Clinical Research Site Manager
vor 2 Wochen
We are seeking a highly skilled and experienced Site Executive, GCTO to join our team at Merck Sharp & Dohme (MSD). As a key member of our clinical research team, you will be responsible for ensuring the successful execution of clinical trials at assigned sites in China.
Key Responsibilities- Develop and maintain strong relationships with site investigators and staff to ensure compliance with ICH-GCP, Sponsor SOPs, and local regulations.
- Conduct site visits, including initiation, monitoring, and close-out visits, to ensure data quality and subject safety.
- Collaborate with internal stakeholders, including CRA Manager, CRM, and TA Head, to resolve site performance and quality issues.
- Manage and maintain site documentation, including CTMS and eTMF, to ensure compliance and data integrity.
- Contribute to the development and implementation of site selection and validation strategies.
- Participate in internal meetings and workstreams as a subject matter expert on monitoring processes and systems.
- Strong understanding of ICH-GCP, Sponsor SOPs, and local regulations.
- Excellent communication and interpersonal skills.
- Ability to work independently and as part of a team.
- Strong problem-solving and analytical skills.
- Proficiency in CTMS and eTMF systems.
- Competitive salary and benefits package.
- Opportunities for professional growth and development.
- Collaborative and dynamic work environment.
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Clinical Research Site Manager
vor 2 Wochen
Schweiz Merck Sharp & Dohme (MSD) VollzeitJob SummaryMerck Sharp & Dohme (MSD) is seeking a Clinical Research Site Manager to oversee the performance and compliance of assigned protocols and sites in a country. The ideal candidate will ensure compliance with ICH/GCP and country regulations, company policies, and quality standards.Key Responsibilities:Develop and maintain strong site relationships...
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Schweiz Merck Sharp & Dohme (MSD) VollzeitJob DescriptionThe role is accountable for performance and compliance for assigned protocols and sites in a country.Under the oversight of the CRA Manager, the person ensures compliance of study conduct with ICH/GCP and country regulations, our company policies and procedures, quality standards and adverse event reporting requirements internally and...
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Schweiz Merck Sharp & Dohme (MSD) VollzeitJob Title: Clinical Research AssociateThe successful candidate will be responsible for managing and coordinating clinical research activities at assigned sites.Key Responsibilities:Develop and maintain strong relationships with site personnelEnsure compliance with ICH-GCP, sponsor SOPs, and local regulationsConduct site visits, including initiation,...
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Clinical Research Physician
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