Study Coordinator - Cannock, United Kingdom - MAC Clinical Research

Tom O´Connor

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Tom O´Connor

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Description
MAC is a full-service global Contract Research Organisation (CRO). We also own a network of research sites. Our mission is to serve with honesty and integrity to make an outstanding contribution to human health.

We are seeking to appoint a Study Coordinator to join our dedicated team in Cannock.


The focus of this role is to effectively coordinate and carry out clinical research trials and procedures in accordance with ICH GCP, whilst gaining experience of more technically complex studies.


KEY SKILLS, KNOWLEDGE AND QUALIFICATIONS REQUIRED:

  • RGN/RMN, BSc Nursing _
    or_ BSc Biomedical Science or equivalent related field _(a psychology degree would be desirable)_
  • At least 1 year clinical trials experience

RESPONSIBILITIES:


Clinical Activities:

  • Perform primary coordinator role on specific clinical trials.
  • Perform the 'Lead Study Coordinator' role, to provide crosssite support and expertise
  • Assist the Clinical Science team with technical procedures where required
  • Carry out all clinical tasks efficiently and effectively and as per protocol.
  • To be the primary point of contact for specific study related queries.
  • Display sound organisational skills and the ability to prioritize own workload.
  • Review patient source notes in relation to study inclusion / exclusion criteria.
  • Effectively delegate study procedures to the clinical team.
  • Assist in the scheduling of patient visits as per protocol.
  • Set up and maintain all study related documentation including all site files.
  • Monitor and appropriately report AE's/SAE's.
  • Ensure that all patient visits are completed in accordance with the protocol.
  • Monitor clinical supplies and IMP and initiate resupply where required.
  • Develop clinical rating scale skills
  • Develop skills in prechecking of patient medical histories
  • To attend all study related meetings where requested.

Patient and Customer Care:

  • Welcome patients into the clinic and optimize patient experience.
  • Prioritize and promote patient safety.
  • Deal courteously and professionally with patients and customers at all times.
  • Ensure a pleasant and safe environment for all visitors to the clinic.
  • Ensure patients fully understand procedures and encourage them to express any concerns.
  • Communicate efficiently and professionally with the rest of the clinical team to ensure optimal patient care.
  • Deal with complaints in accordance with company policies

BENEFITS:


  • Competitive salary in keeping with pharmaceutical industry standards and will reflect experience
  • Health Insurance
  • Free onsite parking
  • 25 days annual leave (increasing in increments to 30 days after 6 years service)
  • Your birthday off work

Job Types:
Full-time, Permanent


Benefits:


  • Company pension
  • Free parking
  • Onsite parking
  • Private medical insurance

Schedule:

  • Monday to Friday

Ability to commute/relocate:

  • Cannock: reliably commute or plan to relocate before starting work (required)

Education:


  • Diploma of Higher Education (required)

Experience:

- line management: 1 year (preferred)
- clinical project management: 1 year (required)


Work Location:
One location

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