Senior Clinical Research Associate

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

📋 Description

• Conduct Pre-Study, Initiation, Interim, and Close-Out monitoring visits either on-site or remotely.

• Ensure that the facilities and staff at investigational sites are suitable for the conduct of the study.

• Identify and assess investigators, confirming their qualifications, resources, facilities, equipment, and staff throughout the duration of the study.

• Provide training to investigational site personnel as necessary.

• Assist in the preparation of regulatory and/or Ethics Committee submissions when applicable.

• Mentor and guide new staff members.

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

⛳️ Requirements

• A college or university degree in Life Sciences or an equivalent combination of education, training, and experience.

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

• Ideally possess experience with complex trials in oncology or rare diseases.

• Full working proficiency in English.

• Capability to plan, multitask, and thrive in a dynamic team environment.

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

• Willingness to travel nationally.

🏝️ Benefits

• Option for remote work.

• Engaging and collaborative team environment.

• Opportunity to contribute to the development of safe and effective pharmaceutical treatments for patients.

• Mentoring and training opportunities available.

• A diverse and inclusive workplace.

• Opportunities to make a meaningful impact on patients' lives.