We are looking for a Clinical Research Associate to join our team!

Do you have clinical research background? Are you someone who enjoys traveling and adapts to change easily? Can you quickly connect and build strong relationships with people? Can you proactively identify a problem and develop solutions? If you have answered yes, then keep reading!

In this position you will:

  • Travel to sites conducting clinical trials to ensure all activities are in compliance with the protocol, federal regulations and ICH-GCP (Good Clinical Practice) guidelines.
  • Conduct the following monitoring visits:
    • Site Evaluation Visits
    • Site Initiation Visits
    • Routine Monitoring Visits
    • Close-out Visits
  • Oversee drug accountability, storage and disposition at investigative sites.
  • Collect and maintain investigator regulatory documents.
  • Conduct Site Endpoint Evaluation Visits when required by contract.
  • Assure proper maintenance of required records for monitoring activities and required regulatory documents per CPC requirements.

Here’s what you will need to bring to the table:

  • Nursing or bachelor’s degree (preferred but not required).
  • A basic knowledge of the Good Clinical Practice guidelines and familiarity with applicable FDA and ICH regulations for conducting clinical drug trials.
  • Minimum two years of experience as a clinical research coordinator OR experience working with clinical trial data.
  • Experience in healthcare and/or auditing as well as familiarity with medical terminology (preferred).
  • Good interpersonal communication skills, organizational skills and problem solving skills.
  • Proficiency in Microsoft Office (Word, Excel, PowerPoint).
  • Great attention to detail.
  • Ability to work as a member of a team.
  • Ability and willingness to travel up to 60%.

Note: Viable applicants will be required to demonstrate their computer skills as well as pass a background check.

Please include a short cover letter with answers to the following questions:

  1. Why would you be a good candidate for this position?
  2. How many years of relevant experience do you have?
  3. Any gaps in your employment history? Please explain.
  4. What are your salary expectations?
  5. Are you authorized to work in the United States?
  6. Do you now or will you in the future require sponsorship for employment visa status (e.g., H-1B visa status)?


About CPC:

CPC is an academically led clinical research organization that offers full service clinical trial design, oversight, and management with rapid access to Key Opinion Leaders in a variety of therapeutic areas. With over 25 years of experience, CPC has provided services to over 150 clinical trials in a variety of indications, with an emphasis on cardiovascular, wound healing, diabetes and more.

CPC has expertise in managing clinical trials from a variety of funding sources including Industry, NIH, and Investigator Initiated trials.

CPC Community Health focuses on innovative programs that reach into communities to help people find effective ways to become active, empowered and healthy. http://www.cpccommunityhealth.org/

CPC offers a comprehensive benefits package (medical, dental, vision, life, STD, LTD etc.)

An Equal Opportunity Employer

CPC provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, national origin, gender, gender identity, veteran status, marital status, sexual orientation, age, disability, genetic information or any other status protected by applicable federal, state or local law. It is our intention that all qualified applicants are given equal opportunity and that selection decisions be based on job-related factors.

Applicants with disabilities may be entitled to reasonable accommodation under the Americans with Disabilities Act (ADA) and certain state or local laws. If you need assistance, please email our Human Resources team.