Senior Documentation Specialist
Alentis Therapeutics
· Allschwil
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·
Accepting first candidate pitches
Standard Working Hours
Full-time schedule
Competitive
Offered by host company
Certificate & LOR
Official recommendation
3 Months
Live until 2027-01
Job Description & Overview
About this position As the Senior Documentation Specialist, you ensure the effective management, quality, completeness, and inspection readiness of essential clinical trial documentation for assigned studies, programmes or documentation activities, including the sponsor TMF and oversight of CRO and laboratory TMFs. You acts as an experienced TMF specialist, working closely with Clinical Operations and cross-functional study teams to provide expert guidance on document processes, compliance, risk
Key Responsibilities
- functional study teams to provide expert guidance on document processes, compliance, risk
Stipend & Incentive Qualification Criteria
Stipend is paid upon completing assigned project milestones along with maintaining required attendance and task completion as evaluated by the host organisation.
Skills & Tech Stack
Full Stack Development
Problem Solving
Communication
Analytical Skills
Apply by: 2027-01-23
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Stipend, if applicable, is contingent on assignment to a paid project and completion of required certifications. Full terms apply.