Interim Clinical Research Associate / CRA

Recruiter
Axess Ltd
Location
London (Greater)
Posted
12 Jan 2018
Closes
11 Feb 2018
Sector
Healthcare
Contract Type
Contract
Hours
Full Time
Our global pharma company client is looking for a CRA to join their team on a 12 month contract and provide monitoring support in late phase development across multiple therapeutic areas.

BACKGROUND:

12 month day rate contract

Office based with 40% UK travel and occasional EU travel

Global organisation - top 20 pharma

PRIMARY DUTIES

- Conduct feasibility, pre-selection, initiation, monitoring and close-out visits of company clinical studies in accordance with relative SOPs and regulations. Ensure complete and efficient exchange of information between the investigator site and company by regular on-site visits, telephone calls, email etc.
- Assure rapid retrieval of all clinical data, especially with regards to reporting of (serious) adverse events, in accordance with relevant protocol and company SOPs.
- Establish/maintain a working relationship with investigators and relevant site staff.
- Ensure high quality clinical data by detailed monitoring of data, source data verification, query resolution and maintenance of equipment etc.
- Ensure that all necessary documents are in place for release of study medication to site, monitor drug accountability at site, account for all medication (used/unused) and ultimate destruction.
- Be responsible for filing and maintenance of Site Files for assigned sites, and where relevant, Country Files (ie periodically reviews files and maintains checklist).
- Assist in MREC and R&D application for studies.
- Assure that all necessary approvals and documents are available/signed before/at site initiation.
- Liaise with CTA in preparing site payments and track payments versus schedules.
- Maintain site status in relevant CTMS and ensure training is maintained

QUALIFICATIONS / EXPERIENCE REQUIRED:

- Monitoring experience (Phase II/III or IV) preferred but an experienced CTA would be considered
- A good understanding of clinical guidelines & SOPs
- Knowledge of RAVE & IMPACT would be useful but not essential
- The ability to communicate effectively across a broad group from Medics & Patients to Investigators and internal colleagues
- A clean, current UK driving licence

Benefits:

Day rate

TO APPLY:

For a confidential discussion please telephone Sukhveer Gill at AXESS Limited on ************** To apply, please send your CV to **************** quoting reference EM-7014.

ABOUT AXESS:

AXESS has been operating since 1990

We are a recruitment business dedicated to the pharmaceutical industry, specialising in Medical Affairs, Regulatory Affairs & Clinical Development

We match professional candidates to the best permanent, contract and interim roles in the market