Director Jobs

About The Position

Requirements

• BS degree in life sciences.
• Minimum 10 years’ experience in regulatory affairs
• Late-stage experience in oncology drug development.
• Experienced in creating and negotiating the clinical-regulatory aspects of oncology programs.
• Able to write, edit, and/or collaborate on the development of high-quality clinical-regulatory documents. E.g., briefing books, investigator brochures, protocols, clinical study reports, clinical summaries.
• Able to write clearly and concisely, within agreed timelines.
• Able to simultaneously manage multiple projects and submissions, with flexibility to pivot based on new data, program changes, and/or external influences.
• High attention to detail and accuracy.
• High organizational and planning skills.
• Able to influence and negotiate professionally at various levels within cross-functional teams and with external partners, while maintaining positive working relationships.
• Excellent interpersonal, verbal and written communication skills

Nice To Haves

• Advanced degree preferred (PhD, MS, PharmD)
• Experienced in the creation, submission, and negotiation of market applications preferred.

Responsibilities

• Works closely with functional leaders to 1) create the optimal development path for Iovance product candidates, 2) negotiate optimal development paths within internal cross-functional teams and with health authorities, 3) execute clinical-regulatory development plans on-time and while managing all identified risks.
• Plans, manages, and creates Clinical Trial Applications, Market Applications and amendments.
• Ensures that submission documents and correspondence are of the highest quality in terms of content, organization, clarity of writing, and accuracy.
• Leads cross-functional teams in preparing for health authority meetings.
• Ensures that evolving global regulations, guidelines and health authority expectations, especially those related to cell therapies, are incorporated into program decision making.
• Works within the department and with other functional areas on process improvements.
• Must adhere to Iovance Biotherapeutics’ core values, policies, procedures, and business ethics.
• Perform miscellaneous duties as assigned.

Benefits

• Pay Transparency