Clinical Trial Manager/Clinical Study Manager

Clinical Trial Manager/Clinical Study Manager

PPD - Pharmaceutical Product Development

West London, United Kingdom

PPD has an exciting opportunity for a Clinical Trial Manager/Study Manager to join us dedicated to one of our strategic pharmaceutical partners in Uxbridge, West London, on a maternity cover contract. PPD works in collaboration with this partner; you will be dedicated to UK clinical projects, working with PPD’s successful study management team who are dedicated and on onsite with this large pharmaceutical company. You will be working to their systems and processes with the full support and development from PPD.

This is a great opportunity for CTM’s or Study Managers or those with relative experience working within the life science sector for pharmaceutical, biotech companies or CRO’s who would enjoy hand on clinical oversight, co-ordinations and study management.

The role coordinates all aspects of clinical activities for the UK trials for this pharmaceutical organisation. You will be responsible for the local implementation of international clinical trials and/or local trials entrusted to them, from start-up activities though to preparation for their closure, in compliance with GCP, regulatory requirements, SOPs, quality standards, deadlines and budgets.

You will work in partnership with the project teams to ensure the necessary training, tracking and quality systems are in place for the clinical team, primarily responsible for the clinical deliverables of the Project within agreed timelines and budget. This includes co-ordination of the Clinical Research Associates who are also allocated to UK projects working for PPD, dedicated to our sponsor.

We are seeking high performing and highly motivated individuals who enjoy a fast-paced environment and have study management experience involving the coordination of CRA’s. With your excellent written and oral English skills you will have exceptional interpersonal and problem solving skills, with the ability to lead CRAs in different based throughout the UK. You will also have proficient working knowledge of GCP and experience in several medical/therapeutic areas. You must be comfortable working in a matrix management system and have the ability to motivate, mentor and integrate teams.

EXPERIENCE:

  • Bachelor's degree or licenced certified health care training or equivalent combination of education and experience;
  • Clinical research experience in all phases of study life cycle, including start up, interim and close out;
  • Equivalent combination of education, training, and experience that provides the individual with the required knowledge, skills, and abilities;
  • Valid Driver's Licence;
  • Valid Passport;
  • Superior organizational skills;
  • Demonstrated performance management abilities;
  • Extensive monitoring experience;
  • Excellent judgment and decision making skills;
  • Effective oral and written communication skills;
  • Excellent interpersonal skills and problem solving ability;
  • Ability to motivate and integrate teams and teach/mentor team members;
  • Able to effectively prioritize workload;
  • Strong attention to detail;
  • knowledge of relevant regulations e.g. ICH/GCP, FDA guidelines, etc.

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© EuroJobsites 2019

EuroJobsites is a UK registered company number: 4694396 VAT number: GB 880 9055 04

Registered address: EuroJobsites Ltd, Unit 8, Kingsmill Business Park, Kingston Upon Thames, London, KT1 3GZ, United Kingdom

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