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Job Details

Clinical Project Manager

Company: ClinTec International Ltd
Location:
Reference: UKPM - 110117 - KB
Closing Date: 12 Feb 17
Type: Permanent
Salary (£): Competitive
Benefits:

Job Summary:

ClinTec International is actively recruiting for a Clinical Project Manager to join our expanding global company in the UK– this is a Permanent opportunity ideally based within out HQ Office in Glasgow however we can consider candidates anywhere in the UK and home based working. By working for ClinTec you can further your career in a dynamic, fast-paced environment and you can be assured of rewarding benefits.

Requirements:

Clinical Project Manager - Scotland / UK based

ClinTec International is actively recruiting for a Clinical Project Manager to join our expanding global company in the UK– this is a Permanent opportunity ideally based within out HQ Office in Glasgow however we can consider candidates anywhere in the UK and home based working. By working for ClinTec you can further your career in a dynamic, fast-paced environment and you can be assured of rewarding benefits. 

Role Description

The Clinical Project Manager will be responsible for leading for one or more clinical trials simultaneously and be responsible for the initiation, conduct and reporting of clinical trials or programmes. The Senior Project Manager will ensure by co-ordination of project team activities that these projects are completed on or below budget, on or ahead of time and on target, according to the requirements of the contract with the Sponsor and ensure that project activities are executed according to the quality standards defined by appropriate procedures and by ICH GCP.

Responsibilities of the Clinical PM:

Supervise and evaluate the project management team and conduct of clinical trials to ensure the accomplishment of established goals and objectives
Manage and coordinate project team activities to ensure consistently high performance across the ClinTec project portfolio to the satisfaction of the client(s)
Contribute to the development of new systems to facilitate management of projects and department operations
Monitor and review the clinical studies in terms of financial progress, business metrics, KPI’s and compare to milestones delivered
Provide timely input into monthly internal program management project status reviews
Develop project schedules of tasks with input of project team members; identify responsible parties, staffing needs, and timeframe for completion of project with list of deliverables, plan timeline in concert with client commitments
Identify impending obstacles to the successful completion of the project, analyses information and develop innovative solutions to challenges
Serve as a mentor to Project Managers including the facilitation of their training and orientation and as a resource for administrative and project related issues
Participate as required, in proposal development, business development, and client presentations and be available to present department responsibilities and functions to potential clients
Participate in development and implementation of department training programs where required

Essential Criteria:

Significant track record within clinical project management
Previous CRO experience, ideally with a CRA background
Excellent knowledge of the pharmaceutical product development process and broad therapeutic exposure including Oncology and Rare Diseases
Bachelor’s degree, equivalent of higher qualification in a relevant life sciences discipline
Clear understanding of contracts and scope of work
Ability to demonstrate strong commercial business acumen
Ability to work to strict operational deadlines and manage conflicting priorities accordingly
Excellent communication skills including the ability to interact and manage relationships with international colleagues and clients orally and in writing
High level of IT literacy including use of Internet, email and Microsoft Office suite of packages
Willingness and ability to travel internationally on a regular basis
Fluency in English language (written and spoken)
Full proof of right to work in UK

Desirable Criteria:

Formal Project Management Training / Accreditation 

Company Information:

ClinTec International is a UK-based, dynamic privately owned full service Contract Research Organization with a presence in over 43 countries worldwide.  We have been providing clinical research support services to clients in the pharmaceutical, biotechnology and medical device industries for over a decade and assist in their key product development efforts. At ClinTec International, we pride ourselves on delivering high quality, flexible and professional services/solutions for our clients.  ClinTec International has a wealth of experience in managing clinical trials in all major therapeutic areas including oncology, neurology, cardiovascular, psychiatry, infectious disease, rheumatology, immunology, respiratory and gastroenterology.

ClinTec employees can expect to receive expert training and guidance throughout their careers as well as the opportunity to be involved in every aspect of Clinical Trials across the full life-cycle of the drug development process.  We have strong partnerships with some of the world's leading pharmaceutical companies and employees can expect to be involved in some of the most prestigious drug development projects - with the opportunity to develop, progress and travel globally. ClinTec International offers a competitive salary and rewards package.

Apply for this job:  Clinical Project Manager

Contact Information:

Address:  Head Office
Clintec International Ltd,
133 Finnieston Street,
Glasgow
G3 8HB
Scotland
Reasons to work for Clintec
Tel:  +44 (0) 141 226 1120
Fax:  +44 (0) 141 248 8993
Website:  Visit Our Web Site

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