Randstad, as the EMEA Johnson & Johnson talent acquisition partner, is responsible for finding and contracting talent for the contingent roles at Johnson & Johnson. If you are selected for a role you will be engaged or employed by one of the Randstad recruitment companies in EMEA and will not be an employee of Johnson & Johnson.

Johnson & Johnson

Senior Clinical Trial Leader - remote role

Posted Aug 16, 2022
Job ID: JJJP00011969
Location
Leeds, Remote
Hours/week
37 hrs/week
Payrate range
24 - 26 £/hr

Senior Clinical Trial Leader - remote role

(Ethicon - part of the Johnson & Johnson Medical Devices Companies)

12 month contract to start ASAP

This role can be done remotely but you must be in the UK and you must already hold the right to work in the UK

The company:

Ethicon has made significant contributions to surgery for more than 100 years, from creating the first sutures, to revolutionizing surgery with minimally invasive procedures.

Our surgical technologies and solutions include sutures, staplers, energy devices, trocars and hemostats along with interventional ablation, robotic and digital solutions. 

At Ethicon, our goal is better outcomes for everyone, everywhere.

The Role:

This individual will be responsible for leading one or more clinical trials within the R&D Clinical Operations group, as well as fostering strong, productive relationships with colleagues across the organization. You will serve as the trial leader for clinical study execution.

Key Responsibilities:

Serves as a Senior Clinical Trial Leader within the R&D Clinical Operations group to execute company sponsored clinical trials for the Ethicon Medical Device Franchise 
 

Manages all operational activities of assigned clinical studies within the R&D Clinical Operations group  

 

Serves as a member of the clinical trial/study core team, and serves as the liaison with R&D Clinical Franchise and R&D Clinical Biometrics for assigned clinical trials 
 

Provides 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 
 

Is accountable for quality, compliance with regulations and company procedures, timelines, and budgets for assigned clinical trials


Solves problems with support from Clinical Management arising during clinical study execution, and will seek guidance for more complex problems, as needed 


Supports the development/implementation of new clinical systems/processes, and provides support for cross sector clinical operations initiatives, as needed 

Interfaces and collaborate with site personnel, IRBs/ECs, Competent Authorities/MoH, contractors/vendors, and company personnel 
 

Ensures efficient use of resources within the clinical study/program to provide high quality deliverables


Provides direction to and oversight of Clinical Research Associates/Site Monitors, as it relates to clinical trial conduct


May provide direct oversight of CRO(s) or other vendors as needed for assigned clinical trials


May serve as the primary contact for clinical trial sites 


May review and provide feedback on clinical operation section of protocols 


May be involved in other tasks to support R&D Clinical Operations and R&D Clinical Franchise as needed 


Ensures that all Human Resource related activities, and decisions embody the Johnson & Johnson Credo Values


 

Qualifications required:

Education:

Bachelor’s degree or equivalent required, preferably in Life Sciences (e.g. Biology, Chemistry, Biochemistry, Nursing, Pharmacy).

 

Experience and Skills:

Required:

Minimum of 4 years of clinical research experience acquired in medical device or pharmaceutical industry, CRO or investigational site.


Previous experience in clinical trial management or equivalent


Understanding and application of Good Clinical Practices


 

Preferred:

Relevant industry certifications (i.e., CCRA, RAC, CDE).

Clinical/medical background

Medical device experience


Other:

This position may require some travel, primarily for meetings.


In Return:

In return for this role you will receive a very competitive hourly rate. A minimum 12 month contract & an opportunity to work with a Global Leader within the Pharmaceutical sector, Johnson & Johnson. 

 

Things to remember before applying for this role:

  • We are looking to process the first round of applications within the next 1-2 working days.
  • We do not accept applications via email.


 

If you are interested in this role please apply now! Make sure you fill out your application in full, your personal CV will be used for the recruiter’s reference only, they are not sent to Hiring Managers. Ensure all relevant information is included in your application! 
 

Thank you very much and we look forward to receiving your application. 
 

If you would like some additional information about the role please contact: Trish.Delaney@randstadsourceright.co.uk


 

Diversity, Equity & Inclusion:

 

For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.

 

We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences

That is why we are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential. No matter who they are. Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”.


 



 

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