We are seeking a medical professional to provide expert input to global clinical studies.
- Collaborate with project teams and sites to deliver high-quality medical services.
- Advise on medical matters for clients, data safety monitoring boards, regulatory agencies, and third-party vendors.
- Review and analyze clinical data, including safety monitoring.
- Participate in the preparation of clinical development plans, protocols, investigator brochures, and clinical study reports.
- Perform medical review of incoming SAE reports, including narrative content and queries.
- Address safety issues across the study from sites and the study team.
- Provide training to project teams and sites.
- Contribute to project risk assessment activities, identify program risks, and create mitigation strategies.
Requirements :
Board certification in HematologyExperience in medical practice and patient careKnowledge of safety review processes, medical terminology, coding dictionaries, and safety regulatory requirementsStrong knowledge of and experience in HematologyFull working proficiency in EnglishProficiency with MS Office applicationsExcellent communication, presentation, and analytical skillsProblem-solving skills, team-oriented, and detail-orientedAbout the Role :
This role offers an opportunity to join our international group of medical professionals and build a career on the frontline of medical science.
You will use your knowledge and expertise to help bring new medications to patients who need them.
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