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Vacancy details
Vacancy description:
Job Code:
(Senior) Project Manager
Job Title:
(Senior) Project Manager
Job Category:
CRM (Clinical Research Management)
Contract:
Permanent
Discipline:
Any Discipline
Country:
Czech Republic
Location:
Any Location
Min experience:
N/A
Annual salary:
Negotiable
Apply by:
05 Jul 2008
(Senior) Project Manager
Qualifications: 4-year or equivalent college degree from an appropriately accredited institution, preferably in science or nursing or applicable industry-related experience; three years clinical trial experience, preferably including monitoring as a Senior or Lead CRA, clinical auditing, clinical data management, Lead CRA or study coordinator experience.
one year experience in a team-oriented, collaborative environment, preferably with supervisory/lead responsibilities.
Appropriate qualifications in life sciences, pharmacy, medicine or nursing with clinically related experience.
Fluency in verbal and written English.
Specialized Training, Skills and Abilities Working knowledge of clinical research procedures and practices including local regulations, GCP/ICH Guidelines and relevant local regulatory requirements for the conduct of clinical development programs.
Excellent organizational, communication and interpersonal skills.
The ability to work independently and to motivate and lead a team.
Business orientation for conducting projects in timely and cost-effective manner.
Must be familiar with project management tools/applications.
Must be proficient in computer use.
Must possess the ability to travel independently by air, car and/or train.
Up to 30% travel, 70% work in office environment.
Responsibilities: The Project Manager is responsible for the day-to-day cross-functional operations of the assigned study or studies for one or more clients. As the team leader, the Project Manager will ensure assigned studies are delivered successfully, on-time, within budget, according to client expectations and with the highest level of quality possible. The Project Manager may manage any combination of the following: single or limited services study, a small regional cross-functional study or manage a portion of a larger global study. Some other responsibilities include:
In a matrix environment, manage, lead and motivate the assigned cross-functional project team, facilitating the team’s ability to fulfill their responsibilities in accordance with project contracts, contract amendments and Omnicare Clinical Research policies, procedures and SOPs.
To develop and maintain close working relationship with the client’s study management team(s) to ensure client satisfaction, operational and customer service excellence.
To ensure successful design, implementation, tracking and maintenance of project plans for assigned projects; manage day-to-day operational aspects of assigned projects including third party vendor activities.
To plan, participate and present at investigator meetings, as required.
Function as primary liaison between client, third party vendors and Omnicare Clinical Research project team for project issues, including initiation, planning, execution and close-out of assigned studies.
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