Study Management Associate job in Atlanta, USA

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First Name*

Last Name*

Email*

Phone Number*

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First Name*

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Phone Number*

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Job type: Permanent

Discipline: Clinical Trial Assistant (CTA), Project/Study Manager (CSM/CPM), Clinical Scientist

Location: United States

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

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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