Clinical Trial Assistant

5 months ago

Prescot, United Kingdom MAC Clinical Research Full time

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 Clinical Trial Assistant to join our dedicated team in Merseyside.

Please note this is an on-site role based in Merseyside. There will be some flexibility needed to work nights/weekends when required.

FOCUS OF THE JOB:

- To prioritise patient safety by ensuring adherence to ICH-GCP
- To carry out clinical trial procedures in accordance with ICH-GCP

KEY SKILLS, KNOWLEDGE AND QUALIFICATIONS REQUIRED
- BSc in a scientific field

RESPONSIBILITIES
- Ensure that all patient visits are completed in accordance with the protocol.
- Monitor clinical supplies and initiate resupply where required.
- Welcome patients into the clinic and optimize patient experience, prioritising and promoting 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.
- Assist the study co-ordinator in the set-up of the laboratory files in preparation for study commencement.
- Assist with completion and updating of laboratory files and logs.
- Assist with laboratory procedures including, sample processing and packing (appropriate training and IATA certification required).
- Where delegated, ensure the monitoring and supply of study specific blood kits.
- Dispense medications via study specific method e.g IVRS/IWRS.
- Assist in the maintenance of all study related documentation including Investigator Site File (ISF), Pharmacy file (IPH), and patient documentation in accordance with ICH-GCP.
- Ensure meticulous recording and transcription of data in both clinical and research notes.
- To work to the requirements of SI 2004 no 1031 and amendments thereof, which includes Good Clinical Practice
- To work according to MAC SOPs, guidelines and policies
- To work according to current data protection standards and practice good information management. Maintenance of strict confidentiality of patient and business related data.

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

Pay: £24,000.00 per year

**Benefits**:

- Company pension
- Cycle to work scheme
- Free parking
- Health & wellbeing programme
- On-site parking
- Referral programme
- Sick pay

Schedule:

- Monday to Friday
- Night shift
- Weekend availability

Application question(s):

- Do you require sponsorship to work in the UK? (Now or in the future)

**Education**:

- Bachelor's (preferred)

Work authorisation:

- United Kingdom (required)

Work Location: In person

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