Medical Director
Iovance Biotherapeutics, Inc.
full-time
Posted on:
Location Type: Remote
Location: Remote • 🇺🇸 United States
Visit company websiteJob Level
Lead
Tech Stack
Assembly
About the role
- Directs protocol implementation including site identification and communication, attendance at investigators’ meetings, correspondence with sites including IRBs and interaction with operations teams.
- Manages program development, including working cross-functionally with all of the disciplines necessary for successful drug/therapy development: pre-clinical, manufacturing, quality assurance, regulatory, medical affairs, legal, biostatistics and data management, pharmacovigilance, and clinical operations.
- Interacts closely with the pre-clinical team, to understand the scientific basis of targeted therapy, and to apply this knowledge to articulating therapeutic strategies.
- Monitors clinical trials including the oversight of all aspects of trial conduct and safety, contact with investigators and site study staff.
- Supports data analysis and assembly, including clinical study report writing, contributes to the preparation of abstracts, presentations, and manuscripts.
- Interacts closely with Medical Affairs in support of ISTs and publications.
- Interacts closely with the Regulatory group and regulatory agencies, taking part in regulatory submissions, investigator brochure authorship and communication with US and international regulatory agencies.
- Must adhere to Iovance Biotherapeutics’ core values, policies, procedures, and business ethics.
- Perform miscellaneous duties as assigned.
Requirements
- Board Certified MD with minimum of 2-5 years of industry experience.
- Effective oral and written communication skills and excellent interpersonal skills with demonstrated ability to work with a team.
- Demonstrated independence, initiative and the ability to work well in a fast-paced environment.
- Subspecialty training in oncology and/or hematopoietic transplantation preferred.
- Outstanding academic achievement and significant clinical trial experience preferred.
Benefits
- Reasonable accommodations may be made upon request to enable individuals to perform essential functions.
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
clinical trial managementdata analysisclinical study report writingregulatory submissionsinvestigator brochure authorshippharmacovigilancebiostatisticsquality assurancedrug developmenttherapeutic strategies
Soft skills
oral communicationwritten communicationinterpersonal skillsteamworkindependenceinitiativeadaptabilityfast-paced environment
Certifications
Board Certified MD