Senior Clinical Research Associate – East Coast Based

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

📋 Description

• Conduct on-site or remote monitoring visits for Pre-Study, Initiation, Interim, and Close-Out phases.

• Ensure that investigational facilities and personnel are suitable for the execution of studies.

• Identify and assess investigators, confirming their qualifications, resources, facilities, equipment, and staff.

• Provide training to investigational site personnel as needed.

• Assist in the preparation of regulatory and/or ethics committee submissions when applicable.

• Mentor and train newly hired staff members.

• Carry out co-monitoring visits to evaluate the performance of junior staff.

⛳️ Requirements

• A College/University degree in Life Sciences or an equivalent combination of education, training, and experience.

• Significant experience in on-site monitoring for phase 2/3 clinical trials.

• Preferred experience with complex trials in oncology or rare diseases.

• Full working proficiency in English.

• Capability to plan, juggle multiple tasks, and operate effectively in a dynamic team environment.

• Strong communication, collaboration, and problem-solving abilities.

• Willingness to travel nationally.

• Proficient English language skills.

🏝️ Benefits

• A passionate and collaborative team of professionals in clinical research, pharmacovigilance, and quality consulting.

• An inclusive and diverse workplace where every voice is valued.

• Opportunities for growth and professional advancement through mentoring and training.

• A collaborative work environment that spans across countries, cultures, and time zones.

• Option for remote work.