Clinical Project Manager - Scotland
Location: Edinburgh Scotland
Description: Novella Clinical Resourcing is currently seeking to employ Clinical Project Manager - Scotland right now, this career will be placed in Scotland. For detail informations about this career opportunity kindly see the descriptions. Job Summary:
Excellent office based project management opportunity in Scotland, working with a World leading Global Pharmaceutical company.
Requirements:
Requirements:
CLINICAL PROJECT MANAGER (Pharma, Scotland)
Our client is a global medical device company, and has been a leader in surgical sutures (stitches) for more than 100 years. Today, our client have expanded it’s expertise into wound management, women`s health, and cardiovascular surgery. Our client enjoys a reputation for developing quality products to enhance the lives of patients and for providing outstanding service to customers. Headquartered in New Jersey, our client presently conducts business in 50 countries and employs approximately 9,000 employees in its various worldwide locations.
Principal Duties and Responsibilities for the clinical project manager will include;
Frequent inter-organizational and outside contacts with medical consultants in planning, implementing and facilitating assigned studies.
Assisting in planning, design, management of monitoring activities and reporting of clinical studies.
Providing upper management with study updates.
Assisting in design of study budgets and financial arrangements with investigators.
Coordinating and conducting group investigator meetings.
Assisting in interpretation of clinical study data.
The Project Manager will be instrumental in development of study documentation, investigator’s brochure and publication plan.
Assisting in development of clinical section of Regulatory submissions, as needed.
Education and/or Experience
Bachelor’s degree in Biological Science or nursing qualification and related scientific/technical experience or Masters degree in a scientific discipline and related scientific/technical experience or
Masters degree with thesis and related scientific/technical experience
Previous experience working in a CRA and/or Clinical Project Manager role
Medical Device trial experience would be highly advantageous
Other Skills and Abilities
Must have a sound working knowledge of preclinical and clinical research, familiar with requirements and current attitudes of regulatory agencies, and have technical writing capability.
Works on a wide variety of problems relating to clinical studies, such as protocols, resolving problems with progress of investigators, grant application and remuneration.
Must be extremely flexible and able to change priorities rapidly
Must be computer literate (Microsoft Windows, Word, Excel, Power Point)
GCP, CFR, ICH and ISO knowledge required
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If you were eligible to this career, please email us your resume, with salary requirements and a resume to Novella Clinical Resourcing.
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This career starts available on: Fri, 06 Jul 2012 14:41:58 GMT