We are looking for a Project Manager to join our team!

Are you someone who can provide excellent leadership to not only project teams, but also to clients? Are you well organized, but adaptable to unexpected changes? Someone who is able to see the bigger picture, without losing sight of the day-to-day tasks? If the answer is yes, keep reading!

This role is ideal for an individual who can motivate teams to do great work collaboratively in order to produce the best quality outcomes possible.

 In this position you will:

  • Serve as the primary point of contact for industry sponsored clinical trials.
  • Manage multidisciplinary project team members.
  • Monitor project scope, timelines and deliverables from project initiation to close out.
  • Ensure the overall quality of project services and deliverables.
  • Participate in the design, writing and/or review of all project-related essential documents including protocols, project management plans, case report forms, statistical analysis plans, Project Management Plans, ICF templates, Study Procedure Manuals, source documents, site newsletters, study reports and monitoring plans and report templates.
  • Adhere to local, federal and international regulations, guidelines and CPC Policies, Standard Operating Procedures (SOPs) and Work Instructions (WIs).

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

  • A minimum of a BA/BS in a scientific field (or equivalent knowledge/experience)
  • A minimum of 4 years of experience in a clinical research setting (required), including a minimum of 2 years of project management experience in clinical research.
  • Thorough knowledge of the Good Clinical Practice guidelines and applicable FDA and ICH regulations for conducting clinical drug trials.
  • Experience with MS Office including Outlook, Word and Excel.
  • Excellent interpersonal communication skills and a great attention to detail.
  • Ability to manage conflicts and resolve problems effectively.
  • Ability and willingness to travel up to 25%.

Note: Viable applicants will be required to pass a background check.

At this time CPC is not able to provide relocation assistance to out-of-state candidates.

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

  • Why would you be a good candidate for this position?
  • How many years of relevant experience do you have?
  • Any gaps in your employment history? Please explain.
  • What are your salary expectations?
  • Are you authorized to work in the United States?
  • 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’s proprietary database contains more than 1000 clinical investigators located throughout the world.

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.)