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Vacancy details
Vacancy description:
Job Code:
14052
Job Title:
Clinical Project Manager - Oncology
Job Category:
CRM (Clinical Research Management)
Contract:
Permanent
Discipline:
Clinical Project Manager
Country:
United Kingdom
Location:
Any Location
Min experience:
N/A
Annual salary:
Negotiable
Apply by:
04 Sep 2008
This is an outstanding opportunity for a candidate with previous Oncology experience to work for a niche CRO that offers a full range of drug development services specialising in the Oncology therapeutic area. They have an immediate need for an experienced Clinical Project Manager to take over a Phase III trial and would also consider a Lead CRA who has previously undertaken PM responsibilities. This role can be home based anywhere in the UK.
JOB ROLE: The Clinical Project Manager (CPM) will coordinate and manage a Phase III clinical study and staff, ensuring all time-frames and targets are met and costs are kept under control, adhering to ICH/GCP, SOPs and all regulatory requirements.
PRINCIPAL RESPONSIBILITIES include:
�Managing all aspects of assigned clinical trials effectively, including study preparations, site initiations, periodic monitoring, status and safety reporting.
�Ensuring that projects are delivered on time, within budget, and according to specifications and client/customer expectations.
�Monitoring the project from initiation through delivery.
�Evaluating the performance and compliance of CRAs and monitors within the project team(s), and the investigators conducting the study.
�Ensuring that current ICH-GCP guidelines and SOPs are strictly observed.
�Coordinating Investigator Meetings and study specific training for monitors and study team.
�Developing tracking systems, to review study progress.
�Routinely auditing filing systems of key study documentation.
�Providing ongoing support and advice to monitors.
�May attend co-monitoring visits to review and assess trial progress.
�Setting-up Financial Tracking and monitoring financial status of the study.
�Reviewing all company SOPs on an ongoing basis.
QUALIFICATIONS, SKILLS & EXPERIENCE:
�Degree in Life/Biological Sciences or related area.
�Experience from within a Pharmaceutical, Biotech or CRO environment is preferable.
�Substantial Clinical Project Management experience and Phase III experience.
�Experience in Oncology therapeutic area is essential.
�Background as an Oncology Nurse, or CRA in Oncology Studies is ideal.
�Good communication, interpersonal and presentation skills.
BENEFITS OF THE ROLE: This growing Company has a reputation for excellence and will always consider employment opportunities with candidates who have demonstrated oncology clinical research experience from Europe or the USA. The company has a strong track record of growth and you will be joining a team of high calibre professionals in an environment that offers excellent career development opportunities.
Fforde is a uniquely specialised recruitment agency/business for the pharmaceutical, clinical research and biotechnology sectors.
KEY WORDS: Clinical Project Manager, CPM, Project Management, Oncology, Clinical Trials, Phase III, Clinical Studies, Lead CRA, Life Sciences, Biological Sciences, Drug Development, CRO
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