cpc
Drug Supply/Clinical Trial Supply Manager
Aurora, Colorado
Sponsorship not specified$70k-$90kDetected 20 days ago
GCPForecastingExcelSupply ChainLogisticsProcurementHRClinical TrialsClinical ResearchGMPResearchLeadershipCommunicationOrganizational SkillsMicrosoft Office
About the role
- Responsible for timely and accurate provision of investigational product(s) (IP) for CPC Clinical Research clinical trials.
- This includes managing outsourcing to external vendors [Contract Manufacturing Organizations (CMOs)] to ensure labeling, packaging and shipping of IP in compliance with applicable regulations.
- It is our intention that all qualified applicants are given equal opportunity and that selection decisions be based on job-related factors.
Responsibilities
- Monthly fun events (e.g. team building activities, games, charitable events, potlucks, picnics)
Requirements
- Minimum of 4 years' experience in the pharmaceutical/biotechnology industry performing global clinical trial supply logistics/management, including supply chain and labeling
- Proficiency in Microsoft applications (Word, Excel, PowerPoint, Outlook, etc.), Electronic Data Capture systems
- 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.
- Establish and document supply chain for each project according to required scope
- Bachelor's Degree or higher in health or life sciences, preferred
- Experience interpreting clinical trial protocols and developing well-planned, accurately forecasted clinical supply forecasts
- Thorough knowledge of Good Manufacturing Practices (GMP), Good Clinical Practices (GCP), International Conference on Harmonization (ICH) Guidelines and other applicable global pharmaceutical regulations/guidelines/directives
- Demonstrated leadership capabilities, effective organizational skills, and excellent verbal and written communication
- Ability to work in a fast-paced, complex environment amongst internal and external partners
Compensation
- $70,000 - $90,000 annually
- 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 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)
- 10 paid holidays
Benefits
- Comprehensive benefits package (medical, dental, vision, life, STD, LTD etc.)
- 15 - 25 vacation days based on years of service
- Flexible and remote work schedules
Equal opportunity
- An Equal Opportunity Employer
- Applicants with disabilities may be entitled to reasonable accommodation under the Americans with Disabilities Act (ADA) and certain state or local laws.
- equal opportunity and that selection decisions be based on job-related factors.
This listing is sourced directly from cpc's careers page and normalized into a canonical job model.