Clinical Trial Monitor - Senior

ProClinical Ltd
High Wycombe
09 Mar 2018
15 Mar 2018
Contract Type
Full Time
Here is a chance to join one of the most globally known pharmaceutical organisations, who is looking to hire a Clinical Trial Monitor based in High Wycombe. This job will be working a top 10 pharmaceutical company that works across a range of industries from medical devices to pharmaceutical and consumer goods, operating in over 60 countries.

This individual will be responsible for clinical project management within the company's franchise, as well as fostering strong, productive relationships with colleagues within the organization. Serves as a member of the study core team and may serve as the liaison with the operating company for projects under his/her responsibility.

Job Responsibilities:

* Ensure that all Human Resource related activities and decisions embody the company's Values.
* Provide leadership within a clinical study, ensuring that each Team Member has a well-defined set of activities and objectives specific to their role and responsibilities within the context of their business focus.
* Ensure efficient use of resources within the clinical study to provide high quality deliverables. Business Leadership
* Accountable for quality, compliance with regulations and company procedures, timelines, and budgets for assigned clinical projects.
* May lead several small/medium clinical studies (regulated and non-regulated) and/or a small number of large non-regulated projects that may involve Clinical Research Associates (CRAs) and/or other clinical operations staff (i.e., ?250K USD annual investment).
* May assist with the management of large regulated studies under supervision of CPM or Senior CPM.
* May support CPM and/or Senior CPM within a large or complex clinical study.
* Identify and ensure strategies, resources, and accountabilities are in place to achieve rapid, high quality execution of assigned clinical studies under his/her responsibilities.
* Independently solve simple problems arising during clinical study execution, guidance required for move complex problem solving.
* Manage all activities of assigned clinical studies within the Franchise Clinical Operations department.

Skills and Requirements:

* Minimum of a bachelor's Degree, preferably in a Life Science, Physical Science, Nursing, or Biological Science.
* BS with at least 3 years of relevant experience preferred.
* Previous experience in clinical study management or equivalent is required. Relevant industry certifications preferred (i.e., CCRA, RAC, CDE).
* Clinical/medical background a plus.
* Medical device experience a plus. Knowledge
* Requires basic skills in project management
* Requires understanding of Good Clinical Practices.
* Understanding and application of regulations and standards applied in clinical areas is required.
* Written and verbal communications
* Presentation and influencing
* Organizational skills
* Ability to travel up to 50%.

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 call Chantelle Perrault on Phone number removed or upload your CV on our website - URL removed
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.

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