Clinical Research Coordinator

Come join our team and make a difference as we[Y blaze the way into the future of medical discovery through world‑class clinical research.

At Pinnacle Clinical Research, we are committed to driving innovation and advancing medical knowledge. Through our rigorous research studies, we strive to unlock breakthroughs that have the potential to transform patient care and improve lives. We pride ourselves on conducting high‑quality research as a complement to the medical care that our volunteers receive from their routine care center. Together, we will
940 raise awareness about the importance of clinical research and its role in shaping the future of healthcare.

Be a part of the discovery!

PCR seeks a distrib coordinating and managing the day‑to‑day operations of assigned trials, assisting in project planning, and ensuring that pre‑established work scope, study protocol, and regulatory requirements are followed. The coordinator attends meetings to promote studies, recruits and screens participants, documents and reports on daily operations, and ensures a workflow that completes all required activities timely. The role reports directly to the Clinical Research Project Manager.

• Exercise judgement within the allowable limits of protocols, SOPs, and direction from the study investigator, Project Manager, and Director of Clinical Research Operations.
• Maintain subject and document confidentiality while complying with sponsor requirements and regulations, including FDA, GCP, ICH, HIPAA, IRB, and institutional policies.
• Complete study‑directed assessments with patients such as informed consent, subject history, adverse events, Fibroscan, test‑article handling, appointment scheduling, records review základ, treatment coordination, vital sign collection, and health assessment. catered.
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• Ensure that electronic case report forms, memos, emails, and letters related to study activities are completed and uploaded.
• Create and maintain reports and/or spreadsheets as requested.
• Enter all patient and source data timely into the Clinical Trial Management System.
• Assist with the CAPA process as needed.

Duties, responsibilities, and activities may change, or new ones may be assigned at any time.

• High school diploma or GED required.
• Bachelor’s Degree in a scientific area preferred or equivalent combination of education, training, and experience.
• Proficiency in Microsoft Office, Clinical Research IO or equivalent CTMS.
• Strong knowledge of ICH/GCP guidelines and CITI training prior to participant interaction. Re‑certification every 3 years.
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• Valid driver’s license and insurance.

• Effective communication with all internal and external contacts.
• Ability to work independently and multitask in a fast‑paced team environment.
• Strong interpersonal and confidential handling skills, positive and professional demeanor toward patients.
• Proactive problem‑solving and decision‑making, especially under pressure.
• Results‑oriented and entrepreneurial mindset.

• Work in an office/laboratory and/or clinical setting.
• Exposure to biological fluids, protective equipment required.
• Occasional domestic or international travel.
• Ability to stand or sit for 6‑10 hours, frequent mobility, occasional squatting, kneeling, or bending.
• Light to moderate lifting and carrying up to 50 lbs.

• 401(k)
• Medical, dental, vision, long‑term disability, short‑term disability, FSA, and life insurance.
3 weeks of paid time off
• 14 paid company holidays
• Scrub uniform voucher (specific positions apply)
• And more!

Pinnacle Clinical Research is an equal‑opportunity employer. All applicants will be considered for employment without regard to race, color, religion, disability, gender, national origin, age, genetic information, military or veteran status, sexual orientation, gender identity, marital status, or any other protected Federal, State/Province or local status unrelated to the performance of the work involved.