• Clinical Research Coordinator

    Actalent (Evesham, NJ)


    Clinical Research Coordinator

     

    Direct Hire Opportunity

    Job Description

    The Clinical Research Coordinator will be responsible for coordinating all aspects of clinical trials with the strictest adherence to ICH, GCP, protocol, and company guidelines, regulations, and policies.

    Essential Responsibilities and Duties:

    + Coordinates all aspects of patient involvement from study initiation until study completion.

    + Study start-up activities: Assists in the creation of thorough and accurate source documents.

    + Study start-up activities: Works collaboratively with internal departments, sponsors and investigators to ensure protocols are understood and assists in training staff members.

    + Study start-up activities: Participates in IMs (Inclusion Management) and SIVs (Site Initiation Visits); communicating with sponsors and representatives.

    + Study start-up activities: Ensures site receives accurate information and supplies from sponsors (i.e.: source, protocol, scales, supplies, approvals, contacts, etc.).

    + Screening and enrolling activities: Assists in reviewing all participant history from Pre-Enrollment and Enrollment departments confirming information with potential participant and study physician.

    + Screening and enrolling activities: Educates potential participants and caregivers on protocol specific details and expectations.

    + Screening and enrolling activities: Works with the physician to address all questions and concerns related to the trial and informed consent process.

    + Screening and enrolling activities: Maintains thorough knowledge of study specific inclusion/exclusion criteria.

    + Coordinates scheduled visits, adhering to protocol visit windows and timelines.

    + Performs safety and efficacy assessments per protocol (vital signs, EKGs, blood draws and other assessments as assigned).

    + Collaborates with the research pharmacist to perform drug accountability and compliance at each visit and educating subject on proper dosing regimen.

     

    Required Skills & Qualifications

     

    + Must be bilingual in English and Spanish.

    + Must have at least 2 years of clinical research coordinator experience, preferably in interventional drug studies.

    + Experience with high enrolling studies highly preferred.

    Pay and Benefits

    The pay range for this position is $47840.00 - $72800.00/yr.

     

    Benefits package available.Client observes 7 holidays annually including: New Years Day, Memorial Day, Independence Day, Labor Day, Thanksgiving, the day after Thanksgiving, & Christmas.

     

    Workplace Type

     

    This is a fully onsite position in Evesham,NJ.

     

    Application Deadline

     

    This position is anticipated to close on Oct 31, 2025.

    About Actalent

    Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

     

    The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

     

    If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.