cpc

Clinical & Endpoint Research Associate

Aurora, Colorado, United States

Sponsorship not specified$60k-$70kDetected 20 days ago

GCPExcelHRClinical TrialsClinical ResearchFDA RegulatoryResearchCommunicationProblem SolvingAdaptabilityMicrosoft OfficeGxP

About the role

Are you well organized and adaptable to unexpected changes?
Are you someone who can see the bigger picture, without losing sight of the day-to-day tasks?
In this position you will: Contact study sites and schedule SEEVs as assigned.

CPC is an academic 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.
Monthly fun events (e.g. team building activities, games, charitable events, potlucks, picnics)

MUST be comfortable with travelling up to 80% of the time, and live near a major airport hub.
With over 30 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.

Bachelor's degree or nursing degree preferred.
2-4 years of experience in a clinical research setting.
Working knowledge of Good Clinical Practice (GCP) and applicable FDA and ICH regulations.
Strong organizational, communication, and problem-solving skills.
Proficiency in Microsoft Office (Outlook, Word, Excel).
Willingness to travel up to 80%, including international travel and live near major airport hub.
Ability to work independently and exercise sound judgment to appropriately escalate issues.

Contact study sites and schedule SEEVs as assigned.
Coordinate travel arrangements for domestic and international SEEVs.
Complete detailed, accurate, and timely SEEV reports and communicate findings to internal study teams.
Escalate site concerns identified during SEEVs to the appropriate Clinical Trial Manager or Project Manager.
Assist Clinical Trial Managers and CRAs with enrollment and retention escalations for international sites.
Communicate with site staff to resolve issues related to missing, incomplete, or inaccurate submissions.
Participate in discussions related to site compliance, performance trends, and corrective actions.
Serve as a supporting contact for site questions when CRAs or CTMs are unavailable.
Help ensure accurate documentation in CTMS, TMF, and other study systems.
Perform additional activities as assigned.

$60,000 - $70,000 annually
CPC is an academic 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 30 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.
Matching 401(k) plan (dollar for dollar up to 4% of your eligible compensation, fully vested immediately)
11 paid holidays

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/
Comprehensive benefits package (medical, dental, vision, life, STD, LTD etc.)
15 - 25 vacation days based on years of service
Flexible and remote work schedules

An Equal Opportunity Employer
CPC is dedicated to the principles of equal employment opportunity (EEO).
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.

This listing is sourced directly from cpc's careers page and normalized into a canonical job model.