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Laboratory Study Co-Ordinator

Employer
Simbec-Orion
Location
Merthyr Tydfil, United Kingdom
Salary
Competitive
Start date
7 Jun 2022
Closing date
7 Jul 2022

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Discipline
R & D , Laboratory
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

ABOUT US

Simbec-Orion is a responsive and agile full-service CRO, with wide therapeutic experience and specialist expertise in clinical pharmacology, oncology and rare diseases. Perfectly structured, we provide full-service clinical development solutions for small and mid-size drug developers - headed up by a centralised leadership team.

With a focus on tailormade and scalable solutions, we'll adapt our delivery style, communications and operations to suit the demands of the project, helping clients achieve their clinical and commercial objectives. Because our goal is the same as theirs; to improve patients' lives.

THE JOB

We are looking for a Laboratory Study Co-Ordinator. You will be based in Merthyr Tydfil (Wales).

You will a ssist in the study management of clinical trial testing , work ing with other members of the study management and laboratory project management team and you will assist the Study Supervisor wherever possible to ensur e testing requirements have been accurately set up within the department LIMS system and that the necessary QC checks have been performed within the defined turn around times. You w ill also assist the Study Supervisor in the approval and release of L aboratory results when required .

KEY ACCOUNTABILITIES
  • Assist in the study set up of clinical studies within the Laborat o ry Services department.
  • Define testing requirements within the department LIMS (Lab Information Management Software) system .
  • Assi s t in the approval and release of Laboratory results for clinical studies.
  • Conduct QC checks on study - related documentation where required .
  • Ensure that work performed adheres to good practice regulations and guidelines.
  • D ocument procedures that are undertaken in a clear, accurate man ne r and apply Quality Control (QC) to ensure their accuracy.
  • Communicate the status of work being performed and escalate where appropriate to the Study Supervisor, Study Manager, P athology Laboratory M anager and Laboratory Project Manager.
  • Maintain personal training records, to demonstrate competency.

SKILLS REQUIRED

  • Science degree or equivalent.
  • High level of attention to detail
  • Excellent computer skills , including word processing and spreadsheet applications
  • Ability to work in line with standard operati ng procedures and working instructions
  • Ability to generate and maintain effective working relationships with team members and managers
  • Ability to work in a fast-paced environment
  • Strong interpersonal, communication, organisational and time management skills
  • Ability to handle multiple tasks at one given time.

WHY YOU SHOULD JOIN US

Simbec-Orion is growing fast. To keep up with demand, we're looking for the best people, from all areas of clinical development, to join our team.

We're dedicated to bringing the latest advances in science to market. Exposure to truly innovative new drugs in patient populations with serious unmet medical needs is what drives our company - and your reason to be a part of it.

With experts from all disciplines under the same roof, you'll work alongside some of the industry's best. So if you'd like to further your career within challenging therapeutic areas in rare disease, oncology, or at our clinical pharmacology site, or laboratory services. We're waiting to hear from you.

Simbec-Orion is an equal opportunity employer. Simbec-Orion will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law.

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