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Clinical Research Coordinator
- Permanent
- Clinical Scientist, Clinical Outsourcing, Clinical Evaluation
- United States
This vacancy has now expired. Please see similar roles below...
Proclinical seeking a Clinical Research Coordinator for a leading pharmaceutical company located in Monterey, CA.
Must be eligible to work in the US.
Job Responsibilities:
- Interface directly with the healthcare providers and patients.
- Obtain informed consent for NPM's clinical trials.
- Assist and participate in the site clinical trial initiation and all aspects of clinical trial(s).
- Ensure adherence to study protocols, data completeness and patient consent.
- Assist in patient recruitment strategies where appropriate.
- Foster collaborative relationships by effectively communicating with clinical site staff, internal stakeholders, and NPM - seen as an invaluable team member.
Skills and Requirements:
- 3+ years of experience in oncology clinical research and/or oncology ambulatory care
- Certified Clinical Research Coordinator, Associate or Professional (CCRC, CCRA or CCRP) preferred
- Bachelor's degree, focused in health science or related field preferred
- Bilingual in Spanish is a plus
- Sound knowledge of clinical trials, study-specific operating procedures and patient consent forms
- Strong desire to drive a paradigm change in clinical research conduct and improve patients' lives
If you are having difficulty in applying or if you have any questions, please contact Brianna Copeland at +(1) 267-297-3280 or b.copeland@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
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