Clinical Project Manager - Clinical Consultancy

Recruiter
i Pharm Consulting Ltd
Location
Hertfordshire
Posted
12 Jan 2018
Closes
12 Feb 2018
Sector
Healthcare
Contract Type
Permanent
Hours
Full Time
Oversee clinical study teams, site activities, and clinical operations plans for international clinical trials for a leading Clinical Consultancy.

LOCATION

UK - Cambridge

ROLE RESPONSIBILITIES

The main duties and responsibilities for this position will include but not be limited to:

- Lead study start-up and site selection teams, developing site feasibility criteria and supporting evaluation and validation activities

- Manage clinical operations resource needs (CRA's and Junior PM's)

- Develop clinical operations plan and milestones and report accordingly to client Project Directors on country specific activities

- Input to training plans, monitoring plans and risk contingency plans

- Support and oversee regulatory submissions, managing affiliate partners in a number of countries

- Manage the Clinical Operations Team, ensuring productivity, precision and cohesion

- Conduct performance reviews and feedback for study teams

- Ensure all clinical operations activities are adherent of ICH/GCP, company SOPs and project plans

- Contribute to the creation of study budgets

- Work with client study director to address project issues and implement process improvements

The successful candidate will have a strong background in clinical project management, clinical study management at an international level or clinical operations management. You will be a confident leader and an excellent communicator and enjoy improving the quality of project delivery from start to finish.

ROLE REQUIREMENTS

- University degree in Life Sciences or a related field

- Previous clinical trial / project / operations management experience

- Thorough understanding of ICH Guidelines, GCP and regulatory requirements

- Ability to travel when necessary

ABOUT i-PHARM CONSULTING

i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.

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TO APPLY

If you would like to discuss this vacancy further, please call Principal Consultant Ciara Noble on Phone number removed or email Email address removed. If this role is not suitable, Ciara is also available to discuss other possible positions or answer any general questions regarding your career and the current market.