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Clinical Data Coordinator II Job

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Date: Jan 31, 2019

Location: Minnetonka, MN, US, 55343

Company: Boston Scientific

Additional Locations: US-MN-Arden Hills

 

 

Purpose and Passion • Comprehensive Benefits • Life-Work Integration • Community • Career Growth

At Boston Scientific, you will find a collaborative culture driven by a passion for innovation that keeps us connected on the most essential level. With determination, imagination and a deep caring for human life, we’re solving some of the most important healthcare industry challenges. Together, we’re one global team committed to making a difference in people’s lives around the world. This is a place where you can find a career with meaningful purpose—improving lives through your life’s work.

 

About this role:

The Clinical Data Coordinator II performs administrative tasks as part of Clinical Project Process and work with clinical project teams and Clinical Research Associates/Clinical Program Managers to support the completion of clinical trial documentation processes, budgets, contracts and device management (if applicable).

 

Your responsibilities will include:

  • Completion of Study Master File Index (SMFI).
  • Coordinate all translations.
  • Documentation - Receive and process (upload, assigning of attributes, filing, review and approval of subset of documents in CDC) required regulatory, legal and financial documentation in order to ensure successful study start-up (e.g. site initiation visits, product shipment, start of patient enrolment) and GCP study conduct throughout the study, following WI.  Manage study and site document archives (paper and/or electronic) as required.
  • Process clinical study payment requests for studies not in RAVE.
  • Receipt of core trial documents from all clinical functions and file in accordance with SMFI.
  • Assembly & distribution of mass communications (MOP, Study Tools, Newsletters, Annual Reports).
  • Reconcile site training files.  Monitor and report project-specific training compliance.
  • Manage site/contact/study information in BSC appropriate tools.

 

What we’re looking for in you:

Minimum Qualifications

  • 2 years with High School degree/equivalent or an equivalent combination of education/work experience
  • 2+ years of Clinical Trial Coordinator or Clinical Research Associate experience

Preferred Qualifications

  • Bachelor’s degree
  • Comfortable working with different clinical systems, knowledgeable of GCP requirements for clinical document management, knowledgeable with using Excel and PowerPoint.
  • Good communication, detailed oriented, a self-starter, driven for highest quality in all deliverables, and someone who enjoys and thrives in a team environment

 

About us

As a global medical technology leader for more than 35 years, our mission at Boston Scientific (NYSE: BSX) is to transform lives through innovative medical solutions that improve the health of patients. If you’re looking to truly make a difference to people both around the world and around the corner, there’s no better place to make it happen.

 

Boston Scientific is an Equal Opportunity Employer – Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Disability, Veteran

 

Requisition ID: 441350

 


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