CRA- SCRA, Turkey

Proclinical are partnering with a CRO who are currently recruiting or an individual to join their team. This role is on a permanent basis with the ability to work remotely from anywhere in Turkey. The opening position available is for a CRA-SCRA.

Responsibilities:

• Operate on arranging actions to set up and supervise a study, finishing precise study reports and upholding study documentation.
• Propose protocol, consent documents for ethics/IRB approval and support in preparing regulatory proposals as requested.
• Contribute to preparing and evaluating documentation and feasibility studies for new submissions as necessary.
• You will balance sponsor produced questions effectively and be accountable for study cost-efficiency.
• The ideal candidate might coach and mentor less experiences CRAs and/or lead CRAs working on global projects depending on own experience.
• Other duties may be assigned to this role.

Key Skills and Requirements:

• Demonstrable experience in monitoring phase I - III trials in a CRA role.
• Expertise on ICG GCP regulations and knowledge of evaluating medical data.
• Communication skills both verbally and in writing.
• Fluency in the English language.
• Capable of creating precise work to meet tight deadlines in a pressurised setting.
• Willing to travel for business needs up to 60% of the time with a valid driver's license.

If you are having difficulty in applying or if you have any questions, please contact Carlos Rios at +44 203 148 8352.

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.

#Clinical