Clinical Research Coordinator

Wake Research

Clinical Research Coordinator

Piscataway, NJ +3 locations
Full Time
Paid
  • Responsibilities

    Job Description

    The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the guidance of the clinical research site management and Principal Investigator (PI). While the PI is primarily responsible for the overall conduct of the clinical trial, the CRC manages, supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.

    Essential Duties and Responsibilities:

    • Assisting trial Investigator in screening and review of potential study participants eligibility
    • Maintaining case report forms, charts and documentation
    • Mentoring, training, and high-level oversight of other clinical research coordinators and research assistants
    • Ensuring that all clinical activities are carried out in accordance with established research protocol and standards in compliance with all applicable laws, regulations, policies, and procedural requirements
    • Collecting and entering data as necessary
    • Assist management with potential new hire selection and shadowing process
    • Assist with study start-up, maintenance, and close-out of studies as needed for those on the team
    • Ability to be flexible with study assignments
  • Qualifications

    Qualifications

    • Clinical Research Coordinator with 1-2 years of experience
    • Phlebotomy experience required and appropriate certification/licensure in the state of CA is highly preferred
    • Excellent verbal & written communication skills
    • Ability to learn quickly, read and understand complex protocols, follow very detailed directions, and multi-tasking
    • Must be able to maintain strict confidentiality of patients, employees, and company information at all times and adhere to HIPAA Guidelines
    • Extensive clinical trial knowledge through education and/or experience
    • Successful completion of GCP Certification and Advanced CRC preferred
    • Detail-oriented
    • Familiarity with the Code of Federal Regulations as they pertain to human subject protection
    • Strong interpersonal skills

    Additional Information

    About M3:

    M3 USA is at the forefront of healthcare innovation, offering digital solutions across healthcare, life sciences, pharmaceuticals, and more. Since our inception in 2000, we’ve seen remarkable growth, fueled by our mission to utilize the internet for a healthier world and more efficient healthcare systems.

    Our success is anchored in our trusted digital platforms that engage physician communities globally, facilitating impactful medical education, precise job placement, and insightful market research. M3 USA prides itself on a dynamic and innovative work environment where every team member contributes to global health advancements.

    Joining M3 USA means being part of a dedicated team striving to make a significant difference in healthcare. We provide a unique opportunity for you to be at the cutting edge of healthcare innovation, shaping the future in a meaningful career. Embrace the chance to drive change with M3 USA.

    Benefits:

    A career opportunity with M3 Wake Research offers competitive wages, and benefits such as:

    • 401(k), 401(k) matching
    • Dental insurance
    • Disability insurance
    • Employee assistance program
    • Flexible spending account
    • Health insurance
    • Life insurance
    • Paid time off
    • Vision insurance

    *This position provides compensation of $20/hr - $38/hr.

    *M3 reserves the right to change this job description to meet the business needs of the organization

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  • Industry
    Biotechnology
  • Locations
    Tucson, AZ • San Diego, CA • Piscataway, NJ • charleston, SC