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Job Details

Senior Clinical Research Associate

Company: i-Pharm Consulting
Location: Portsmouth
Reference: DW58
Closing Date: 21 Nov 17
Type: Permanent
Salary (£): Negotiable

Job Summary:

Job TitleSenior Clinical Research AssociateJob Summaryi-Pharm Consulting are delighted to advertise this exclusive Senior CRA opportunity within a niche CRO. ...


Job Title
Senior Clinical Research Associate

Job Summary
i-Pharm Consulting are delighted to advertise this exclusive Senior CRA opportunity within a niche CRO. This exciting organisation are capitalising on recent successes with the acquisition of a proven Clinical Research Associate who is looking for unrivalled career progression and a non-departmentalised modern operating culture that can propel their career into future management!

Portsmouth, England

Role Description
Our client look for ambitious professionals who thrive in challenging clinical environments and have a hunger to broaden their skills and experience. Continual growth has resulted in a permanent opening with a stimulating variety of responsibilities, which are outlined below:
- Monitor various studies in line with sponsor SOPs
- Take the lead on site selection, site initiation, routine monitoring and close-out visits in line with sponsor protocols
- Display willingness to execute additional study start-up responsibilities (feasibility, contractual negotiations, budget negotiations, CRFs)
- Ensure the integrity of ongoing data collection
- Operate within the project parameters while ensuring compliance with applicable regulatory, internal and project-specific requirements
- Assist the Senior CRA and management team in the development of study documents and site SOP
- Have an active involvement in the training of personnel, study sites and sponsors
- Participate in meeting preparation activities, attend sponsor meetings and deliver presentations to various stakeholders (e.g. investigator meetings)
- Act as the primary liaison with sponsor and sponsor-designated representatives where necessary
- Participate in internal and external project-related audits and audit-related activities where necessary
- Perform other departmental and study-related activities as needed and upon request

Role Requirements
- 2 years of independent site monitoring experience
- Relevant Life Sciences degree
- Sound knowledge of ICH-GCP regulations
- Proven adherence to ethical guidelines
- Valid driving license

- Competitive base salary
- Attractive insurance packages (life assurance, private medical insurance)
- Excellent Exposure to wider study responsibilities
- Supportive close-knit team culture
- Committed career development plans

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.


If you would like to discuss this vacancy further, please call Senior Consultant Dominic Williams on +44 (0)20 3873 7066, or email If this role is not suitable, Dominic is also available to discuss other possible positions or answer any general questions regarding your career and the current market.


Clinical Research Associate / CRA I / CRA / CNS / CTS / CTA / CTC / Cardiovascular / Oncology / West London / Office – Home based / Monitoring / Trials / Studies / Protocols / CRA II / Clinical Research Associate / Clinical Monitor / Monitoring / CRA II / Clinical Trial Monitor / Clinical Research Scientist / Senior Clinical Research Associate / Senior CRA / Southampton / Portsmouth / Bournemouth / Hampshire

Apply for this job: Senior Clinical Research Associate

Contact Information:

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

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