Clinical Trial Manager

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

📋 Description

• Lead the local clinical trial team in the U.S. and supervise daily clinical trial operations.

• Oversee trial preparation, execution, monitoring coordination, and closeout processes.

• Ensure that clinical trials achieve recruitment goals, adhere to project timelines, stay within budget, and meet quality benchmarks.

• Maintain adherence to GCP guidelines, clinical research regulations, and internal quality standards.

• Collaborate with Clinical Research Associates (CRAs), investigators, site personnel, and Site Monitoring Leads.

• Act as the main point of contact for CRAs, investigators, and clinical research sites.

• Work alongside global, regional, and cross-functional teams to guarantee successful trial execution.

• Track trial progress, recognize potential risks, and apply appropriate risk mitigation strategies.

• Ensure the safety of patients, the integrity of clinical trials, and the accuracy of trial data.

• Represent the organization in internal and external meetings, including engagements with investigational sites and regulatory bodies.

• Handle multiple clinical trial assignments while managing competing priorities.

• Contribute to innovative clinical trial management initiatives and process enhancements.

⛳️ Requirements

• A Bachelor's degree with at least 6 years of clinical research experience; OR a Master's degree or PharmD with a minimum of 4 years of clinical research experience; OR a PhD or MD with at least 2 years of clinical research experience.

• Experience in managing pediatric clinical trials is essential.

• Background in the pharmaceutical industry is preferred.

• Strong knowledge of clinical trial operations, clinical development processes, and regulatory standards.

• Familiarity with Good Clinical Practice (GCP) and compliance standards in clinical research.

• Proven experience in clinical trial project management and team leadership.

• Excellent stakeholder management and cross-functional collaboration abilities.

• Capability to manage complex clinical studies across multiple sites, countries, suppliers, and participants.

• Exceptional communication, organizational, and problem-solving skills.

• Ability to balance competing priorities, resolve conflicts, and influence stakeholders effectively.

• Strong skills in risk assessment, planning, and coordination.

• Willingness to travel domestically approximately 10–20% of the time.

• This position is primarily remote within the United States.

🏝️ Benefits

• Paid weekly.

• Client holidays are compensated.

• Sick time is provided in accordance with applicable local laws.