Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
💊 Pharmaceuticals
💰 Venture Round on 1990-01
December 4
Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions
10,000+ employees
Founded 1983
⚕️ Healthcare Insurance
🧬 Biotechnology
💊 Pharmaceuticals
💰 Venture Round on 1990-01
• Remote role for CRA in Poland at Parexel. • Responsible for setting up and overseeing clinical studies. • Participate in submission of protocols and assist in regulatory submissions. • Work with top pharmaceutical companies on impactful oncology studies.
• Bachelor’s or equivalent degree in biological science, pharmacy or other health related discipline. • Minimum of 2 years of active independent field monitoring experience - all types of visits and at least 1-year experience monitoring oncology trials. • Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology. • Ability to perform all clinical monitoring activities independently. • Strong interpersonal, written, and verbal communication skills within a matrixed team. • Experience working in a self-driven capacity, with a sense of urgency and limited oversight. • A client-focused approach to work and flexible attitude with respect to assignments/new learning. • The ability to manage multiple tasks, evaluate a variety of unpredictable scenarios and achieve project timelines while being able to apply your understanding of study protocol(s). • An honest and ethical work approach to promote the development of life changing treatments for patients. • Understanding of ICH GCP Compliance. • Excellent time management and social skills. • Highly motivated with a phenomenal eye for detail. • Ability to travel domestically and internationally approximately 65%-75% of working time. • Expected travelling ~2-3 days/week. • Current driver’s license required.
• Premium salary. • Car or car allowance. • Paid holidays. • Medical care plan: Health, Dental & Vision. • Life Assurance. • Company cell phone and equipment. • Market leading PTO. • Culture of teamwork and collaboration. • People who motivate and face challenges together. • Innovative technology. • Excellent training.
Apply NowNovember 8
201 - 500
Lead CRA develops relationships and oversees clinical site project tasks for ocular research.
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Manage clinical research sites for KCR's clinical trials across Europe.