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Clinical Data Coordinator
2 weeks ago
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 Data Coordinator to join our very busy, dedicated team at our Liverpool site.
The focus of this role is to provide comprehensive data handling support and facilitate with the smooth running of MAC Clinical Research team activities, along with some reception cover when required.
This is an extremely busy department, and this role would best suit someone who enjoys a fast-paced working environment, has an eye for accuracy and detail, a strong work ethic and previous reception experience.
KEY SKILLS, KNOWLEDGE AND QUALIFICATIONS REQUIRED:
- Knowledge and experience in administration, data entry and QC auditing.
- Previous background of working in healthcare setting (NHS, GP, Dentistry or Pharmacy)
- Previous experience of working on reception
- Some understanding of medical terms/terminology
- An ability to easily pick up new data management systems
RESPONSIBILITIES:
- Responsible for ensuring that clinical trial data across multiple studies is accurate, complete and in line with ICH GCP and ALCOAC principles
- Responsible for ensuring the accuracy of completed clinical trial documents, inclusive but not exhaustive of; essential documents with the ISF, clinical source documents and completed informed consent forms
- Present a positive image as a representative of MAC Clinical Research with sponsors
- Interact with external vendors in order to accommodate receipt of essential source data files/records (central labs, imaging vendors etc.) and ensure internal medic review is completed in timely manner
- Transcribe from paperwork to data base and alert the team in any identified discrepancies with data
- Attend investigator Meetings and disseminate role specific learnings across all UK sites as required
- Utilise company management system, Envision, to upload source documents as required
- Collaborate with CRAs/internal/external auditors and Site Directors to ensure protocol deviations are appropriately managed, documented and communicated
- Data quality, receptionist cover when needed, multiple methods of communication, planning and organising.
- Seek opportunities for self-development
- Patient confidentiality and GDPR adherence
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
- Free parking
- Health & wellbeing programme
- On-site parking
- Private medical insurance
- Referral programme
Schedule:
- Monday to Friday
Application question(s):
- Do you require sponsorship to work in the UK? (Now or in the future)
- Are you aware that the role is fulltime and based onsite at our clinic in Merseyside?
**Education**:
- GCSE or equivalent (required)
Work authorisation:
- United Kingdom (required)
Work Location: In person
