting development plans, mentoring, and coaching staff members. By actively participating in hiring, onboarding, ...

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...

As a Statistical Modeller - Clinical, you will be responsible for utilizing your expertise in clinical trials and clinical data monitoring to develop and implement statistical models. Your role will involve working with Bayesian and Frequentist models, as well as handling EDC, CTMS, ePro, and eCOA systems. You will also be involved in RBQM, signal detection, KRI analysis, and outlier detection. In this position, a strong understanding of GCP ICH E6/8 and EMA Guidelines is essential. Proficiency in statistical software such as SAS, R, JMP Clinical, and Python will be required for data analysis and modelling. Experience with visualization tools like Tableau and Power BI will also be beneficial...

Sitero is an emerging leader in Clinical services and software solutions for the life sciences industry. We have experience and expertise in a diverse range of therapeutic areas and focus on innovative, technology-enabled solutions that allow our clients to focus on their core strengths. For early phase studies through Phase III clinical trials, our experienced team delivers high-touch services and technology to ensure the safety of all stakeholders across the clinical research community with an emphasis on ethics, compliance, and innovation. Job Title: Operations Associate II Location: Bangalore, Karnataka (Hybrid) Function: Service Delivery Site and Patient Payments ESSENTIAL DUTIES AND RE...

Let s build the future of medicine together. Join Enveda as an Research Associate / Senior Research Associate In Vitro ADME in Hyderabad, India, and help us transform natural compounds into life-changing medicines. We re a team driven by curiosity and innovation are you ready to make a difference On-Site | Hyderabad, India | Full-Time | What Makes Us Enveda Life is smart, and we can learn from it. We re reinventing drug discovery by harnessing nature s intelligence. Our platform identifies new medicines four times faster than the industry standard because patients can t wait. What sets Enveda apart isn t just what we do it s how we do it. Our culture is built on creativity, collaboration, an...

Deenanath Mangeshkar Hospital is looking for RESEARCH DOCTOR CLINICAL TRIALS to join our dynamic team and embark on a rewarding career journey Collaborate with cross-functional teams to achieve strategic outcomes Apply subject expertise to support operations, planning, and decision-making Utilize tools, analytics, or platforms relevant to the job domain Ensure compliance with policies while improving efficiency and outcomes

Primary Responsibilities: Review and analyze patient medical records for accurate code assignment Ensure adherence to coding guidelines and regulatory requirements Learn to use medical coding software Apply understanding of anatomy and physiology to interpret clinical documentation and identify applicable medical codes Stay updated on industry changes and attend relevant training sessions Ensure confidentiality and security of all patient information Comply with the terms and conditions of the employment contract, company policies and procedures, and any and all directives (such as, but not limited to, transfer and/or re-assignment to different work locations, change in teams and/or work shi...

Looking for a motivated individual to join our team as a Trainee Medical Reviewer in Bengaluru. The ideal candidate should have 0-1 years of experience. Roles and Responsibility Conduct thorough medical reviews of patient records and reports to ensure accuracy and compliance with regulatory requirements. Collaborate with cross-functional teams to identify and resolve issues related to medical review. Develop and maintain expertise in medical terminology, regulations, and guidelines. Provide high-quality support to internal stakeholders through effective communication and documentation. Stay updated with changes in regulations and guidelines affecting medical review processes. Participate in ...

Looking for a skilled Engineer - Voice Support to join our team at Omega Healthcare Management Services Pvt. Ltd., located in Navi Mumbai I. The ideal candidate will have 2-4 years of experience. Roles and Responsibility Provide technical support and resolve customer complaints via phone, email, or chat. Troubleshoot and diagnose issues with software applications and hardware systems. Collaborate with cross-functional teams to identify and implement solutions. Develop and maintain documentation of technical procedures and knowledge base articles. Analyze customer feedback and suggest improvements to processes and procedures. Participate in training and development programs to enhance skills ...

Job Tittle - R&D Clinical Trial Support Associate Location - Hyderabad About the job The Clinical Trial Support Associate (CTSA) plays a pivotal role in supporting the Clinical Operations Study Leader (COSL), Global Study Leader (GSL for EDCO) and the Clinical Operations Study Country Leader (COSCL) throughout the entire lifecycle of clinical studies. The CTSA is entrusted with managing a wide range of study, country, and site-level activities delegated by the COSL, GSL and COSCL, ensuring seamless execution and delivery of clinical trials. As the central point of oversight, the CTSA coordinates activities across all levels within a study, maintaining a comprehensive view of study progress. ...

Job Overview Provide medical expertise on pharmacovigilance services to divisions as requested The Associate Medical Safety Director participates in all aspects of Medical Safetys involvement on assigned trials and stand alone safety projects with appropriate oversight from management or more senior medical safety directors, 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 regulator...

Working with Us Challenging Meaningful Life-changing Those aren't words that are usually associated with a job But working at Bristol Myers Squibb is anything but usual Here, uniquely interesting work happens every day, in every department From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams Take your career farther than you thought possible, Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment We offer a wide varie...

Clinical/ KOL engagement - Various engagement activities including scientific discussions, RTMs, Meetings with KOLs, technical approval for new or existing brands Therapy Awareness and Adoption through conducting CNEs, workshops, nursing awareness. Required Candidate profile must be open to traveling in assigned state. Experience in Infection control / Nursing Training / Nurse educator role in Medical Disposables Organization/ Hospital in Critical Care/ Vascular Access

The main purpose of your role as an experienced professional individual contributor in Medical Affairs is to work under limited supervision and apply your subject matter knowledge effectively. Your capacity to apply skills and knowledge should meet specific needs or requirements within the field. As an experienced professional in the Medical Affairs Sub-Function, you will be responsible for overseeing the direction, planning, and execution of clinical trials and research activities. You will play a key role in data collection, implementation of clinical protocols, and ensuring completion of final reports. Additionally, you will be involved in recruiting clinical investigators, negotiating st...

