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Clinical Trial Associate

2 months ago

Morrisville, United States Accentuate Staffing Full time

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.

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