clinical trial manager in leeds

posted
job type
contract
salary
£ 55,000 per year
apply now

job details

posted
location
leeds, yorkshire and the humber
job category
pharmaceutical
job type
contract
working hours
Full-Time
salary
£ 55,000 per year
reference number
CLCT
apply now

job description

Are you an experienced Clinical Trials Manager? Are you looking to take on a new challenge with a Medical Devices Manufacturer? If so we are looking for individuals just like you!

We have an opportunity for a Clinical Trials Manager to join a leading client of ours. This is a contract opportunity for 6 months initially, working 40 hours per week Mon-Fri.

Benefits;



* Free on-site gym
* Free on-site parking
* On-site restaurant
* Weekly pay
* Pension contributions

Responsibilities:



* Serve as a Clinical Trial Leader within Clinical & Medical Strategic Operations to execute company sponsored clinical trials
* Manage all operational activities of assigned clinical studies
* Serves as a member of the clinical trial/study/program core team and may serve as the liaison with the Clinical Franchise and Clinical BSDM for projects under his/her responsibility
* May serve as the primary contact for clinical trial sites
* Can independently solve problems arising during clinical study execution, and will seek guidance for more complex problems, as needed
* Provide internal communication of important clinical data and events. Functions as a reliable, trusted resource of accurate, up-to-date project knowledge as requested by key stakeholders
* May be involved in other tasks to support Clinical & Medical Strategic Operations and Clinical Franchise as needed
* Track and manage assigned clinical trials/programs budgets to ensure adherence to business plans
* Support the implementation of new clinical systems/processes, as needed.
* Interface and collaborate with site personnel, IRBs/ECs, Competent Authorities/MoH, contractors/vendors, and company personnel
* Ensure personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety, and
* Environmental compliance
* Manage resources assigned to designated clinical studies to provide quality deliverables while maintaining optimal efficiency

Qualifications/Experience



* Minimum of a Bachelor's Degree preferably in Life Science, Physical Science, Nursing, or Biological Science required
* BS with at least 6 years experience, MS with at least 5 years experience, PhD with at least 3 years of relevant experience
* Previous experience in clinical trial management is required
* Experience working well with cross-functional teams is required
* Clinical/medical background a plus
* Medical device experience a plus

If this role is of interest to yourself, and matches your skills sets and experience then please click apply below to submit your CV. Please ensure your up to date contact details are on your CV before applying. If your application is shortlisted, we will call you and discuss the role in further detail to ensure this role is what you are looking for and meets our client's needs.

Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.

Candidates must be eligible to live and work in the UK.

For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business.