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PROJECT MANAGER

COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries.

You can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Our commitment to this mission has resulted in Covance’s impressive history of company stability and growth. We’ve achieved these results by fostering a work environment that encourages, develops and leverages our team’s capabilities.
This is your chance to become part of a team that helps to bring miracle of medicine to market sooner.

This role can be based in one of our office's in Europe or home based.

About the Job

• • You will be the lead & main point of contact on Phase I & IIa clinical trials
• You will have direct client contact & will work closely with them on project timelines
• You will have full responsibility for resourcing and budget management
• You will be a key member of bid defences

About You

You should typically be qualified to degree level or equivalent in one of the life sciences
• Ideally, you will have extensive experience as a Clinical Project Manager
• Phase I & IIa experience is a must
• You must have budgetary & financial management experience
• You must be client focused & have excellent communication skills
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. (M/F/D/V). Your confidentiality and privacy are important to us.
Required: EUROPE
• Current Institute of Clinical Research status: Professional Member level.
Required: USA and EUROPE
• Life Sciences degree. Licensure and experience may be substituted for educational requirements.
• Advanced knowledge of ICH guidelines, CFR, GCP and the clinical trial process.
• Advanced knowledge of project management processes.
• Demonstrated ability to manage complex clinical projects with minimal supervision.
• Ability to work within and lead a project team.
• Ability to work with other Covance business units.
capabilities with clients.
• Basic understanding of statistical programming, data management, and clinical trial report preparation processes sufficient to perform project management responsibilities.
Typically 5-6 years of research experience.
• 2-3 years project/study management experience.
• Additional experience may be substituted for education requirements..
To apply for this position please contact the Covance website directly on. www.covancecareers.com
Quoting reference no:26152.