Senior Clinical Project Manager

Madison  ‐ Onsite
This project has been archived and is not accepting more applications.
Browse open projects on our job board.

Keywords

Description

We are looking for experienced Senior Clinical Project Managers in the Midwest area to lead a team for a stable multi-national company in Wisconsin. This is an exciting opportunity for a self-motivated person who is looking to grow. Offering a competitive salary with great benefits and also a relocation package. Must have previous experience in Project Management at a pharmaceutical, medical device or biotech company.

The Senior Project Manager will manage one or more projects that may be regional or global in scope. The Senior Project Manager will lead cross functional project teams to ensure quality deliverables that are on-time and within budget. The Senior Project Manager will be responsible for the planning of project activities, development of the project plan and reporting of progress.

* Ensure that all allocated projects are carried out in strict accordance with the relevant protocols, analysis plans, SOPs, and the specified standards of GCPs
* Clarify specific requirements from clients
* Communicate on a regular basis with assigned clients regarding questions, concerns, and project status. Anticipate Sponsor needs for assigned projects
* Anticipates and identifies operational and logistical challenges and solutions
* Organize, chair, and record minutes for all relevant project meetings
* Facilitate meetings with Sponsors and develop/maintain working relationships with client companies
* Ensure the relevant personnel are kept informed of problems that may affect the project performance
* Coordinate receipt and inventory of study related information. Ensure all appropriate documentation and procedures are performed upon project completion

* Liaise with Quality Assurance regarding regulatory compliance of study reporting and Sponsor audits
* Elicit and coordinate interdepartmental communication
* Document and circulate client interactions
* Communicate with the Data Management, Programming, Statistics, Pharmacokinetics, Medical Writing, and QA departments regarding study progress and reporting requirements
* Update the timelines for allocated projects in a timely manner. Renegotiate timelines as appropriate
* Responsible for timely production of deliverables
* Liaise with external data vendors as appropriate with regard to the schedules of data availability
* Liaise with the Sponsor over documentation required for the report preparation process

Job Requirements/Education
  • Minimum BS/BA four (4) year degree (preferably in science)
  • At least 4 years experience in Project Management
  • Strong customer service skills
  • Excellent written, verbal, and interpersonal skills
  • Strong planning, organizational, and problem solving skills.
  • Demonstrated a high degree of initiative and ability to work collaboratively


To find out more about Real please visit www.realstaffing.com
Start date
10/2013
From
Real Staffing
Published at
14.09.2013
Project ID:
598380
Contract type
Permanent
To apply to this project you must log in.
Register