Title: Clinical Research Coordinator
Location: Manchester, NH 
Type/Duration: Contract, 6 month/renewable, 100% onsite
Schedule: Monday-Friday, core daytime business hours based on clinic hours, could have some earlier morning starts
Start Date: ASAP

Joule is currently looking to hire a Clinical Research Coordinator to work onsite in Manchester, NH. You must have at least 1 year of experience working as a CRC within drug trials.

Summary of Key Responsibilities

Primary responsibility is to screen, enroll, and follow study subjects ensuring protocol compliance and monitoring while the subjects are on study. Responsible for all data collection, source documentation, completing study-specific case report forms, and submission of adverse experience reports.

Duties and Responsibilities

Duties include but are not limited to:

Supports enrolling patients onto the clinical trial through screening, enrollment and follow up of eligible subjects according to protocol requirements

Ensures the protection of study patients by verifying informed consent procedures and adheres to protocol requirements/compliance

Collects, completes, and enters data into study-specific case report forms or electronic data capture systems

Ensures timely and accurate data completion

Collects blood samples and tracks shipments and requests supplies as needed

Implements study-specific communications

Ensures timely adherence to protocol requirements

Responsible for completion of all required documentation

Maintains accurate and complete records including regulatory documents when applicable, signed informed consent forms, source documentation, subject logs and study-related communications

Communicates all study-related issues to appropriate study colleagues or manager

Apprises principal investigator and management of all study-specific medical issues for guidance

Attends study-specific meetings as required or asked to do so

Reviews and responds to any monitoring findings and escalates issues

Requirements

Bachelor's degree required, Master’s degree preferred

CCRC preferred

1+ years of relevant clinical trials experience, 5+ years preferred

Must have clinical research/trials experience (CRC experience needed)

Fundamental understanding of medical and research operations terminology (nice to have)

Recognize circumstances requiring prompt escalation to PI, IRB, or Supervisor (nice to have)

Ref: #568-Clinical

System One, and its subsidiaries including Joulé, ALTA IT Services, TeamPeople, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.