Clinical Research Associate

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  • As an Equal Employment Opportunity Employer, DAVIS has reporting requirements which require us to invite employees to voluntarily self-identify their race/ethnicity. Submission of this information is voluntary and refusal to provided it will not subject you to any adverse treatment. The information obtained will be kept confidential.
  • By applying to this position and providing my contact information, I give The DAVIS Companies permission to provide me with email communications and information.

Clinical Research Associate

  • Specialty:

    Scientific
  • Title:

    Clinical Research Associate
    • City:

      Marlborough
    • State:

      MA
    • Zip Code:

      01752
  • Start date:

    08-16-2017
  • Status:

    Closed
  • Assignment Type:

    Contract To Hire
  • Job Id:

    43197

Description

Our Client is searching for a Clinical Research Associate located in Marlboro, MA. 

Responsible for supporting the initiation, monitoring, and closing out of clinical study sites for assigned projects in order to ensure study milestones are met. Central point of communication and document control between our client and investigational sites for all clinical trial related activities.

ESSENTIAL FUNCTIONS:

  • Conducts site initiation, interim monitoring and close out visits at assigned clinical sites and continues to train study personnel as needed on eCRF completion and study procedures.
  • Maintains Trial Master Files to internal standards and regulatory requirements.
  • Resolves queries of eCRF data with study site personnel.
  • Creates CDAs and assures fully executed forms are returned.
  • Creates and maintains project specific spreadsheets as directed by project management.
  • Maintains tracking and reconciliation of investigator payments.
  • Assists other team members with site-specific issues, acting as liaison between study staff and project staff.
  • Attends and records minutes for internal Clinical meetings.
  • Prepares presentations with advanced skills in PowerPoint.
  • Conducts feasibility survey of potential sites via email or telephone.
  • Follows all company safety policies & other safety precautions within work area.
  • Regular attendance and timeliness is essential.

QUALIFICATIONS:

  • Bachelor’s degree or equivalent experience supporting clinical trials for medical devices diagnostics, or pharma
  • Minimum 1 to 2 years’ experience as a CRA required.  Previous monitoring experience required. 
  • Understanding of management of clinical site activities with knowledge of when to escalate issues to management or clinical team
  • Excellent oral and written communication skills.
  • Advanced computer proficiency, especially MS Office
  • Ability to multi-task and prioritize projects, site questions, and clinical team inquiries while managing responsibilities and deadlines.

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