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Screening Supervisor

Employer
Labcorp
Location
Leeds, United Kingdom
Salary
Competitive
Start date
22 Sep 2020
Closing date
22 Oct 2020

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Discipline
Clinical Research, Clinical Operations
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details


Permanent position available to join our Phase I Clinical Research Unit in Leeds, West Yorkshire, as aSupervisor - Screening. This is a unique opportunity to gain experience within Clinical research/trials and allow you to continue to practice your leadership skills.

COVANCE is a leading global drug development services company providing support to the Pharmaceutical and Biotechnology industries. At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career. This is your chance to become part of a team that helps to bring the miracles of medicine to market sooner.

About the Role

Your main duties will include, but not be restricted to:
  • Directly supervise and work alongside staff, demonstrate ability to lead by example and to encourage team members to seek solutions.
  • Instill in all team members responsible to him/her the Company's commitment to quality and meeting the client's requirement without error, on time, every time.
  • Ensure that that the staff under his/her supervision area is adequate in quality and quantity to meet agreed forecasted workload. Recommend changes if necessary and justify them in accordance with company policy.
  • Coaches and mentors staff. Initiates, plans and implements appropriate staff development programs.
  • Perform supervisory duties including but not limited to interviewing, hiring, training, intervention, discipline, and discharge of screening staff.
  • Responsible for ensuring that the screening of the volunteers at the site is conducted to the highest possible quality and in accordance with the protocol, SOPs, and ICH/GCP guidelines.
  • Schedules investigators for protocol-related tasks.
  • Manage his/her area so as to meet the budgeted standard of performance.
  • Updates or creates SOPs/P&Ps/EOPs germane to their area of expertise.
  • Ensure that screening procedures comply with all regulatory requirements and guidelines and that the highest ethical standards are maintained at all times. In particular, ensure proper records are maintained and that these meet all applicable regulatory requirements.
  • Monitor and assess response to scheduled screening appointments to adequately meet the requirements of the protocol.
  • Respond constructively to supervisor and QA ensuring that any GCP/ICH deficiencies are followed up with prompt remedial action.
  • Responsible for tracking screening activities on all enrolling protocols at the site.
  • Maintain relationship with participants through phone calls, emails and face to face interaction at the site.
  • Attends scheduling meetings, site initiation meetings and ad hoc meetings to discuss upcoming studies.
  • Manage subject complaints by proactively resolving issues as they arise.
  • Manage post screening data process and selection of panels for eligible and standby subjects for specific studies
  • Ensure that all necessary screening tasks have been performed including height, weight, frame size, venepuncture, vital signs, electrocardiograms, spirometry and simple laboratory procedures as needed and required per the study protocol. Must be competent to perform these tasks when needed.
  • Produce screening reports-analyzing the data to ensure efficient running of the screening department.

We Offer the opportunity to work within an experienced and highly skilled team and together with Covance's ongoing success offer you the prospect of unsurpassed growth and career development opportunities.

Covance offers a comprehensive benefits package including:
  • Competitive salary
  • Life Assurance
  • Pension
  • Private
  • Health Insurance
  • Other voluntary opt-in benefits including Dental insurance, health screenings and many others

Get ready to redefine what's possible and discover your extraordinary potential at Covance. Here, you'll have the opportunity to personally advance healthcare and make a difference in peoples' lives with your bold ideas and unique point of view. With the support of exceptional people from across the globe and an energized purpose, you'll be empowered to own your career journey with mentoring, training and personalized development planning.Join us as we speed the delivery of ground breaking therapies and anticipate tomorrow's drug development challenges, creating new possibilities for our clients-and your career.
Education/Qualifications:
  • B.A. or B.S. in Communication, Health Administration, or other related field
Experience:
  • Recent and relevant experience
  • Experience in a medical field would be preferrable
  • Additional experience may be substituted for education requirements

Company

At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions —because we know that knowledge has the potential to make life better for all. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives. Join us in our pursuit of answers.

 

 

 

 

Company info
Website
Location
Maidenhead Office Park
Westacott Way
Littlewick Green
Maidenhead
SL6 3QH
United Kingdom

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