Senior Clinical Trial Management Associate perm job
Posted on Jan 16, 2019 by Hays Specialist Recruitment Limited
Your new company
One of the world's largest research-based biopharmaceutical companies that discovers, develops and commercialises innovative medicines in areas of unmet medical need.
Your new role
Working in a team based in West London as a Clinical Trial Management Associate within HIV therapy area. This job would be ideal for an experienced Clinical Research Associate (CRA) or Senior Clinical Research Associate who wants to move into Study Management.
You'll have demonstrated proficiency in all relevant areas of Clinical Project Assistant as you'll provide administrative assistance in site selection, study implementation and ongoing coordination of study sites, either directly or via CROs. You'll also assist global trial managers with set-up of central labs and study vendors as required, including liaising with study management CRO to ensure site training and timely initiations.
You'll perform accompanied visits (PSSVs, SIVs, RMVs) with CRO CRAs to ensure correct study procedures according to SOPs and protocol procedures, and review of routine regulatory documents/files in compliance with protocol, regulatory requirements, SOPs, and Monitoring Plan, as required.
You'll review trip reports generated by CRO CRAs and communicate and collaborate with other functional groups to ensure efficient management of study activities. You'll also assist with the preparation and organisation of international investigator meetings, and in preparation of safety, interim and final study reports, including resolving data discrepancies.
You'll perform administrative duties in a timely manner as assigned. This job also requires up to 10% of travel.
What you'll need to succeed
A BS or BA in a relevant scientific discipline as well as relevant Clinical Trial experience in the pharmaceutical or health care industry or equivalent.
CRA experience is a must in this job role. You have the ability to engage and manage multiple stakeholders to achieve the objective, and are curios with learning agility. You'll need to be organised with systematic approach to prioritisation, and process oriented with critical thinking and excellent problem solving skills.
You need excellent verbal, written, interpersonal and presentation skills. You're also familiar with routine medical/scientific terminology, and Word, PowerPoint, and Excel.
Knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct if clinical trials is desirable. You're also able to participate in departmental or interdepartmental strategic initiative under general supervision.
What you'll get in return
- £COMPETITIVE salary
- Bonus & great pension scheme
- Excellent development & progress opportunities
- Dress down Fridays!
- Possibility to work home-based 1-2 days a week
- Flexi time
- Free fizzy drinks, and bagels on Wednesdays!
Please contact Anu Luur for more information about this job.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.
Hays Specialist Recruitment Limited
HVIVO Services Ltd
Osborne Clarke LLP