Medical Director / Senior Medical Director - Hematology/oncology(remote)
PPD (Thermo Fisher)
Remote, , UK
Remote
Hematology/oncology specialization
Medical oversight of clinical trials
Serious adverse event review
PPD (Thermo Fisher) is seeking a Medical Director/Senior Medical Director for Hematology/Oncology, a remote position responsible for overseeing clinical trials and ensuring compliance with medical standards and regulations. The ideal candidate will hold an MD with specialization in Oncology or Hemato-Oncology and possess relevant clinical and industry experience
Job Summary
Provides medical oversight of clinical trials to ensure company SOPs, client directives, good clinical practice, and regulatory requirements are followed.
Attends and presents at investigator and sponsor meetings, provides medical consultation to clients, investigators and project team members and supports business development activities.
Performs data review including review of coding listings and/or full safety data to assess for potential safety concerns and assists in writing and/or review of CSR, IND/NDA report, ICSR, signal detection reports, periodic reports, RMP, REMS, CTD modules, etc.
Matching Summary
Match Score: 85
PPD (Thermo Fisher) is seeking a Medical Director/Senior Medical Director for Hematology/Oncology, a remote position responsible for overseeing clinical trials and ensuring compliance with medical standards and regulations. The ideal candidate will hold an MD with specialization in Oncology or Hemato-Oncology and possess relevant clinical and industry experience.
Skills & Requirements
Must-have
Hematology/Oncology specialization
Medical oversight of clinical trials
Serious adverse event review
Regulatory requirements adherence
Client and investigator consultation
Nice-to-have
Business development support
Departmental process improvement
Therapeutic training provision
Mentoring and training other staff
Key Requirements
MD or equivalent required
Specialization in Oncology or Hemato-Oncology required
Active medical license preferred
Minimum 2 years clinical experience in specialty
Minimum 1-2 years clinical trial experience in CRO/pharma or as PI
Minimum 2 years direct safety/Pharmacovigilance experience