Clinical Operations Manager
Pinnacle Clinical Research
San Antonio, Texas
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JOB DETAILS
LOCATION
San Antonio, Texas
POSTED
7 days ago
Come join our team and make a difference as we 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 raise awareness about the importance of clinical research and its role in shaping the future of healthcare.
Summary: The Clinical Operations Manager is responsible for operational implementation of assigned studies at their research site. The incumbent supervises clinical trial staff and works closely with the Principal Investigator, Site Director and Regional Director, and cross-functional teams to ensure successful completion of research activities. This role serves as the primary liaison between the research site, sponsors, CROs, and other stakeholders while maintaining compliance with regulations.
Duties and Responsibilities:
Clinical Trial Management:
- Oversee daily operations of clinical research staff and studies.
- Coordinate multiple projects with competing priorities and deadlines.
- Monitor adherence to protocols and study timelines.
- Act as primary liaison with sponsors, CROs, and vendors.
- Prepare for and facilitate study monitor visits.
Regulatory Compliance:
- Ensure adherence to Standard Operating Procedures (SOPs), FDA regulations, and other regulatory references.
- Maintain subject and document confidentiality and privacy.
- Assist with regulatory submissions and file maintenance.
- Create and implement corrective and preventive action plans when appropriate.
Study Documentation:
- Supervise creation and completion of study-related documents.
- Supervise completion of case report forms.
- Supervise documentation of adverse events and subject history.
- Prepare reports as requested.
Study Participant Coordination:
- Supervise study assessments with study participants including informed consent.
- Supervise subject screening and recruitment.
- Supervise appointment scheduling and visit implementation.
- Supervise collection of vital signs and study participant assessments.
- Supervise phlebotomy, specimen processing, and biological sample shipping.
Resource Management:
- Identify departmental needs for supplies, staffing, and equipment.
- Improve research processes within established guidelines.
Supervisory Responsibilities: Directly supervises Clinical Research Coordinators and Research Assistants, ensuring compliance with SOPs and regulations. Carries out supervisory responsibilities according to organizational policies and applicable laws, including:
- Training employees.
- Planning, assigning, and directing work (with management guidance).
- Appraising performance.
- Addressing complaints and resolving problems.
Education/Experience:
- High school diploma or GED required; Bachelor's degree preferred.
- Three to five years of experience in a Clinical Research Coordinator role.
- Previous experience managing clinical research coordinators preferred.
- For CNS sites, experience conducting rating scales such as MMSE.
Certificates and Licenses:
- Good Clinical Practice training certification.
- IATA training certification.
- Valid driver's license and insurance.
Knowledge, Skills, and Other Abilities:
- Strong oral and written communication abilities.
- Excellent organizational skills and attention to detail.
- Professional interpersonal skills with a positive demeanor.
- Adaptability to changing priorities.
- Medical knowledge including terminology.
- Thorough understanding of regulations, regulatory guidance, and SOPs.
- Proficiency with Microsoft Office, web browsers, and electronic case report form systems.
Work Environment and Physical demands:
The work environment and physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
- Office/laboratory and clinical environment.
- Exposure to biological fluids and/or bloodborne pathogens.
- Personal protective equipment required.
- Occasional domestic and international travel.
- Ability to maintain upright/stationary position for 6-10 hours daily.
- Frequent mobility required.
- Occasional squatting, kneeling, or bending.
- Light to moderate lifting (20-50 lbs).
Perks of working at Pinnacle Clinical Research:
- 401k.
- Medical, dental, vision, long term disability, short term disability, FSA, and life insurance.
- 3 weeks of paid time off.
- 14 paid company holidays.
- Scrub voucher (for eligible positions).
- 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.
About Pinnacle Clinical Research:
Pinnacle Clinical Research Network provides world-class clinical trial solutions to its member sites, sponsors, CROs, researchers and patients to accelerate the results of their trials. By advocating for quality, integrity and diversity in clinical research data, Pinnacle is dedicated to advancing unmet areas of medical research and leading pivotal scientific discoveries.
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