Parexel yangi dori vositalarini ishlab chiqish jarayonida biofarmatsevtika kompaniyalariga xizmat ko‘rsatuvchi global klinik tadqiqot tashkilotidir. Uning faoliyati I–IV bosqich klinik sinovlari, portfel va tadqiqotlarni boshqarish, tartibga solish strategiyasi, bozorga chiqish hamda hayotiy siklni rejalashtirishni qamrab oladi. 21 000 dan ortiq mutaxassisga ega Parexel klinik, tartibga solish va terapevtik tajribani bemorlar haqidagi tushunchalar hamda innovatsion sinov dizaynlari bilan birlashtiradi. Kompaniya onkologiya, neyrofanlar va kam uchraydigan kasalliklar kabi yo‘nalishlarda tadqiqotlarni qo‘llab-quvvatlaydi hamda klinik ishlab chiqish jarayonini samaraliroq va bemorga yo‘naltirilgan qilishga e’tibor qaratadi.
Clinical Research Associate, Oncology
Monitor oncology clinical trial sites for Parexel, a provider of clinical development, regulatory, consulting, and market access services. Oversee site compliance, participant safety and recruitment, and study documentation.
Tavsif
- Serve as the primary site contact and manager throughout each clinical research study.
- Build strong site relationships and maintain continuity across trial phases.
- Manage and monitor clinical study sites in line with ICH/GCP, sponsor SOPs, applicable laws and regulations, protocols, and monitoring plans.
- Develop a thorough understanding of study protocols and related procedures.
- Coordinate with sponsor colleagues to prepare sites for readiness.
- Contribute to site selection and validation.
- Conduct remote and on-site monitoring and oversight.
- Ensure site data are complete, accurate, and unbiased.
- Safeguard participants’ rights, safety, and well-being.
- Conduct validation, initiation, monitoring, and closeout visits, and submit accurate reports on time.
- Collect, review, and track regulatory documents for study start-up, ongoing maintenance, and closeout.
- Discuss protocol conduct, recruitment, retention, deviations, regulatory documents, audits and inspections, and site performance with investigators and site staff.
- Identify, assess, resolve, and escalate site performance, quality, and compliance concerns.
- Maintain study information and documentation in CTMS, eTMF, and other systems.
- Share process expertise and best practices with the CRA team, including through buddying and mentoring.
- Support or lead audits and inspections.
- Conduct co-monitoring visits when appropriate.
Talablar
- Fluency in English and relevant local languages, spoken and written.
- Sound knowledge of clinical research, trial phases, current GCP/ICH standards, and country-specific clinical research laws and guidance.
- Good knowledge of global and country or regional clinical research guidelines.
- Practical knowledge of Good Documentation Practices.
- Demonstrated site management skills, including oversight of site performance and patient recruitment.
- Strong monitoring skills and the ability to exercise independent professional judgment.
- Proficiency with IT tools, including Microsoft Office and clinical applications.
- Ability to interpret and analyze data and metrics.
- Ability to handle complex issues and find practical solutions.
- Skills in root cause analysis and preventive and corrective actions.
- Strong time management, organization, interpersonal, conflict management, and problem-solving skills.
- Ability to work independently across multiple protocols, sites, and therapy areas.
- Ability to prioritize and manage several tasks at once.
- Ability to work effectively in a multicultural, matrixed environment.
- Commitment to customer focus, quality, and compliance.
- Availability for domestic and international travel about 65%–75% of working time, typically 2–3 days per week.
- Current driver’s license.
- At least two years of direct site monitoring experience in biotechnology, pharmaceuticals, or a CRO.
- Oncology monitoring experience.
- Bachelor’s degree preferred, ideally with a strong science or biology focus.
Imtiyozlar
- Full-time employment.
- Remote work arrangement.
- Equal opportunity employment.