Sr. Clinical Research Coordinator
Company: Nesco Resource
Location: Manchester
Posted on: July 1, 2025
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Job Description:
Position Summary The Senior Clinical Research Coordinator is
responsible for overseeing the coordination of multiple research
protocols while acting as a liaison for investigators, research
personnel, and site staff. This role plays a key part in ensuring
research compliance, patient safety, and the smooth execution of
study protocols. Major Responsibilities Research Operations Perform
day-to-day operational tasks for multiple research protocols. Serve
as a primary contact between site research teams, sponsors, and
leadership. Collaborate with various internal departments including
finance, administration, and the Institutional Review Board (IRB)
as applicable. Coordinate assessments and submissions from initial
feasibility through study closeout. Ensure protocol awareness among
site personnel including physicians, nurses, clinical staff, and
administrative staff. Accurately complete and document
protocol-required assessments (e.g., medication forms,
questionnaires, vital signs, laboratory timing). Perform
calculations and documentation for clinical scores such as BSA,
mRS, NIHSS, and STS risk scores as required. Document all patient
and study-related interactions, including adverse events, follow-up
visits, interventions, and communications. Ensure appointments,
imaging, and procedures are scheduled per protocol guidelines.
Address data queries and submit requested documentation in
accordance with SOPs. Facilitate the re-consent process for
patients as necessary. Support the research team in identifying and
mitigating compliance risks. Site Development Partner with
investigators and site staff to assess feasibility and optimize
performance. Meet regularly with physicians and administrators to
review study progress and address concerns. Collaborate with
cross-functional departments to implement research-related
processes. Present study updates during site meetings (section
meetings, service line reviews, etc.). Guide the research team on
managing non-compliance in data or study activities. Reporting &
Analysis Monitor patient enrollment trends through weekly reporting
and communicate status updates to leadership. Support continuing
education and training initiatives for investigators and site
teams. Education & Experience Bachelor's Degree Required Master's
Degree Preferred 1 years of relevant experience Required 5 years of
relevant experience Preferred Or an equivalent combination of
education and/or experience. Licenses, Certifications & Training
Certified Clinical Research Coordinator (ACRP or CCRP) Preferred
Knowledge, Skills, and Abilities Knowledge Understanding of
organizational policies, SOPs, and research systems. Knowledge of
ICH guidelines and the Code of Federal Regulations (CFR) as applied
to clinical research. Familiarity with medical and research
terminology. Ability to identify and escalate issues to the
Principal Investigator (PI), IRB, or supervisor when appropriate.
Skills Strong communication and interpersonal abilities. Excellent
organizational and time management skills. Basic clinical trial
competencies including ECG acquisition, phlebotomy, and specimen
handling. Ability to effectively interface with diverse internal
and external stakeholders. Abilities High attention to detail.
Self-motivated and proactive. Strong problem-solving and critical
thinking skills. Clinical Competencies This position may require
proficiency in clinical tasks such as: Electrocardiogram (ECG)
acquisition. Phlebotomy. Specimen processing, handling, storage,
and shipping. Travel Requirements Occasional Travel: May be
required on an as-needed basis, but not regularly. Benefits Nesco
Resource offers a comprehensive benefits package including:
Medical, Vision, and Dental coverage through a Minimum Essential
Coverage (MEC) plan. 401(k) retirement plan. Employee Assistance
Program (EAP). Equal Employment Opportunity Statement Nesco
Resource is committed to providing equal employment opportunities
to all employees and applicants. We prohibit discrimination and
harassment of any kind, regardless of race, color, religion, age,
sex, national origin, disability status, genetics, protected
veteran status, sexual orientation, gender identity or expression,
or any other characteristic protected by law.
Keywords: Nesco Resource, Brookline , Sr. Clinical Research Coordinator, Healthcare , Manchester, Massachusetts
