CTA

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 minimal 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.

If you are having difficulty in applying or if you have any questions, please contact Matthew Pike at +44 207 4400 639 or m.pike@proclinical.com.

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.

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