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Job Details

Clinical Study Manager - Midlands

Company: i-Pharm Consulting
Location: Derbyshire
Reference: SOAR994
Closing Date: 19 Jan 17
Type: Permanent
Salary (£): Negotiable
Benefits:

Job Summary:

Clinical Study Manager - Midlandsi-Pharm consulting are partnering with a leading academic institution to appoint a Clinical Study Manager in their clinical R & D department. The clinical study manager will be responsible for the set-up, delivery and close out of clinical trials in line with GCP, governance frameworks, budgets and timelines. ...

Requirements:

Clinical Study Manager - Midlands

i-Pharm consulting are partnering with a leading academic institution to appoint a Clinical Study Manager in their clinical R & D department. The clinical study manager will be responsible for the set-up, delivery and close out of clinical trials in line with GCP, governance frameworks, budgets and timelines.

As Clinical Study Manager, you will work with research leaders to develop funding applications and act as the point of contact for a variety of stakeholders on the management and progress of clinical trials.

You will ensure that the day to day management of your assigned studies is in adherence with research governance guidelines and that smooth cross functional communication is facilitated with other research team members such as QA, Data Management, Statisticians and other clinical administration staff.

Core study related responsibilities will include:

• Site initiation and training of site staff
• Development of monitoring plan
• Develop study procedures in line with departmental SOPS
• Production of relevant study documentation in line with HRA and Ethical guidelines
• Support investigators to ensure studies are in-line with governance and legal outlines
• Oversee and monitor multiple studies simultaneously

The ideal candidate for this role will first and foremost be an outgoing clinical research professional and will have an existing in-depth knowledge of GCP, EU Regulatory standards. You will have existing experience in co-coordinating multicentre trials, line management and reporting. You must also hold a relevant scientific degree or nursing qualification.
This is an exceptional opportunity for an experienced study manager / coordinator to join one of the country’s most recognised research facilities. You will have the opportunity to develop your trials management skills as the department continues to grow and move through a large pipeline of development projects.

TO APPLY

If you would like to discuss this vacancy further, please call Principal Consultant Sophie Ahern on +44 (0)20 3189 2297, or email sahern@i-pharmconsulting.com. If this role is not suitable, Sophie is also available to discuss other possible positions or answer any general questions regarding your career and the current market.

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.

www.i-pharmconsulting.com

KEY WORDS

Clinical Team Leader / Clinical Leader / Clinical Manager / Clinical Team Manager /Clinical Project Manager / Clinical Operations Manager / Clinical Operations Leader / Project Manager / CRO / Biotech / Pharmaceutical Company / Study Team Leader

Apply for this job: Clinical Study Manager - Midlands

Contact Information:

Address:  Head Office
212 New King’s Road London
SW6 4NZ
England
Reasons to work for i-Pharm Consulting
Tel:  +44 (0) 20 3189 2299
Website:  Visit Our Web Site

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