Clinical Research Coordinator

Clinical Research Coordinator I

Join as a Clinical Research Coordinator I at Cen Exel.

Cen Exel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence are renowned for their expertise in complex early‑phase trials and in‑patient capability across specialties such as Psychiatry, Acute Post‑Op Pain, Asian Bridging, Dermatology, GI, and Neurology. We prioritize quality, teamwork, and experienced clinical research managers.

Responsible for coordinating clinical trials with strict adherence to ICH, GCP, protocol, company guidelines, regulations, and policies.

$28-33/h depending on experience, education and skillset.

After 30 days of employment, employees receive a generous benefits package that includes health insurance, dental, vision, life insurance, long‑term disability, short‑term disability, and participation in a 401(k) plan.

• Assists with coordinating all aspects of patient involvement from study initiation until study completion.
• Organizes research information for clinical trials.
• Observes subjects and assists with data analysis and reporting.
• Schedules the collection of data.
• Documents adverse events, protocol deviations, and other unanticipated problems appropriately.
• Reports research data to maintain quality and compliance.
• Performs administrative and regulatory duties related to the study as appropriate.
• Participates in other protocol development activities.
• Ensures site receives accurate information and supplies from sponsors (i.e.: source, protocol, scales, supplies, approvals, contacts, etc.).
• Educates potential participants and caregivers on protocol‑specific details and expectations.
• Performs safety and efficacy assessments per protocol (vital signs, EKGs, blood draws and other assessments as assigned).
• Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

• High school graduate or equivalent;
  Bachelor’s Degree preferred.
• 0‑3 years of experience in the medical field.
• Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials.
• Strong leadership and mentorship skills.
• Developing and maintaining effective working relationships at all levels of the organization, along with those at the sponsor and vendor level.
• Crisis management and problem‑solving skills; ability to react calmly and effectively in emergent situations.
• Works independently as well as functioning as part of a team.
• Must be able to effectively communicate verbally and in writing.

• Indoor, office environment.
• Shift work, depending on location.
• Essential physical requirements include sitting, typing, standing, and walking.
• Lightly active position, occasional lifting of up to 20 pounds. Rarely lift over 20 pounds.
• Reporting to work, as scheduled, is essential.
• Overnight travel may be required for training and/or investigative meetings.

Cen Exel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability.