Job Title : Clinical Trials Specialist
Job Description
The Clinical Trials Specialist supports Clinical Study Leads in the overall execution of global clinical trials, including both internally sourced studies and those outsourced to CROs.
Responsibilities include scheduling and coordinating meetings, preparing agendas, presentation materials, and minutes for clinical study team meetings.
The role involves collating data for feasibility assessments and site selection, reviewing site usability databases, and contributing to the review of study documents such as informed consent forms and case report forms.
The Specialist will compile and maintain study manuals, manage the eTMF, track site activation, enrollment, and monitoring visits, and escalate any issues or delays.
Additional duties include monitoring investigator / site status, supporting clinical trial registry postings, contributing to Blind Data Review Meetings, managing Third Party Vendors, and participating in SOP revisions or departmental initiatives.
Soft Skills
- Strong organizational skills
- Attention to detail
- Effective communication skills
- Ability to manage multiple tasks
Clinical Trials Specialist
The Clinical Trials Specialist supports Clinical Study Leads in the overall execution of global clinical trials, including both internally sourced studies and those outsourced to CROs. Job Title: Clinical Trials Specialist. Responsibilities include scheduling and coordinating meetings, preparing age...
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