Therapeutic Area Lead Mea Solid Tumor

7 months ago


Dubai, United Arab Emirates ABBVIE Full time

Oncology is a key therapeutic area for AbbVie, with a portfolio consisting of three marketed products — Imbruvica, Venclexta, and Empliciti — and a pipeline containing multiple promising new molecules that are being studied in nearly 200 clinical trials in 19 different types of cancer.

The MEA Lead Solid tumors & companion Diagnostics is responsible for co-planning and executing of the solid tumors, Biomarker and Companion Diagnostics Medical Affairs strategy across the Oncology portfolio in MEA. Works closely with MEA cross-functional affiliate and region teams for coordination of solid tumors, biomarker and companion diagnostic activities and strategy & execution.

The role reports to MEAR regional MD with dotted line reporting to Intercontinental Oncology TA Head

**Key Responsibilities:

- **
- Develop and coordinate the overarching Solid tumor, Biomarker and CDx strategy across projects in Oncology
- Lead the development and implementation of solid tumors, biomarker and diagnostic strategies for individual projects and/or therapeutic areas
- Establish and maintain external engagement/field interactions with key HCPs including and not limited to medical oncologists, pathologists, oncology pharmacists, laboratory stakeholders.
- Lead the relevant oncology, CDx market understanding activities ( understanding epidemiology, mapping external stakeholders, understanding patient and tissue journey, understanding current SoC, guidelines, etc).
- Responsible for understanding the regulatory requirements related to clinical studies and accountable for complying with those requirements. Serves as the scientific team interface for key regulatory discussions.
- May act as medical/scientific leader for projects within an area or across several areas.
- May assist in the development of scientifically accurate marketing materials, medical education programs, advisories, and symposia.
- May assist with the scientific review, development, execution and communication of affiliate/ regional medical affairs sponsored or supported clinical research activities.
- Initiate research projects and drive them to completion, resulting in high quality publications.
- May lead cross functional sub teams responsible for discrete projects within the therapeutic area (individual publications or study collaborations).
- No direct supervisory responsibility. Effectively guide scientific personnel within the matrixed Oncology Therapeutic Area.

**Qualifications & Experience:

- **

**Requirements:

- **
- Advanced education (e.g., MD, PhD, PharmD) required.
- Overall 10 yrs experience in the pharmaceutical industry or equivalent; with at least 3 years of Oncology therapeutic area experience including at least two in medical affairs.
- Experience with CDx development and Immunology-Oncology is desired
- Management and leadership experience at project level, experience with strategic initiatives
- Proven leadership skills in a cross-functional team environment..
- Ability to interact externally and internally to support business strategy.
- Ability to run a clinical study or medical affairs team independently with little supervision.
- Knowledge of clinical trial methodology, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols.
- Must possess excellent oral and written communication skills.
- Ability to work independently establishing foundation of Solid tumors and CDx in MEAR countries.
- The role is 50% office based & 50% field based.
- Travel expectations: 30% of Time



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