Cta
2 weeks ago
Proclinical are recruiting a CTA for a small biotech. This role is on a permanent basis with the ability to work remotely from anywhere in the UK.
**Responsibilities**:
- Uphold study spreadsheets when needed to enable tracking/documentation of study status.
- Archive trial linked documents and keep the filing area organised and always inspection ready.
- You will schedule and attend internal study calls and take minutes/action items when required.
- Responsible for attending study team meetings in person.
- Participate in the development and evaluation of study documents.
- Support the development of study/program specific ISF and any other linked documents.
- Discover and approach new vendors based on study set up and needs.
- Other duties may be assigned to this role.
**Key Skills and Requirements**:
- At least 3+ years of experience within a similar position assisting the study team.
- Familiarity and comprehension of global trial set up.
- Comprehension of various phases of the trial, preferably from study initiation to closeout.
- Works well independently under mínimal supervision.
- Communication skills both verbally and in writing.
- Works well with others.
- Takes the initiative with a can-do mindset.
- A creative individual with the ability to think ahead.
- A fast learner with a high attention to detail.
- Educated to a degree level.
- Expertise on ICH GCP.
- Computer literacy.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
LI-MP1
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