Senior Clinical Research Coordinator
Company: Innovo Research
Location: Wilmington
Posted on: April 4, 2026
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Job Description:
Description JOB SUMMARY The Senior CRC will work closely with
Principal Investigators and clinical research teams to coordinate
the daily operations of clinical research studies and o versee
clinical research staff performing clinical functions at the
designated Innovo Research partner site The Senior CRC will be
responsible for making sure that all clinical research activities
are efficiently executed, and conducted in a professional manner
that is compliant with all human research subject regulations.
RESPONSIBILITIES Assist with mentoring and training clinical
research staff. Perform clinical functions i.e. phlebotomy,
monitoring vital signs on study participants, etc., when warranted;
educate family and contribute to the care and evaluation of
subjects, including determining preliminary inclusion/ exclusion
criteria. Liaises with agencies, pharmaceutical companies,
laboratories, vendors, equipment, and supply companies as needed;
oversees availability of supplies and/or equipment for studies .
Manage multiple concurrent trials - screening, recruiting, and
enrollment, perform patient/research participant scheduling,
coordinate protocol-related research procedures, study visits, and
follow—up, collect patient/ research participant history, collect
and maintain source documentation, perform data entry and query
resolution, prepare IRB submissions, update required modifications,
continuing reviews, and reportable events. Develop strong working
relationships and maintain effective communication with study team
members. Completes all protocol-related training and adheres to IRB
approved protocol(s) Support the collection and review of required
essential study documents and reports. Order supportive study
supplies (e.g., contracts, IXRS, lab kits, non-clinical supply
materials, imaging, and laboratory handling manuals, etc.). Assist
in the informed consent process of research subjects. Support and
advocate for the safety of research subjects. Facilitate pre-study,
site qualification, study initiation, monitoring visits, and study
close-out activities. Collect, process, and ship laboratory
specimens. Comply with Innovo, Clinic, and Sponsor policies,
standard operating procedures (SOPs), applicable regulatory
requirements and guidelines. Performs all additional duties as
assigned. Qualifications Qualifications At least 3-5 years of
experience coordinating clinical trials, including the activities
listed above. Prior cardiology experience not required, but would
be a great to have. BS/BA in Life Science or related discipline.
Certified Clinical Research Coordinator (CCRC) certification
preferred. Previous GCP training and certification required and
working knowledge of current ICH GCP guidelines and applicable
regulations. Experience in a clinical setting. Demonstrated ability
in positive relationship building. Previous experience with
training and mentoring other clinical research professionals is a
plus. Strong interpersonal skills with attention to detail a must.
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 required.
Ability to work independently, prioritize, and work with a matrix
team environment is essential. Ability to travel for Clinic
activities, and attend investigator meetings or vendor
visits/audits, as required. BENEFITS (full-time) Competitive salary
Health Insurance Dental Insurance Disability Insurance Life
Insurance Paid Time Off Vision Insurance WORKING CONDITIONS This
job operates in a professional and clinical environment with
occasional visits to other Innovo Research partner sites/clinics.
This role routinely uses standard office equipment such as
computers, phones, and scanners. There is frequent exposure to
communicable diseases, toxic substances, ionizing radiation,
medicinal preparations, and other conditions common to a clinic
environment. Varied activities include standing, walking, reaching,
bending, and lifting. 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. This is an exempt position under the federal and
state wage and hour laws, which means you are not eligible for
overtime pay beyond your salary. Employees are expected to work 40
hours a week. Occasional evening and weekend work may be required
as job duties demand. The above statements are intended to describe
the general nature and level of work being performed by individuals
assigned to this position. They are not intended to be construed as
an exhaustive list of responsibilities, duties, and skills required
of personnel. More in-depth information can be found in SOP's,
working guidelines, policies, etc. Innovo Research is committed to
the principle of equal employment opportunity for all employees and
to providing employees with a work environment free of
discrimination and harassment. All employment decisions at Innovo
are based on business needs, job requirements and individual
qualifications, without regard to race, color, religion or belief,
national, social or ethnic origin, sex (including pregnancy), age,
physical, mental or sensory disability, HIV Status, sexual
orientation, gender identity and/or expression, marital, civil
union or domestic partnership status, past or present military
service, family medical history or genetic information, family or
parental status, or any other status protected by the laws or
regulations in the locations where we operate. Innovo Research will
not tolerate discrimination or harassment based on any of these
characteristics. In addition, Innovo will provide reasonable
accommodations for qualified individuals with disabilities.
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.
Keywords: Innovo Research, Fayetteville , Senior Clinical Research Coordinator, Science, Research & Development , Wilmington, North Carolina
