Study Management Associate

Highly Competitive Salary
  1. Permanent
  2. Clinical Trial Assistant (CTA), Project/Study Manager (CSM/CPM), Clinical Scientist
  3. United States
Atlanta, USA
Posting date: 22 Jan 2021
CR.BC.35217

Proclinical is currently recruiting for a Study Management Associate with a biopharmaceutical company located in Atlanta, GA.

Job Responsibilities:

  • Responsible for executing one or more elements of clinical studies in compliance with quality standards
  • Supports the Study Project Manager in leading the cross functional study team
  • Supports the preparation of Clinical Study Team meetings (Agenda/Minutes)
  • Responsible for regular updates to the cross-functional team and stakeholders on study status; ensure our CTMS is up to date
  • Supports the development of the clinical study blueprint/protocol and associated systems and documents (Informed consent forms, eCRFs, IRT, CSR)
  • Supports the vendor selection, scope development, management and oversight of external vendors
  • Responsible for generating the study related training for the study team, study sites, and vendors for assigned studies
  • Proactively identify and resolve and/or escalate study related issues

Skills and Requirements:

  • Bachelor's Degree
  • Scientific and/or Healthcare field, equivalent is required
  • Associate degree must have RN degree with relevant experience is acceptable.
  • Must have at least 2-8 years of Pharma-related/clinical research related experience and demonstrated a high level of core and technical competencies.
  • Possesses good communication skills.

If you are having difficulty in applying or if you have any questions, please contact Bri Copeland at 267-297-3280.

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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