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Beacon Clinical Research is a Phase II - III independent clinical research site located in Brockton MA, about 25 miles south of Boston. We are seeking either a part- or full-time clinical research coordinator to serve for one to two years, managing pharmaceutical studies in internal medicine, dermatology, urology, psychiatry, and allergy.
CRCs serve as primary and back-up coordinators on a range of drug studies and are responsible for all facets, with about 12-18 patient visits per week. At Beacon Clinical, CRCs perform the following tasks:
* Mastering the protocol governing studies
* Managing subject visits, including consenting, gathering data, outreach calls, and scheduling
* Maintaining subject data in source documents, including documenting adverse events and submitting relevant documents to the Institutional Review Board
* Interfacing with pharmaceutical monitor, sponsor, auditors, etc.
* Front desk support (scheduling, reminder/follow-up, copy/print/fax)
* Labs/vitals/EKG/histories
* Data entry
All CRCs are expected to manage their own studies, collaborate with peers, accept feedback, pursue self-improvement through on-the-job and off-site learning and refinement, and at all times maintain and preserve the company's reputation and integrity.
If you feel that this position may be right for you, please submit resume and cover letter, detailing your background, interest, and future plans, to the following:
Beacon Clinical Research, LLC
Gabrielle Lewis, Director of Clinical Operations
45 Pearl Street, Suite B & C
Brockton MA 02301
Direct: (774) 462-6609
Main: (774) 462-6610
Fax: (774) 462-6611 NEW
[email protected]www.beaconclinical.com
CRCs serve as primary and back-up coordinators on a range of drug studies and are responsible for all facets, with about 12-18 patient visits per week. At Beacon Clinical, CRCs perform the following tasks:
* Mastering the protocol governing studies
* Managing subject visits, including consenting, gathering data, outreach calls, and scheduling
* Maintaining subject data in source documents, including documenting adverse events and submitting relevant documents to the Institutional Review Board
* Interfacing with pharmaceutical monitor, sponsor, auditors, etc.
* Front desk support (scheduling, reminder/follow-up, copy/print/fax)
* Labs/vitals/EKG/histories
* Data entry
All CRCs are expected to manage their own studies, collaborate with peers, accept feedback, pursue self-improvement through on-the-job and off-site learning and refinement, and at all times maintain and preserve the company's reputation and integrity.
If you feel that this position may be right for you, please submit resume and cover letter, detailing your background, interest, and future plans, to the following:
Beacon Clinical Research, LLC
Gabrielle Lewis, Director of Clinical Operations
45 Pearl Street, Suite B & C
Brockton MA 02301
Direct: (774) 462-6609
Main: (774) 462-6610
Fax: (774) 462-6611 NEW
[email protected]www.beaconclinical.com