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Job Details

Project Manager - Clinical Trials

Location
New Haven, CT

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Scope & Impact:
The Project Manager will work with and assist more senior Project Managers in ensuring that **MEMBERS ONLY**SIGN UP NOW***.'s research projects are conducted on time and within budget. The Project Manager’s role is to provide support and assistance on a variety of project management tasks that will facilitate in successful study conduct.
Major Responsibilities:
Proficiency in leading and managing projects
Ability to influence colleagues to meet demanding project timelines
Strong project management, analytical, problem solving, strategic and organizational skills
Coordinate and be accountable for multiple tasks
Competence in written, oral and electronic communication skills
Ability to work independently as well as lead multidisciplinary teams
Ability to lead others, assign workload, organize projects, prioritize the work of others, and resolve problems that arise
Independently prepare project plans and manage various study projects, programs and manage mentor junior project managers simultaneously
Organize and hold regularly scheduled project team meetings
Responsible for coordinating the planning, execution, study set-up, and report finalization of assigned studies
Identify issues and as needed, works with the appropriate team member(s) to resolve issues affecting project scope, quality, effort, risk and timelines
Participate in the business development process including presentation of services, proposal preparation, bid defense meeting and conference attendance
Manage assigned project financials for monthly, quarterly and yearly ends, change order recognition and change in scope engagement
Qualifications Required:
BA/BS required in a scientific/medical field. Advanced degree preferred; or
At least 2-3 years of experience in project management or clinical operations
Associates degree with a minimum of 10 years experience in clinical research project management
Excellent organizational and multi-tasking skills
Excellent written and verbal skills and strong interpersonal skills required
Working knowledge of GCP and ICH regulations and guidelines and the application to the conduct of clinical research

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