Clinical Research Coordinator
3 days ago
Adana, 01, Türkiye
Apsida Life Science
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Job title:
Clinical Research Coordinator
Location:
Turkey (multiple locations) Work Arrangement: On-Site Contract Duration: 12 months Therapeutic Area: Oncology Company Overview: Apsida Life Science is partnering with a leading global healthcare and clinical research services organization that provides specialized support to pharmaceutical, biotechnology, and healthcare companies throughout the clinical development process. The organization delivers patient-focused and site-based services across a range of therapeutic areas, supporting the successful execution of clinical trials while maintaining high standards of quality, compliance, and patient care. Key Responsibility:
- Coordinate and support clinical trial activities at assigned sites.
- Work closely with investigators, site staff, sponsors, and other study stakeholders.
- Support patient visits and study procedures in accordance with the study protocol.
- Maintain accurate and timely study documentation and records.
- Support data collection and ensure relevant information is captured accurately.
- Assist with study start-up, ongoing study activities, and close-out activities as required.
- Ensure activities are conducted in accordance with GCP, protocol requirements, SOPs, and applicable regulations.
- Communicate study updates, issues, and site requirements to the relevant projectteam.
- Support monitoring visits, audits, and inspections where required.
Requirements:
- Previous experience as a Clinical Research Coordinator / Study Coordinator.
- Experience working within clinical trials.
- Oncology experience is highly preferred.
- Experience in NSCLC and/or PDAC would be an advantage.
- Good understanding of ICH-GCP and clinical trial requirements.
- Strong organizational and communication skills.
- Ability to work independently while collaborating effectively with site and study teams.
- Willingness and availability to provide on-site support as required. If you are interested in learning more, please reach out to KG Mphahlele at Apsida Life Science: kgmphahlele@apsida.com +44 744 134 1041 Apsida Life Science is a specialist recruitment business based in London (UK), Redhill (UK), Boston (USA) & Pretoria (South Africa) that is dedicated to delivering the best talent to the Life Science industry. We believe there is a gap in the market for a cost-effective, high-quality, and trusted recruitment service that puts the candidate journey at the heart of the recruitment process.
Location:
Turkey (multiple locations) Work Arrangement: On-Site Contract Duration: 12 months Therapeutic Area: Oncology Company Overview: Apsida Life Science is partnering with a leading global healthcare and clinical research services organization that provides specialized support to pharmaceutical, biotechnology, and healthcare companies throughout the clinical development process. The organization delivers patient-focused and site-based services across a range of therapeutic areas, supporting the successful execution of clinical trials while maintaining high standards of quality, compliance, and patient care. Key Responsibility:
- Coordinate and support clinical trial activities at assigned sites.
- Work closely with investigators, site staff, sponsors, and other study stakeholders.
- Support patient visits and study procedures in accordance with the study protocol.
- Maintain accurate and timely study documentation and records.
- Support data collection and ensure relevant information is captured accurately.
- Assist with study start-up, ongoing study activities, and close-out activities as required.
- Ensure activities are conducted in accordance with GCP, protocol requirements, SOPs, and applicable regulations.
- Communicate study updates, issues, and site requirements to the relevant projectteam.
- Support monitoring visits, audits, and inspections where required.
Requirements:
- Previous experience as a Clinical Research Coordinator / Study Coordinator.
- Experience working within clinical trials.
- Oncology experience is highly preferred.
- Experience in NSCLC and/or PDAC would be an advantage.
- Good understanding of ICH-GCP and clinical trial requirements.
- Strong organizational and communication skills.
- Ability to work independently while collaborating effectively with site and study teams.
- Willingness and availability to provide on-site support as required. If you are interested in learning more, please reach out to KG Mphahlele at Apsida Life Science: kgmphahlele@apsida.com +44 744 134 1041 Apsida Life Science is a specialist recruitment business based in London (UK), Redhill (UK), Boston (USA) & Pretoria (South Africa) that is dedicated to delivering the best talent to the Life Science industry. We believe there is a gap in the market for a cost-effective, high-quality, and trusted recruitment service that puts the candidate journey at the heart of the recruitment process.