Clinical Trials Manager

This is a fully remote position, open to applicants in United States.

📋 Description

• Overseeing and coordinating all facets of a clinical study.

• Monitor clinical trial sites while supporting the Clinical Program Manager in managing the study.

• Prepare and assess pertinent documents such as protocols, informed consents, and clinical study reports.

• Assist in the formulation of the study budget and engage in the selection of CROs/vendors.

• Ensure the effectiveness of the site budget/contract process and educate stakeholders on study requirements.

• Potentially create scientific communications within the organization.

• Travel is a requirement.

⛳️ Requirements

• A minimum of 6 years of experience in managing clinical trials.

• A BS or BA in a relevant scientific field or an RN (2 or 3-year certificate).

• In-depth knowledge and comprehension of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs relevant to clinical trials.

• Competence in managing CROs/vendors and adhering to study timelines.

• Strong teamwork, communication, decision-making, and organizational abilities.

• Capable of prioritizing multiple tasks and serving as a resource for others in the organization.

🏝️ Benefits

• Company-sponsored medical, dental, vision, and life insurance plans*

• Discretionary annual bonus

• Discretionary stock-based long-term incentives (eligibility may vary based on role)

• Paid time off