Research Administration Professional
hace 5 días
Merck Gruppe - MSD Sharp & Dohme is seeking a Research Administration Professional to support the coordination and execution of clinical trials. As a key member of our operations team, this role will be responsible for supporting the administrative aspects of clinical research, including trial and site administration, document management, and meeting planning.
The responsibilities of this position include, but are not limited to:
- Trial and site administration: Ensure collation and distribution of study tools and documents, manage labeling requirements and coordinate/sign translation change requests, in collaboration with other country roles (if applicable)
- Document management: Prepare documents and correspondence, collate, distribute/ship, and archive clinical documents, e.g. eTMF, assist with eTMF reconciliation, execute eTMF Quality Control Plan, document proper destruction of clinical supplies
- Meeting planning: Organize meetings (create & track study memos/letters/protocols), support local investigator meetings (invitations, prepare materials, select venue, support vendor where applicable)
A good understanding of Global, Country/Regional Clinical Research Guidelines and ability to work within these guidelines is required. Good IT skills, particularly MS Excel, are also necessary. Effective time management, organizational and interpersonal skills, conflict management, effective communication with external customers, high sense of accountability / urgency, ability to set priorities and handle multiple tasks simultaneously in a changing environment are all required.
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Data Administration Professional
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