**ON-SITE POSITION IN FOXBOROUGH, LOOKING TO ATTRACT LOCAL TALENT. TWO YEARS OF CLINICAL RESEARCH EXPERIENCE PREFERRED AND A BS/BA IN SOCIAL OR BIOLOGICAL SCIENCES**
The Neurology Center of New England, a multi-specialty neurology center located centrally in Foxboro, MA, is looking for a highly motivated Clinical Research Coordinator (CRC I) to join our research team and contribute to the administration of industry-sponsored clinical studies for the treatment of Multiple Sclerosis, Parkinson's Disease, Alzheimer's disease, migraine, and other neurological conditions. This qualified candidate will be working in collaboration with, and directly under the supervision of, the Lead Clinical Research Coordinator and Clinical Research Manager. The position is ideal for someone who wishes to continue to build their clinical research skills in a positive, fast-paced, and collaborative environment. Essential Job Functions will include (but not remain limited to):
- Ensuring adherence to appropriate protocols in the recruitment, screening, enrollment, treatment, follow-up, discharge, and retention of study patients in accordance with Good Clinical Practice (GCP) and ICH Guidelines. Have working knowledge of all study protocols and availability to serve as a backup coordinator and/or rater for other studies as needed
- Recruiting subjects into clinical research trials, including but not limited to conduction of chart reviews in EMR system, pre-screening calls to review eligibility, meetings with subjects to review eligibility criteria at screening visits, updating eligibility spreadsheets to track status of candidacy, etc.
- Performing clinical duties as required, including but limited to blood collections, EKG administration, functional outcome assessment administrations, and medication and medical history review
- Assisting with collection, shipment, processing and handling of laboratory specimens
- Dispensing, administering, and/or preparing IMP as required per protocol. Maintain accurate and organized master and subject-level IMP accountability logs. Ensure proper IMP storage and destruction procedures are followed according to site SOP and study protocols
- Maintaining investigator site file (ISF) and IMP binders
- Communicating with study Sponsors and study monitors to ensure appropriate subject data management and conduction of protocols
- Scheduling subject initial and follow-up appointments, monitoring visits, and other essential appointments as needed
- Offsite duties: limited travel to investigator meetings and other sponsor-related events
- Interest in manuscript writing/editing to prepare for submission to research journals and scientific meetings (as applicable)
- Abiding by all OSHA, HIPAA compliance, and GCP requirements and perform responsibilities in an ethical manner consistent with NCNE values, policies, and procedures
Required Education & Experience:
- 1-2 years of clinical research experience or related clinical research positions or equivalent experience preferred
- BS / BA in social or biological sciences, or an equivalent combination of education and experience in a health-related field
- Phlebotomy skills (e.g. ECG administration, vital signs collection, blood collection) preferred but not required
Job Type: Full-time
Pay: From $45,000.00 per year
Benefits:
- 401(k)
- Dental insurance
- Employee assistance program
- Health insurance
- Paid time off
- Vision insurance
Experience:
- Clinical research: 2 years (Required)
- Phlebotomy: 1 year (Preferred)
Ability to Commute:
- Foxborough, MA 02035 (Required)
Work Location: In person