As the Manager, Clinical Operations at Kenvue, you will be responsible for coordinating the operational aspects of Higher complexity clinical studies for Consumer Health products in India, APAC, or EMEA. Your role will involve collaborating with key stakeholders within the Clinical Operations global organization, local India leadership, Study directors, Clinical IT, and Bioresearch Quality & compliance (BRQC). Your primary responsibilities will include leading operational aspects of clinical studies, ensuring compliance with ICH GCP guidelines, company SOPs, and local regulations. You will serve as the point of contact for local projects funded by India R&D, participate in pipeline planning,...

As an Interventional Cardiologist at our Nangloi, Delhi location, you will be responsible for diagnosing and treating patients with heart conditions through the performance of various interventional procedures. Your expertise in interventions such as angioplasty, stenting, and atherectomy will be crucial in ensuring high-quality patient care and contributing to the success of our cardiology department. Your key responsibilities will include conducting diagnostic tests like echocardiograms and cardiac catheterizations, developing and implementing patient treatment plans, and collaborating with other specialists to offer comprehensive care. Staying updated with the latest advancements in the f...

The position of DM DNB Cardiologist is a crucial role within our healthcare organization in Narela, Delhi. As a Cardiologist, you will be responsible for providing specialized care to patients with cardiovascular issues and contributing to the overall success of our cardiology department. Your key responsibilities will include diagnosing and treating various heart conditions and diseases, performing and interpreting diagnostic tests, prescribing medications, collaborating with a multidisciplinary team, conducting rounds in hospital wards, staying updated with the latest advancements in cardiology, participating in research activities and clinical trials, providing guidance to junior medical ...

The Clinical Research Scientist position at NIRAMAI Health Analytix requires a Strong Leader, Clinical Specialist, and Medical Expert with an entrepreneurial mindset to lead the clinical research and marketing division. Your role will be crucial in furthering NIRAMAI's mission of becoming a world-class AI Healthcare organization known for its Innovation, Compliance, and Compassion. Your primary responsibilities will include developing and implementing strategies for the clinical function at NIRAMAI, coordinating international and national clinical trials, and establishing a global network of Key-Opinion-Leaders to promote the adoption of innovative diagnostic solutions. You will also be task...

As a Data Management leader, you will take charge of studies and oversee the development of project documentation, system setup, data entry, and validation procedures for junior staff. Your responsibilities will encompass all Data Management activities from study initiation to database lock, ensuring adherence to client quality standards, project timelines, and budgets. You will collaborate directly with Sponsors to understand their specific needs and lead the implementation of those requirements. Additionally, you will conduct regular reviews of client processes to ensure they align with Sponsor and Fortrea's expectations. You will lead various studies involving healthy volunteers and patie...

We are looking for a highly skilled and experienced Medical Director/Senior Consultant to lead our Oncology department at Benovymed Healthcare Private Limited. The ideal candidate will have 5-30 years of experience in the field. Roles and Responsibility Provide high-quality patient care and treatment in oncology. Lead and manage a team of healthcare professionals to achieve optimal outcomes. Develop and implement effective treatment plans for cancer patients. Collaborate with other departments to ensure comprehensive care. Stay updated with the latest medical research and advancements in oncology. Mentor and train junior staff members to enhance their skills. Job Requirements Strong knowledg...

About The Role : Job TitleRegulatory Reporting Associate LocationBangalore, India Role Description Regulatory Reporting is responsible for establishing and maintaining control frameworks designed to manage regulatory - monitoring, surveillance, compliance, transaction monitoring and screening. As a Regulatory Reporting team member, you will be responsible for managing daily reporting tasks and remediation activities. What well offer you , 100% reimbursement under childcare assistance benefit (gender neutral) Sponsorship for Industry relevant certifications and education Accident and Term life Insurance Your key responsibilities Participate in change and BAU activities. Perform daily reviews ...

Project Technical Support -III -ICMR CAR MEDTECH Project SJRI | St. Johns Research Institute Project Technical Support -III -ICMR CAR MEDTECH Project Non Division User ICMR CAR MEDTECH Project Ms. for Advance Research (CAR) on Medical Devices Development, Characterization and Validation : A clinical trials approach: Aims to provide a comprehensive platform for the end-to-end development, testing, and validation of medical devices. Project Technical Support -III No.of Vacancy:One Prefered Qualifications:Three Years Graduate degree in relevant subject/field +three years experience or PG in relevant subject/field. Experience:Minimum of 3 years Age Limit:35 years Language:English, Kannada, Telug...

As a (Manager, Clinical Operations) you will be joining the worlds largest & most comprehensive clinical research organisation, powered by healthcare intelligence, What You Will Be Doing The responsibilities of the Operations Manager include, but are not limited to: Complete ICON induction and orientation for newly employed employees, Ensure client-specific induction and orientation is planned, communicated and completed, Monitor performance and conduct annual appraisal for each employees, as applicable, Ensure timely identification and resolution of critical issues Client Relationship Managements, Agree Key Performance Indicators with client and periodically review results, You Are Bachelor...

About The Role Skill required: Pharmacovigilance Operations - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Associate Qualifications: Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 1 to 3 years About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com ...