Ref #: 28514

Employment type: Fixed term - Full-Time

Location: Remote US

Posted: 19-Apr-2021

Description

DOCS is currently seeking a Clinical Trial Manager Associate in the United States.

Responsibilities:
Establishes strong partnerships with external investigators and collaborators to ensure ongoing activities (e.g. sponsor updates, drug shipments, publications, milestone payments, etc) for CO and ISR studies are executed in a timely manner and with high quality.
- Proactively identifies potential operational challenges and in collaboration with senior team members provides resolution plans to ensure study remains on track
Establishes strong cross-functional relationships and exhibits strong leadership skills with counterparts in other functional teams (e.g., CSM, CCF, DSPH, and Medical Affairs) to ensure efficient execution of the study management processes.
- Proactively identifies potential operational challenges and in collaboration with senior team members provides resolution plans to ensure study remains on track
- Contributes to development of study budget
- May serve as a resource for others within the company for clinical trials management expertise
- Able to examine functional issues from an organizational perspective
- Participates in the recruiting and hiring process for CPA/CTMA/Sr. CTMA and support their professional development

Qualifications:
BA/BS Degree required.
Late Phase/Phase IV experience preferred
A minimum of 5 years of experience in the Pharmaceutical, Biotechnology, and/or CRO industry.

DOCS is the FSP division of ICON Clinical Research. We provide global strategic resourcing and FSP services to the biopharmaceutical and medical device industries. Founded in 1997, DOCS has grown to become the premier resourcing provider for the clinical development industry.

DOCS is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.