Clinical Trial Associate

Highly Competitive Salary
  1. Permanent
  2. Clinical Trial Assistant (CTA), Clinical Research Associate (CRA)
  3. United States
Boston, USA
Posting date: 19 May 2020
This vacancy has now expired

Proclinical is currently recruiting for a Clinical Trial Associate with a global pharmaceutical company located in Boston, MA. Successful candidate will work closely with Manager and Clinical Operations personnel to perform quality checks and file Clinical Trial Master File (TMF) to ensure high quality documentation in accordance with country-specific regulations, ICH Guidelines and Good Clinical Practices (GCPs).

Job Responsibilities:

  • Conduct quality checks of the Clinical TMF documents.
  • Work with internal functional area document owners and CRO to remediate any issues identified with Clinical TMF documents during quality check.
  • Scan, file and maintain study documentation in the Clinical Trial Master Files and in the electronic Trial Master Files system and/or applicable Records Management system.
  • Provide central support for uploading clinical TMF documents to EDMS to support key trial activities (e.g., regulatory submissions, clinical study reports etc.).
  • Work with GDO stakeholders to review and manage operational clinical trial data to ensure quality and completeness per data quality standards and specified system guidelines.
  • Provide centralized data entry support for operational systems ensuring alignment with data quality standards.
  • Review and contribute to processes and tools in support of maintaining operational and document management systems to ensure quality and completeness.
  • Review operational data to inform and document trends and risk areas to key stakeholders.
  • Support other trial related operational activities as needed and assigned.

Skills and Requirements:

  • BA/BS with 1-3 years of industry or comparable experience.
  • Some clinical research educational courses and knowledge of regulatory and Good Clinical Practice requirements preferred.
  • Understanding of the Trial Master File including understanding of the DIA TMF Reference Model preferred.
  • Experience working in electronic Trial Master File specifically Veeva Vault eTMF platform preferred.
  • Internal candidates must have demonstrated high performance in current position.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please call Mary Jacobs at (+1) 312-291-4181 or upload your resume on our website -

A full job description is available on request.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.