Senior Research Study Manager
hace 20 horas
Merck Gruppe - Msd Sharp & Dohme seeks a Senior Clinical Research Associate with a strong background in site management and monitoring to join our team. This is a key role within the company, requiring a high level of expertise in clinical research, regulations, and compliance.
About the RoleThe successful candidate will be responsible for ensuring performance and compliance for assigned protocols and sites in their country. They will work under the oversight of the CRA manager or CRD to ensure compliance with ICH/GCP, company policies, and quality standards.
Key Responsibilities- Develops strong relationships with sites and ensures continuity of these relationships throughout all phases of the trial.
- Performs clinical study site management/monitoring activities in compliance with regulations, SOPs, and associated documents.
- Gains an in-depth understanding of the study protocol and related procedures.
- Coordinates and manages various tasks in collaboration with other sponsor roles to achieve Site Ready.
- Participates in internal meetings and workstreams as SME for monitoring processes and systems.
This role requires excellent communication skills, including the ability to understand and present technical information effectively. The ideal candidate will have a strong understanding of global, country, and regional clinical research guidelines and the ability to work within these guidelines.
RequirementsTo be successful in this role, you will need:
- Min. 4 years of direct site management (monitoring) experience in a bio/pharma/CRO.
- B.A./B.S. with a strong emphasis in science and/or biology.
We offer a competitive salary of $85,000 per year, plus benefits and opportunities for professional growth and development. If you are a motivated and experienced professional looking to take your career to the next level, we encourage you to apply.
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