7 Clinical Research Jobs

Job Overview Manage end-to-end delivery of data management services for single/multi-service projects with minimal guidance, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Data Management (DM) team to provide high quality data management products that meet customer needs. Provide leadership to the team in the areas of project planning, execution, and close-out; Overview of financial management for data management activities; communications; and milestone deliverables. Perform role of Data Team Lead (DTL). Essential Functions Gather Study Set up requirements through discussion and communication with relevan...

Skill required: Clinical Data Services - Clinical Database Programming Designation: Clinical Data Svs Specialist Qualifications: BE Years of Experience: 7 to 11 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world¢??¢s leading biopharma companies bring their vision to life ¢??? enabling them to improve outcomes by converging around the patient, ...

Position: Transition Manager Band:C1 Shift: 11- 8 pm( Flexibile) Location: Anywhere in India(Preferred Pune or Mumbai) Work Mode: Hybrid(3 days from office and 2 Days remote) Domain: Life Science, Pharma and Medical Devices IMPORTANT NOTE:Candidate without core Business Transition experience, please do not apply for job. PRINCIPAL RESPONSIBLITIES Lead End to end active transitions, for Life Sciences, Medical Devices preferably, but other domains as well, as per business demand Manage a team of Transition managers Be the customer's SPOC for all questions, decisions, actions and updates as applicable. Support the project as the first escalation point for internal and customer issues. Drive gov...

Skill required: Clinical Data Services - Clinical Data Management Designation: Clinical Data Svs Associate Qualifications: Bachelor of Pharmacy/Master of Pharmacy/Masters in actuarial science Years of Experience: 1 to 3 years Language - Ability: English(Domestic) - Intermediate Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Songall powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 784,000 people deliver on the pro...

Role Overview: Join Amgens Mission of Serving Patients. At Amgen, you will be part of a mission to serve patients living with serious illnesses, pioneering the world of biotech since 1980. With a focus on Oncology, Inflammation, General Medicine, and Rare Disease, you will have the opportunity to impact millions of patients each year. The culture at Amgen is collaborative, innovative, and science-based, offering you the chance to thrive in a challenging environment and transform both patient lives and your career. Key Responsibilities: - Collaborate with product managers, scientists, clinicians, and commercial teams to gather, document, and analyze product requirements in the drug developmen...

We are looking for a highly skilled and experienced Senior Assistant Clinical Research to join our team at Fortis Healthcare Ltd. The ideal candidate will have a strong background in clinical research and a passion for delivering exceptional results. Roles and Responsibility Assist in the development and implementation of clinical research protocols and study designs. Coordinate with cross-functional teams, including data management, biostatistics, and medical writing. Conduct literature reviews and analyze data to inform study design and methodology decisions. Develop and maintain databases and tracking systems for clinical trial data. Collaborate with investigators and site staff to ensure...

JOB RESPONSIBILITIES Recruit and enroll study participants Input clinical research data into electronic data systems Coordinate patient visits and procedures related to research Act as a resource for study participants by answering questions and explaining related procedures Ensure the study site complies with all local and federal laws and regulations Create thorough documentation of study protocol and update it as needed Proper archival of case report forms and related documents. Coordination with all study sites. Coordination with the sponsor, ethics committee and PI for smooth conduct of study PREFERRED WORK EXPERIENCE Graduates with a Bachelor of Science or a Master of Science in areas ...