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About the role

We are a team of clinical trial experts dedicated to the success of our clients, ensuring patients receive much-needed treatments. Our culture prioritizes patients, quality, employee growth, and community involvement. This role is for someone passionate about clinical trials, ready to lead and manage studies.

Responsibilities

• Lead and manage clinical teams on study timelines and project scope, ensuring quality delivery.
• Ensure appropriate communication and ongoing oversight of assigned trials.
• Participate in and present at sponsor meetings.
• Mentor and train team members.
• Identify and address challenges to study timelines and deliverables.
• Contribute to company and department initiatives to improve processes and procedures.

Requirements

• Minimum 5 years of clinical research experience or proven competencies with significant clinical monitoring experience.
• Preferred 2 years of CTM experience at a CRO, Pharma, or Biotech company.
• Moderate independent field monitoring experience.
• Senior Clinical Trial Lead/Manager: Minimum 7 years of clinical research experience or proven competencies with significant clinical monitoring experience.
• Preferred 4 years of CTM experience at a CRO, Pharma, or Biotech company.
• Experience with Microsoft Office Products (Outlook, Word, Excel, PowerPoint).
• Experience with various EDC and eTMF systems.
• Excellent communication and interpersonal skills.
• Excellent organizational skills, attention to detail, and a customer service demeanor.
• Availability for domestic and international travel, including overnight stays.

Qualifications

• Bachelor's degree or equivalent in a science or health-related field.
• Passion for bringing lifesaving and life-altering treatments to market.
• Loves having responsibility and a say in how clinical trials are run.
• Planned ahead but adaptable to last-minute changes.
• Handles study timelines with ease and maintains quality.
• Communicates clearly and concisely.
• Identifies and addresses risks proactively.
• Thrives with minimal direction.
• Works well in a team environment.

Skills

• Demonstrated computer skills (MS Office, PowerPoint, etc.).
• Software experience (CTMS, eTMF, EDC, IXRS, RTSM, etc.).
• Develops positive working relationships with internal and external organizations.
• Excellent time management, negotiation, critical thinking, decision-making, analytical, and interpersonal skills.
• Results-oriented, accountable, motivated, and flexible.
• In-depth proven experience in pharmaceutical and/or device research.

Benefits

Not specified.

Pay

Not specified.

Schedule

Not specified.

Company

Equal Opportunity Employer. Precision Medicine Group does not discriminate on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.