O pozici
When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
Co budeš dělat
- Medical Monitoring Delivery & Pharmacovigilance Support Independently deliver all medical support required for successful project delivery according to contracted agreements with sponsors, fulfilling all assigned tasks and timelines
- Actively participate in study planning with feasibility leaders and solution consultants
- Participate in team project meetings and investigator meetings
- Provide training to study teams on therapeutic area indication and protocol (excluding direct medical advice on patient care or management)
- Participate in the development and review of study documents including clinical protocols, Medical Monitoring Plans, integrated clinical and statistical summary reports, safety plans, and Informed Consent Forms
- Deliver medical monitoring activities according to Medical Monitoring Plans during study conduct
- Provide medical leadership to projects in close coordination with the Project Leader, serving as either Global Lead Physician or Regional Lead Physician as assigned
- Provide medical input into pharmacovigilance workflows and participate in safety processing, including medical review of serious adverse events
- Client Relationship Building & Engagement Support business development efforts with medical expertise
- Provide medical expertise to clients across multiple channels and interactions
- Offer consultancy on protocol development and drug development programs
- Conduct medical review of various documents that may be audited by clients and regulatory agencies
Koho hledáme
- Medical qualification from an acknowledged medical school
- Minimum 5+ years of clinical medicine and practice experience
- Qualified Psychiatrist or Neurologist, with up to date knowledge and expertise
- Experience as a medical monitor, ideally from another CRO
- Background in clinical aspects of drug development, including medical monitoring and study design/execution
- Knowledge of the drug development process including drug safety; experience in Pharmaceutical Medicine; experience leading, mentoring, and managing individuals or teams
- Excellent English language skills (written and spoken)
Benefity
- Opportunity to work on diverse, innovative clinical research projects
- Professional development and mentoring opportunities
- Potential for leadership and team management roles
- Competitive compensation and benefits package
- Collaborative working environment with leading clinical research professionals
