Clinical Document Associate job in Boston, USA

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Last Name*

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First Name*

Last Name*

Email*

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Are you an employer or a jobseeker?*

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First Name*

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Job type: Permanent

Discipline: Clinical Trial Assistant (CTA), Clinical Research Associate (CRA)

Location: United States

This vacancy has now expired. Please see similar roles below...

Proclinical is currently recruiting for a Clinical Document Associate with a CRO located in Boston, MA. As the Clinical Document Associate, you will support the clinical trial team and other areas as needed

Job Responsibilities:

Synthesizing data from Veeva Vault, Clincase (CTMS), and other systems to design and prepare reports analyzing document compliance across numerous of KCR's clinical trial studies
Preparing, maintaining, and updating Trial Master Files for various international clinical trial studies
Performing high-level administrative review of clinical trial study TMFs
Liaising daily with KCR functional area project team members such as CRAs, project managers, and data science associates
Assisting in KCR pharmacovigilance activities as needed
Applicable software:
- Veeva Vault Platform
- Veeva Clinical Suite
- Clincase CTMS
- Argus (Oracle)

Skills and Requirements:

BSc required.
Must have an interest in the clinical research area, but it can be a relatively entry-level person
Early on/entry-level in career who is looking to get experience working in clinical studies.

If you are having difficulty in applying or if you have any questions, please contact Anabel Balsebre at (+1) 646-779-7965 or a.balsebre@proclinical.com.

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.

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