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Job Details

CTM - Study Manager (Pharma Dedicated) - UK-128525

Company: PPD
Location: Europe, Middle East & Africa-UK-England-Uxbridge
Reference: 128525
Closing Date: 09 Dec 16
Type: Full Time
Salary (£): On Application
Benefits:

Job Summary:

PPD has an exciting opportunity for a Clinical Team Manager (CTM/Study Manager) to join exclusively for one of our strategic pharmaceutical partners in Uxbridge, West London.  PPD works in collaboration with this partner; you will be dedicated to the client projects and sites, working within their teams, systems and processes on behalf of PPD. ...

Requirements:

PPD has an exciting opportunity for a Clinical Team Manager (CTM/Study Manager) to join exclusively for one of our strategic pharmaceutical partners in Uxbridge, West London.  PPD works in collaboration with this partner; you will be dedicated to the client projects and sites, working within their teams, systems and processes on behalf of 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 industry who would enjoy the opportunity to work for a CRO dedicated to one client.     The role coordinates all aspects of clinical activities on an national basis.  Responsible  for the local implementation of international clinical trials and / or local trials entrusted to them, their preparation for their closure, in compliance with GCP, regulatory requirements, SOPs, quality standards, deadlines and budgets.   This could co-ordination of the Clinical Research Associates who are allocated to a project on a Country basis. 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, and be primarily responsible for the clinical deliverables of the Project within agreed timelines and budget.   We are seeking high performing individuals who enjoy a fast-paced environment and have had Clinical Management experience OR exposure to local studies, involving the coordination of CRAs locally and potentially across different countries. 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 countries. 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.   We are seeking highly motivated and skilled applicants who will want to share in our continued growth in the international market place. We will consider field based applicants depending on your experience level.   PPD is a leading global contract research organization providing drug discovery, development, lifecycle management, laboratory services and outsourcing solutions.   With offices in 46 countries and more than 15,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a commitment to quality to help clients and partners accelerate the delivery of safe, effective therapeutics to patients and maximize returns on their R&D investments. *LI-JP1  

Qualifications

 

Education and 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.
  Knowledge, Skills and Abilities:
  • 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

*LI-JP1

       

Apply for this job: CTM - Study Manager (Pharma Dedicated) - UK-128525

Contact Information:

Address:  PPD Cambridge
Granta Park
Great Abington
Cambridge

CB21 6GQ
England
Tel:  +44 1223 374100
Website:  Visit Our Web Site

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