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Clinical Research Study Coordinator

Neurology Private Practice

Plymouth, Massachusetts
  • Clinical Operations
Neurology Private Practice
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  • Research Salary

Job Details

Community neurology practice setting for Alzheimer’s disease modification and other therapy trials. FDA-approved Phase 2 and 3 multicenter clinical trials. Lovely practice setting (SE Massachusetts), well-established clinical neurology practice. Candidates with prior Study Coordinator experience only. Ours is an experienced Clinical Research site with expanding need for additional SC’s. Would be joining an existing high quality group – organized, efficient, and experienced.

Roles include customary duties for Study Subject coordination activities, as well as Regulatory duties for the Studies. Specific responsibilities include:

  • Study protocol submissions to Institutional Review Boards (IRB).
  • Recruiting subjects to the trial using flyers, advertisements, letters, etc.
  • Working with physicians, imaging facilities/technologists. Pharmacists, lab staff, CRAs, Sponsors, potential and enrolled subjects, working knowledge of numerous relevant IT functions.
  • Assist in consenting potential subjects/participants, explaining the trial simply and answering their questions and concerns as well as checking in with them regularly to monitor compliance with the study guidelines.
  • Specific responsibilities collecting, managing and maintaining all study related paperwork and correspondence. This includes creation of paper CRF’s, uploading data from CRF’s to variousmeta-databases, responding to queries, assisting other Study personnel in responding to queries, SAE reporting, FDA paperwork (1572 forms), close working relationship with CRA’s.
  • Following the set of study guidelines set out by the International Conference on Harmonization to ensure the trial is carried out using Good Clinical Practice and according to the laws of the country on how clinical trials must be conducted.
  • PT (evolving to FT) position. M-F 8-5 with flexibility during those hours to accommodate other life needs. To emphasize, candidates with prior Study Coordinator experience only.

Benefits include vacation, sick-time, 401K but not medical/dental health insurance. Fair baseline wages augmented by very generous productivity bonuses.

Job Type: Full-time

Required experience:

  • prior experience as a Study Corodinator: 3 years

Required education:

  • Bachelor's

Job Location:

  • Plymouth, MA 02360

Required language:

  • English
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