Clinical Study Management Associate

£0.00 - £55000.00 per annum
  1. Permanent
  2. Project/Study Manager (CSM/CPM)
  3. United Kingdom
Surrey
Posting date: 07 Aug 2019
CR.MP.24709_1565188635

A historic pharmaceutical company is seeking to recruit a Clinical Study Management Associate to their office in Surrey. The organisation creates informative and engaging online communities that share information in meaningful ways. This vacancy offers an exciting opportunity to work with a leading and innovative pharmaceutical organisation that develops high quality medicines that meet real needs.

Job Responsibilities:

  • Act as the primary point of contact for institutions to identify and proactively resolve business process barriers.
  • Partner with other functional partners and vendors interacting with the sites and serving as the single point of accountability for the site (site selection, site activation, enrolment, data delivery, issue management, and closeout).
  • Influence the development and implementation of site initiation/enrolment risk plans for clinical trials to ensure delivery on enrolment commitments.
  • Own the issues management process at the site level, collaborating with company partners, Quality, and other team members through both formal and informal interactions to resolve/escalate site specific issues when necessary.
  • Oversee the delivery of data and clinical trial milestones at the site level.
  • Leverage strategic knowledge of institution's decision-making process along with historical performance with other company clinical trials to deliver mutually acceptable business solutions.
  • Influence the design of clinical study protocols including input to study manager on protocol and enrolment feasibility for studies to enable the successful enrolment and implementation of the clinical trial.
  • Maintain technical expertise within a therapeutic area to engage in scientism discussions with the investigator and institution personnel.
  • Develop and maintain relationships with therapeutic clinical trial sites.
  • If applicable, negotiate budgets and contracts with institutions and investigators with an emphasis on usage of standard agreements and Fair Market Value (FMV).

Skills and Requirements:

  • Demonstrable experience and education in a similar or related capacity.
  • Demonstrable multitasking, project management, and execution skills.
  • Good interpersonal skills, including communication, presentation, persuasion, and influence.
  • Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
  • Proficiency with computer skills, such as MS Office.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please contact Matthew Pike at +44 207 440 0639 or upload your CV on our website - www.proclinical.com.

A full job description is available on request.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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