Description
Allucent is hiring a Start-Up Associate (Contractor) to coordinate and support clinical trial site start-up activities from essential document collection and IEC/IRB submissions through site initiation and handover to the CRA. The role involves tracking milestones in CTMS, maintaining the eTMF, adapting informed consent forms, resolving document discrepancies, and potentially supporting feasibility, site identification, and clinical trial agreement and budget negotiations. Candidates need a bachelor's degree in life sciences, healthcare, or a related biological discipline or equivalent experience, at least 3 years in drug development or clinical research, at least 2 years in a similar CRO/pharma role, regulatory knowledge, strong communication and organizational skills, attention to detail, and proficiency with Microsoft Office.
