Clinical Trial Associate
Accentuate Staffing is partnering with a biopharmaceutical company who is hiring for a Clinical Trial Associate to join their team. This is a direct hire opportunity, offering competitive pay and benefits while working a hybrid work schedule. The ideal candidate has demonstrated experience communicating with clinical sites and drug development professionals to collect essential documents and a strong initiative to work in a fast-paced environment.
Responsibilities:
- Executes, manages and conducts studies associated with the company’s clinical development plans.
- Assists directly with project start-up, this will include the development of budgets, contracts, financials, disclosure statements and grant payments.
- Provides support for maintaining both electronic and paper document-tracking systems for all documents associated with the start-up and execution of clinical studies.
- Assists in the oversight, processing and management of all clinical project-related documents including Investigator Site Regulatory Documents, Case Report Forms (CRF) and Monitoring Reports.
- Reviews both Investigator and Project files throughout a clinical trial and follows up with CSM on any discrepancy or missing documents.
Requirements:
- Bachelor’s degree in related field combined with a minimum of 4 years of related experience.
- Clinical operations experience in phase 2 to phase 3 clinical trials including global clinical trials.
- Working knowledge of ICH GCP regulations.
- Must have extensive experience working in a sponsor environment.
- Experience in Pulmonary hypertension research.
