Clinical Project Manager (PM)

Labcorp

Place of work
Finland
Contract type
full-time

Information about the position

Job description, responsibilities and duties

At the moment we are looking for Project Manager (PM), Finland (home based)


About this role

The position holder manages and is responsible for all aspects of assigned Phase II - IV global and complex local clinical trials from the study concept to the clinical study report according to standards set by the Sponsor and applicable regulatory and legal requirements.

The main objectives are to leads a global, cross-functional Study Team for the entire duration of the study and manage the planning, implementation, analysis and reporting of assigned studies within the established timeframes and budget, with the quality and requirements necessary for global regulatory approvals.

Employee perks, benefits

We Offer
Covance’s ongoing success offers team members unsurpassed growth and career development opportunities.
At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career.

There is no better time to join us!

Covance is committed to diversity in the workplace and is an equal opportunity employer. Your confidentiality and privacy are important to us.

Information about the selection process

To learn more & apply
To learn more and apply, please visit www.covancecareers.com and search for the reference 50987BR, or follow the link:
http://jobsearch.covance.com/jobs/1101856-Project-Manager.aspx



Key words:

Project management, clinical research, oncology, Finland, PM, APM, associate project manager, clinical project manaeger.

Requirements for the employee

Candidates with education suit the position

University education (Master's degree)

Language skills

English - Intermediate (B1)

Personality requirements and skills

About you

Bachelor’s degree or equivalent education with 7 -8 years of relevant healthcare experience and 3 years clinical operations experience in the pharmaceutical industry, 1 - 2 years of monitoring and 2 clinical study management experience is required.
Also in-depth knowledge about oncology is preferred. Proven history of finding novel solutions to challenging drug development issues and developing innovative regulatory strategies.

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Brief description of the company

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ID: 2018243  Datum zveřejnění: 18.2.2015