Clinical Research Associate

Chiron Medical CRO; Fatih; On-site; TRY 30,000 - 70,000; Full time

Job summary

An established industry player in clinical research is seeking a passionate Clinical Research Associate to join their innovative team in Istanbul. This role offers the chance to contribute to groundbreaking medical research and ensure the highest standards in clinical trials. You will be responsible for conducting site visits, verifying data integrity, and collaborating with trial sites to ensure compliance with protocols and regulations. If you are eager to make a difference in healthcare and thrive in a dynamic environment, this opportunity is perfect for you. Join a company that values diversity and is committed to excellence in clinical research.

Qualifications

• 2+ years of experience as a Clinical Research Associate.
• Strong understanding of GCP and ICH guidelines.

Responsibilities

• Conduct site initiation, monitoring, and close-out visits.
• Collaborate with clinical trial sites to ensure compliance.

Skills

GCP (Good Clinical Practice)

Organizational Skills

Communication Skills

Team Collaboration

Education

Bachelor's degree in a scientific or healthcare-related field

Tools

Microsoft Office

Job description

Subject: Job Opportunity: Clinical Research Associate at Chiron Medical CRO - Istanbul, Turkiye

Dear Candidates,

Chiron Medical CRO is a leading Contract Research Organization dedicated to advancing healthcare through innovative clinical research solutions in Turkiye. We are currently seeking a highly motivated and skilled Clinical Research Associate to join our dynamic team in Istanbul, Turkiye. If you are passionate about contributing to cutting-edge medical research and ensuring the highest standards of clinical trials, we invite you to apply for this exciting opportunity.

Position: Clinical Research Associate Location: Istanbul, Turkiye

About Chiron Medical CRO: Chiron Medical CRO is committed to excellence in clinical research, providing comprehensive services to pharmaceutical, biotechnology, and medical device companies. Our mission is to accelerate the development of life-changing therapies by conducting efficient and high-quality clinical trials.

Key Responsibilities:

1. Conduct site initiation, monitoring, and close-out visits in accordance with protocol requirements, regulatory guidelines, and Chiron Medical CRO standard operating procedures.
2. Perform source data verification, ensuring accuracy and integrity of clinical trial data.
3. Collaborate with clinical trial sites to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
4. Prepare and review essential documents, including informed consent forms, site training materials, and study-related documents.
5. Ensure timely resolution of data discrepancies and implement corrective actions as needed.
6. Maintain regular communication with study sites and provide support as needed throughout the duration of the trial.
7. Assist in the development and review of clinical trial protocols and monitoring plans.

Qualifications:

1. Bachelor's degree in a scientific or healthcare-related field.
2. Minimum of 2 years of experience as a Clinical Research Associate.
3. Strong understanding of GCP, ICH guidelines, and relevant regulatory requirements.
4. Excellent organizational and communication skills.
5. Ability to work independently and collaboratively in a team environment.
6. Proficiency in Microsoft Office applications.

How to Apply: Interested candidates are invited to submit their resume, cover letter, and salary expectations to [e-mail]. Please include "CRA - Istanbul Application" in the subject line of your email.

Chiron Medical CRO is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

We thank all applicants for their interest; however, only those selected for an interview will be contacted.

Sincerely,

Chiron Medical CRO HR Team