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UBC - Sr Project Manager - Clinical Research

Company Name:
Express Scripts
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ABOUT EXPRESS SCRIPTS
Advance your career with the company that makes it easier for people to choose better health.
Express Scripts is a leading healthcare company serving tens of millions of consumers. We are looking for individuals who are passionate, creative and committed to creating systems and service solutions that promote better health outcomes. Join the company that Fortune magazine ranked as one of the "Most Admired Companies" in the pharmacy category. Then, use your intelligence, creativity, integrity and hard work to help us enhance our products and services. We offer a highly competitive base salary and a comprehensive benefits program, including medical, prescription drug, dental, vision, 401(k) with company match, life insurance, paid time off, tuition assistance and an employee stock purchase plan.
Express Scripts is committed to hiring and retaining a diverse workforce. We are an Equal Opportunity Employer, making decisions without regard to race, color, religion, sex, national origin, age, veteran status, disability, or any other protected class. Applicants must be able to pass a drug test and background investigation. Express Scripts is a VEVRAA Federal Contractor.
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ABOUT THE DIVISION
United Biosource Corporation is the leading provider of integrated development and commercial support solutions that deliver evidence of safe use, while optimizing access to mediation and care.
UBC leverages our specialty pharmacy therapy expertise and contracts for specialty pharmacy and specialty distribution services.
## JOB DESCRIPTION
Brief Description:
Accurate reporting and interpretation of project metrics
Proposal and implementation of action plans
Satisfactory delivery of contracted services and achievement of contracted milestones for assigned projects
Financial integrity of assigned projects
Supervision of assigned project staff
Supervisory Responsibilities:
Supervise project management staff in execution of assigned studies
Prepare PMs to make presentations to clients in defense of proposals
Ensure that the PM understands the client needs once a project is awarded
Serve as a resource and mentor to the Project Manager in the execution of their daily activities
Proactively assist the PM in anticipating and seeking resolutions to potential and actual project issues
Specific Job Duties:
Serve as the primary contact with the sponsor for all study related items, with oversight of all aspects of trial conduct, from study start-up through close-out in accordance with company and project specific SOPs, guidelines, budgets, timelines and contracts
Assist in the development and design of protocols, CRFs, regulatory documents, study master file, and other study related deliverables
Ensure operational plans are developed consistent with program needs, including but not limited to, the development of communication plans, monitoring plans, project plans, training plan, study timelines and clinical management plans; monitor project progress as compared to established plans and ensure compliance with plans
Facilitate and plan investigator meetings; recruit qualified investigators and assist in budget negotiations
Supervise monitors to ensure site visits occur as scheduled and trip reports are accurate and timely; reports to the Sponsor on study progress
Supervise other staff assigned to programs, including clinical site specialists (CSS) and regulatory associates (RA)
Ensure project training occurs
Serve as a resource to team members for all inquiries and issue resolution for site management, contract budget and remediation, and regulatory document preparation
Lead internal client teleconferences and/or meetings and present study information at client meetings, bid defenses and UBC monthly project review meetings
Assist in preparation of client proposals in response to RFPs
Ensure project budget is tracked against contract milestones
Duties described for Project Manager and other duties as assigned by management
LI-CW2-UBC
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Qualifications:
Bachelors degree or equivalent experience
At least 5 years of clinical trial experience
Very good supervisory skills
Very good interpersonal skills
10% travel
Job Category: Research & Clinical Services
Primary Location: United States-Pennsylvania-Blue Bell
Other Locations: United States-Missouri-Kansas City
Work Locations: Blue Bell, PA - 920 Harvest Drive (4907)920 Harvest DriveBlue Bell, 19422Kansas City, MO - 3822 Summit Ave (3613)3822 Summit AveKansas City, 64111
Schedule: Full-time
Shift: 1st Shift
Employee Status: Regular
Travel: Yes, 10 % of the Time
Work From Home?: Yes

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