Non-Monitoring Snr Clinical Research Associate for Leadershi

Leadership and Management Focused, Non-Monitoring Senior Clinical Research Associate
Contact Information:

Lee Dunn
Tel: +44 (0) 207 255 6665
[Email hidden]
http://www.1st-pharmapeople.com

Job Summary:

In this position you will only be required to monitor on a short term basis to fill in gaps based on holiday and sickness. As a Principle/Lead Clinical Research Associate discounting the monitoring of study timelines, patient recruitment and budget, you will be responsible for managing clinical monitoring activities and liaising with project management and the sponsor (If appropriate) to ensure that the clinical deliverables are met. This is done in a fully home based capacity for a very large and successful CRO

Offers:

The role offers a negotiable salary based and benefit package on your experience and situation. Benefits will typically include: Car allowance, 25 days holiday, Pension, BUPA, insurance and personal development schemes. A specific emphasis is placed on organic growth so career opportunities are always available or clearly outlined in this case Clinical Project Management would be the next most logical and easiest step. Flexi-time is also available as is a multitude of projects with some of the largest and most prestigious companies in the industry.

Candidates:

Thorough knowledge of ICH and UK regulatory authority regulations regarding drug research and development are essential for this role. As is also substantial clinical research experience; including a minimum of 2-3 years monitoring experience and managing investigative clinical trial sites.
Experience of leading professional staff in a clinical research environment alongside having an undergraduate degree in a clinical, scientific, or related field or its international equivalent, or equivalent work experience required

Responsibilities:

The main responsibilities of the Clinical Lead are: Directing a project team; Early recognition of areas of potential problems and formulate contingency plans; Evaluating and identifying resourcing needs and provide performance feedback as appropriate; Organizing and participating in client, investigator and team meetings; Identifying and facilitating study training needs; Review of visit reports; Monitoring study timelines and patient recruitment to ensure successful outcome of the project; May be required to monitor site(s) as per client or project request; Maintaining and assuring quality of work generated; Continually monitoring budget to ensure project milestones and budget are achieved; Identifying changes in scope and liaising with Project Manager; Compiling monthly reports in a timely manner; Proactively ensuring that all invoicing is completed in a timely manner; Effectively communicating with internal and external customers as well as third party vendors.

If you are interested and believe you are qualified for this role then please send you most recent CV/Resume along with a summary of why you feel you would be ideal based on the responsibilities above.

If you would to discuss this role in greater detail or your application / suitability to this or further roles, please call me or email me in confidence. If you are not available or suited to this position, please feel free to pass my details on.

This company is acting as an Agency and/or Employment Business

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