About Company
Syneos Health is the only fully integrated biopharmaceutical solutions organization. Our company is purpose-built to accelerate customer success. We seamlessly fuse clinical and commercial capabilities to help customers develop and commercialize products faster, smarter, and with greater success. With a global presence and a diverse team of experts, we are committed to improving patient outcomes and driving innovation in healthcare. Join a company that values collaboration, integrity, and provides unparalleled opportunities for professional growth in the dynamic field of clinical research.
Job Description
Are you passionate about making a tangible impact on global health? Do you have a keen interest in clinical trials and a desire to contribute to the development of life-changing therapies? Syneos Health is excited to offer an exceptional opportunity for an aspiring Clinical Research Associate (CRA) to join our team in Israel. This role is perfect for ambitious individuals looking to launch their career in clinical research, as comprehensive training and mentorship will be provided. As a CRA, you will play a crucial role in the oversight of clinical trials, ensuring that studies are conducted in accordance with Good Clinical Practice (GCP) guidelines, standard operating procedures (SOPs), and regulatory requirements. You will be instrumental in safeguarding patient safety and ensuring the integrity of clinical data. This entry-level position is designed to equip you with the foundational knowledge and practical skills necessary to excel in the CRA profession. You will work closely with experienced CRAs and study teams, gaining hands-on experience in trial monitoring, site management, and regulatory compliance. If you are a highly motivated, detail-oriented individual with a scientific background and excellent communication skills, we encourage you to apply and begin a rewarding career journey with Syneos Health.
Key Responsibilities
- Participate in comprehensive training programs to develop a strong understanding of clinical trial processes, GCP, and regulatory requirements.
- Assist in the preparation, initiation, monitoring, and close-out of clinical study sites in Israel.
- Conduct on-site and remote monitoring visits to ensure protocol adherence, data accuracy, and patient safety.
- Verify that informed consent is properly obtained and documented from all study participants.
- Review source documentation and Case Report Forms (CRFs) for accuracy, completeness, and consistency.
- Identify and resolve discrepancies in clinical data in collaboration with site staff.
- Ensure all essential documents are complete, accurate, and filed appropriately.
- Provide ongoing support and training to investigational site staff regarding study protocols and procedures.
- Prepare clear and concise monitoring visit reports and follow-up letters.
- Communicate effectively with study team members, investigators, and other stakeholders.
- Assist with the collection and submission of regulatory documents as required.
Required Skills
- Bachelor's degree in a life science, health-related field, or equivalent education.
- Strong organizational skills and meticulous attention to detail.
- Excellent written and verbal communication skills in English and Hebrew.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
- Ability to travel extensively within Israel (and occasionally internationally) as required.
- Demonstrated ability to learn new concepts quickly and adapt to changing environments.
- Proactive attitude and a strong work ethic.
- Valid driver's license.
Preferred Qualifications
- Master's degree in a relevant scientific or health-related discipline.
- Previous experience in a clinical setting (e.g., as a research coordinator, nurse, or lab technician).
- Familiarity with medical terminology and clinical research principles.
- Knowledge of ICH-GCP guidelines.
- Ability to work independently and as part of a collaborative team.
Perks & Benefits
- Comprehensive paid training and mentorship program.
- Competitive salary and performance-based bonuses.
- Health and wellness benefits package.
- Generous paid time off.
- Opportunities for rapid career advancement within a global organization.
- Access to cutting-edge technology and innovative clinical research methodologies.
- Professional development and continuing education support.
- Dynamic and supportive work environment.
How to Apply
Interested candidates are encouraged to apply by clicking the application link below. Please ensure your resume highlights relevant educational background and any experience that demonstrates your attention to detail and ability to learn quickly. We look forward to reviewing your application.