Feasibility Manager Precision Medicine Group

5.0 - 9.0 years

0 Lacs

karnataka

On-site

Role Overview: As a Feasibility Manager at Precision for Medicine, you will be a key member of the expert Feasibility Department team. Your role involves supporting the delivery of various projects including pre-award, post-award, rescue, and stand-alone feasibility projects. You will be responsible for conducting feasibility analysis to support business development, operational strategy teams, and site identification for both new and ongoing projects. Additionally, you may also have the opportunity to contribute to innovative projects that keep Precision for Medicine at the forefront of scientific innovation in the biotech and pharma industry. Key Responsibilities: - Support pre-award feasi...

Posted 3 weeks ago

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Senior Clinical Data Associate Precision for Medicine

5.0 - 9.0 years

0 Lacs

karnataka

On-site

As a Senior Clinical Data Associate at [Company], you will be responsible for providing data management support and assistance throughout the clinical trial data management process. Your role will involve following Standard Operating Procedures (SOPs) and regulatory directives to ensure the successful completion of assigned projects. Some key responsibilities include: - Supporting the Lead DM as a back-up and/or team member to ensure tasks are performed in a timely manner - Performing data entry for paper-CRF studies and conducting quality control of data entry - Assisting in developing CRF specifications and coordinating the review/feedback from stakeholders - Building clinical databases an...

Posted 1 month ago

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Manager - 2 Global Trial Manager SUN PHARMA

6.0 - 10.0 years

0 Lacs

gujarat

On-site

As a Global Trial Manager, Clinical Operations at Sun Pharma, you will be an integral part of the clinical development team based in Mumbai. Reporting directly to the Global Trial Leader, Clinical Operations, you will play a key role in providing global, regional, or complex local management of Sun Pharmaceuticals clinical trials. Your responsibilities will include overseeing the operational aspects of assigned projects from start to finish, ensuring adherence to protocols and regulatory requirements, and maintaining high-quality standards throughout the trial process. Your primary duties will involve managing CROs and other vendors, evaluating project progress and resources to ensure timeli...

Posted 4 months ago

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