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Career Openings


Sr. Clinical Research Coordinator

ID: 1451
Department: Clinical Operations
Location: Cambridge Headquarters
# of Openings: 1

Description

Functional area: Clinical Operations

 

Position description:

We are seeking a motivated and enthusiastic clinical research professional interested in joining our fast-paced company to support multiple clinical research studies. The primary responsibility of the Senior Clinical Research Coordinator will be to maximize the operational efficiencies in Phase 1–4 clinical trials.

 

Responsibilities:

  • Collaborates closely with Ironwood Clinical Study Leads, study teams, and CRO partners;

  • Supports implementation and management of clinical research studies through file management and clinical project document control;

  • Assists the Ironwood clinical project teams in project related activities, such as creating study binders, shipping study documents, and drafting newsletters;

  • Reviews and tracks clinical trial regulatory documents;

  • Assists in the planning and preparation for investigator meetings;

  • Maintains study tracking tools and study calendars;

  • Works closely with Ironwood Records Management, Ironwood Regulatory, and CROs to ensure adequate clinical trial documentation;

  • Completes telephone logs, notes to file, and status reports;

  • Participates in study team meetings and drafts meeting minutes and agendas;

  • Some travel may be required.

 

Qualifications:

  • B.S. / M.S. or equivalent;

  • At least 2 years experience in a biopharmaceutical, contract research organization, or hospital setting participating in the conduct of clinical trials;

  • Superior understanding of Microsoft Office products;

  • Aptitude for organizational detail;

  • Capacity to complete tasks independently in a highly-regulated environment;

  • Flexibility to function well within a team environment and within condensed timelines;

  • Ability to verbalize complex study issues and demonstrated problem-solving ability;

  • Basic understanding of FDA regulatory requirements and good clinical practice (GCP).


Ironwood is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.





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