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Clinical Research Coordinator- Manhattan, NY

The IMA Group

  • New York, New York
  • 24 days ago

    Highlights

    Our Payer Services Division meets the evaluation and screening needs of Carriers, TPAs, Public Entities and Employers and includes behavioral health and physical medicine specialty services, working with a wide range of organizations within the workers' compensation, disability, liability, and auto markets. Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple therapeutic areas through a flexible nationwide network of site locations and virtual capabilities.

    Numbers & Facts

    LocationNew York, New York
    IndustryHealthcare Services
    Company Size500 to 999 employees
    Year Founded1990
    Websitehttp://www.ima-us.com

    Description

    Description

    Job Summary:

    IMA Clinical Research is excited to welcome a Clinical Research Coordinator (CRC) with phlebotomy experience to our growing NYC team! In this role, you’ll be at the heart of medical discovery, coordinating and managing clinical trials that bring new treatments to patients who need them most. You’ll oversee studies in compliance with FDA requirements and GCP guidelines while working closely with investigators, sponsors, and clinical staff.

     

    This role requires prior experience coordinating clinical research studies involving an active investigational product (IP) supplied by an industry sponsor.

    Why join us? You’ll gain hands-on experience with innovative studies, grow your career in clinical research, and be part of a mission-driven team advancing tomorrow’s medicine. The starting salary for this position is $66,300–$75,000 annually, based on experience.

    Key Responsibilities

    • Coordinate and manage clinical trials according to sponsor protocols and SOPs.
    • Gain and maintain in-depth knowledge of study protocols and procedures.
    • Serve as a key liaison with sponsors, CROs, monitors, IRBs, labs, and clinical teams.
    • Support investigators and staff in ensuring successful study execution.
    • Ensure timely reporting of adverse and serious adverse events per protocol.
    • Maintain accurate and timely documentation in compliance with ALCOA principles.

    Qualifications & Skills

    • Minimum 2 years of clinical research and phlebotomy experience.
    • Experience coordinating clinical research studies involving an active investigational product (IP) supplied by an industry sponsor required.
    • Clinical Research Coordinator certification (CCRC) preferred.
    • Bachelor’s degree required; Master’s degree or equivalent experience preferred.
    • Skilled in managing multiple projects independently.
    • Strong communication, problem-solving, and leadership abilities.
    • Clinical healthcare experience (e.g., vitals, diagnostic tests) is a plus.

    What We Offer
    At IMA, we invest in our people and their futures:

    • Comprehensive Health Coverage: Medical, Dental, and Vision insurance.
    • Work-Life Balance: Generous PTO, holidays, and floating holiday.
    • Retirement Planning: 401k with employer match.
    • Financial & Educational Support: Tuition reimbursement and student loan repayment assistance (tax-free).
    • Family Benefits: Paid parental and maternity leave.
    • Security & Protection: Company-paid life insurance, ADD, LTD, STD, plus voluntary coverage options.

    The IMA Group is an Affirmative Action/Equal Opportunity Employer    

    Our Government Services Division supports local, state, and federal agencies and delivers professional and objective medical and psychological examinations as well as ancillary services. Our Payer Services Division meets the evaluation and screening needs of Carriers, TPAs, Public Entities and Employers and includes behavioral health and physical medicine specialty services, working with a wide range of organizations within the workers' compensation, disability, liability, and auto markets. Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple therapeutic areas through a flexible nationwide network of site locations and virtual capabilities. 

     

    #LI-BC1  #LI-ONSITE 

    About Company

    About The IMA Group

    Headquartered in Tarrytown, New York, with its main operations center in Albany, New York, The IMA Group is a national leader with a reputation for providing high-quality medical, psychological and speech and language evaluations. IMA's primary areas of focus are Social Security Disability Consultative Examinations, VA Compensation and Pension Exams, Employability Evaluations, and Occupational Health Services. Our clients include local, state, and federal agencies, as well as private insurers and corporations.

    Dr. David Pulver, IMA's President and CEO, is a Board Certified Internist with over thirty years of experience performing disability exams for Social Security Disability. Dr. Pulver has overseen IMA's growth from a single office in White Plains, NY in 1990, to its present status, with over 45 offices throughout New York, Pennsylvania, District of Columbia, Florida, Ohio, New Jersey, Connecticut, Missouri, Virginia and Vermont. Over the past 25 years, IMA has conducted more than 2.5 million evaluations and has grown to a network of more than 500 licensed providers.

    IMA Research is a multi-site research company specializing in Phase II, III and IV studies in all primary care disciplines, co-located within many of our facilities.  View IMA Research Site

    IMA provides a full range of services, including:

    Social Security Disability Consultative Examinations VA Compensation and Pension (C & P) Exams Employability Evaluations Substance Abuse Assessments and Monitoring (SAAM) Case Review Occupational Health Evaluations Police Officer/Firefighter Pre-employment Evaluations and Testing Independent Medical Examinations (IME's) (View Our IME Referral Form) Fitness for Duty Exams (FFD) DOT Physicals including Drug and BAT Testing Vocational Rehabilitation Evaluations

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