Senior Clinical Research Associate

This is a fully remote position, open to applicants in Turkey.

📋 Description

• You will oversee and manage the progress of clinical studies at investigative sites, ensuring that these studies are conducted, documented, and reported in accordance with the protocol, SOPs, ICH-GCP, and all relevant regulations and standards.

• You will coordinate all essential activities necessary for setting up and monitoring a study, such as identifying investigators, assisting in the preparation of regulatory submissions, and conducting pre-study and initiation visits.

• Senior CRAs are responsible for managing appropriately sized clinical trials and providing support to Project Managers on larger scale trials.

• You will have the chance to train and mentor junior staff members.

• You will engage directly with clients, initiate payments, and take part in proposal activities, including development and client presentations.

⛳️ Requirements

• A university degree in life sciences, pharmacy, or another health-related discipline, or equivalent experience in a scientific or healthcare field, or be a licensed healthcare professional.

• A minimum of 3.5 years as a CRA in a CRO, pharmaceutical, or biotech industry, or equivalent relevant experience and/or demonstrated competencies. Significant site management experience or equivalent experience in clinical research is required.

• Experience in oncology monitoring is essential.

🏝️ Benefits

• Excellent communication and organizational skills are crucial, along with being a team player.

• Demonstrated evidence of a client-focused approach.

• Proficiency in using computerized information systems, electronic spreadsheets, word processing, and electronic mail is required.

• Ability to travel overnight, with an average of up to 60% travel based on regional requirements. International travel may be necessary.

• Fluency in English and Turkish is required.