Skip to main content
Post your CV and find your next job on Indeed!

Clinical Trials jobs in Wigan West

Sort by: -
    • Accelerating clinical breakthrough for our customers, our patients, and for future generations.
    • Panthera is an independent Site Management Organisation helping…
  • View similar jobs with this employer
    • A DBS check is a background check that reveals any criminal convictions, cautions, reprimands, or warnings.
    • The level of check required depends on the role:
    • You will need a health service background, knowledge and experience of research, clinical trials coordination, delivery and monitoring, and experience obtaining…
    • With experience working in academic clinical trials or clinical research within the NHS.
    • Advise and negotiate on clinical trial agreements including financial…
    • To have full oversight of clinical trial submission process within teams and overall responsibility from feasibility through to closing out of a team portfolio…
  • View similar jobs with this employer
    • Provision of medical care and oversight of clinical trial participants.
    • Assist clinical staff members in various clinical activities as required.
  • View similar jobs with this employer
    • Provision of medical care and oversight of clinical trial participants.
    • Assist clinical staff members in various clinical activities as required.
    • Collaboration with experienced clinical and operational professionals.
    • Coordinating project delivery across clinical and operational teams.
    • Coordinating clinical project delivery, from initiation through to closure.
    • Understanding of healthcare operations, clinical workflows or NHS systems.
    • Exposure to clinical trial or quality improvement projects.
    • Coordinating clinical project delivery, from initiation through to completion.
    • § To liaise with the stakeholders and other project representatives to determine precise requirements in terms of specification and other clinical or user-based…
  • View similar jobs with this employer
    • Participate in clinical trial feasibilities and risk assessments of clinical trial protocols.
    • Arrange and facilitate clinical trial related meetings.
    • Contract: Fixed-term contract until 31st August 2028, full time (35 hours per week).
    • Join LSTM as our Market Access and Commercialisation Manager and play a key…
    • Experience contributing to publications, grant development, collaborative projects or research activity with clinical, industry or international partners.
    • Experience in pharmacoepidemiology or related clinical research areas.
    • Manage day-to-day delivery of the MERMAID project, coordinating activities, tracking…

Job Post Details

Study Coordinator - job post

Panthera Biopartners
4.0 out of 5 stars
228 Garstang Road, Preston PR2 9QB
£25,725 - £28,350 a year - Permanent, Full-time
Responded to 75% or more applications in the past 30 days, typically within 3 days.

Job details

Pay

  • £25,725 - £28,350 a year

Job type

  • Permanent
  • Full-time

Location

228 Garstang Road, Preston PR2 9QB

Benefits

Pulled from the full job description

  • Annual leave
  • Life insurance

Full job description

Patient Study Coordinator - Preston

An exciting opportunity has arisen due to growth, for a Patient Study Coordinator to join our Preston Clinical Research Site

Panthera is an independent Site Management Organisation helping pharmaceutical and contract research organisations find the right patient, for the right trial, at the right time. The Panthera team is run by a world-class team of experts with more than a hundred years of clinical research experience.

We put the patient at the heart of everything we do to ensure the best experience and environment for volunteers and participants. Accelerating clinical breakthrough for our customers, our patients, and for future generations.

Job Summary

The Patient Study Coordinator will be responsible for the day-to-day coordination and administration of the Clinical Research Site, ensuring the filing system are maintained for patient notes and the clinic notes are ready for the next day’s clinic; as well as supporting the Site Manager with services coordination such as vendor management, purchasing, quality systems management, diary management and administration.

The Patient Study Coordinator is responsible for ensuring that the Clinical Research Site is a welcoming environment for our patients, ensuring they are always treated with dignity, privacy and safety as our number one priority.

There may be a requirement to work across local Panthera sites as required from time to time.

Ideal Candidate

  • Excellent interpersonal skills, friendly and approachable
  • Pro-active and enthusiastic to ensure that high quality support and patient care is provided.
  • Evidence of experience working in a similar environment.
  • Previous experience in the healthcare sector is desirable but not essential.

Salary & Benefits Package

  • £25,725 - £28,350 per annum
  • 25 days annual leave plus bank holidays
  • Life insurance, 3x annual salary
  • Employee healthcare cash plan programme
  • Employee Assistant Programme
  • Enhanced sickness and family friendly policies

Panthera Biopartners provided the following inclusive hiring information:

We are an equal opportunity employer and consider all qualified applicants equally without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, veteran status or disability status.

INDHP

Job Types: Full-time, Permanent

Pay: £25,725.00-£28,350.00 per year

Ability to commute/relocate:

  • Preston PR2 9QB: reliably commute or plan to relocate before starting work (preferred)

Application question(s):

  • What is your current notice period?
  • Will you now or in the future require sponsorship for employment visa status?
  • What are your salary expectations?

Work authorisation:

  • United Kingdom (required)

Work Location: In person

Let Employers Find YouUpload Your Resume