Senior Clinical Research Coordinator
$51,227–$70,437 year
On-siteWilmington, North Carolina, United States
Job Summary
Coordinate daily operations of clinical research studies at the designated Innovo Research partner site, including screening, recruiting, enrollment, and managing multiple concurrent trials. Perform clinical functions such as phlebotomy, vital signs monitoring, and specimen collection while assisting with informed consent processes. Liaise with agencies, pharmaceutical companies, and vendors to oversee supply and equipment availability, and facilitate pre-study, site qualification, monitoring visits, and study close-out activities. Support the collection and review of essential study documents, prepare IRB submissions, and resolve data queries. Mentor and train clinical research staff, ensuring all activities comply with human research subject regulations and ICH GCP guidelines.
Required Qualifications
- At least 3-5 years of experience coordinating clinical trials
- BS/BA in Life Science or related discipline
- Previous GCP training and certification
- Working knowledge of current ICH GCP guidelines and applicable regulations
- Experience in a clinical setting
- Strong interpersonal skills with attention to detail
- Positive attitude and ability to interact with all levels of staff to coordinate and execute study activities
- Demonstrated proficiency with word processing, spreadsheet, database, and presentation software (MS Office skills such as Outlook, Word, Excel, PowerPoint, SharePoint) and with clinical trial master filing systems
- Strong organization/prioritization skills for the management of multiple concurrent projects
- An understanding of Regulatory and Central/Local ethic submission processes
- Ability to manage multiple competing priorities within various clinical trials
- Excellent verbal and written communication skills
- Ability to work independently, prioritize, and work with a matrix team environment
- Ability to travel for Clinic activities, and attend investigator meetings or vendor visits/audits, as required
- Requires full range of body motion including handling and lifting patients, manual and finger dexterity, and eye-hand coordination
- Requires standing and walking for extensive periods of time
- Occasionally lifts and carries items weighing up to 50 pounds
- Requires corrected vision and hearing to normal range
- Due to the nature of this position, employees are expected to work in person
- Employees are expected to work 40 hours a week
- Occasional evening and weekend work may be required as job duties demand
- Applicants must be authorized to work for ANY employer in the U.S.
- We are unable to sponsor or take over sponsorship of an employment Visa at this time
Desired Qualifications
- Experience in cardiology
- Certified Clinical Research Coordinator (CCRC) certification
- Previous experience with training and mentoring other clinical research professionals
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