Study Coordinator - Blackpool, United Kingdom - MAC Clinical Research
Description
Focus of the Role
- Gain experience of the clinical trial process and become proficient in all aspects of clinical trial coordination
- To carry out clinical trial procedures in accordance with ICH GCP
KEY SKILLS, KNOWLEDGE AND QUALIFICATIONS REQUIRED
- Familiar with clinical/scientific document completion, organising paperwork and filing (essential)
- Ability to effectively communicate at all levels (essential)
- A great team player with an ability to work independently when required
RESPONSIBILITIES:
- Data management
- Patient and customer care
- Clinical activities
- Laboratory
- Pharmacy
PHYSICAL, WORK ENVIRONMENT, TRAVEL DEMANDS:
- Potentially long periods standing.
- Dealing with bodily fluids.
- Long periods looking at a computer screen.
- Meeting deadlines and working within strict timelines.
- Ability to travel between sites if required.
- Ability to travel to national / international meetings.
BENEFITS:
- Competitive salary in keeping with pharmaceutical industry standards that 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
Benefits:
- Company pension
- Private medical insurance
- Work from home
Schedule:
- 8 hour shift
Work authorisation:
- United Kingdom (required)
Work Location:
In person
Reference ID:
HR286
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