Medical Director, Autoantibody, Pipeline - US Medical Affairs

About the role

We are searching for the best talent for Medical Director, Autoantibody Medical Affairs within our US Immunology Medical Affairs organization located in Horsham, PA.

Responsibilities

• Contribute to the strategic planning and execution of Phase IIIb & IV trials, post-marketing requirement studies, investigator initiated or collaborative studies, serving as a study responsible physician/scientist (SRP/SRS) for select medical affairs trials.
• Contribute/lead the advancement of protocol development, medical / data monitoring, study operations, data analysis / reporting, writing of study reports and publications, as applicable.
• Partner with colleagues on real-world evidence, health economic and outcomes research, biostatistics, and work with commercial marketing colleagues through integrated evidence teams and other touchpoints to formulate and execute activities in support of the Autoantibody TA strategy across the asset, prioritizing key indications, with a focus on maternal fetal medicine and warm autoimmune hemolytic anemia.

Requirements

• MD, DO, PhD or PharmD degree is required.
• At least 8-10 years total healthcare related experience (academic clinical research, clinical practice, and/or pharmaceutical industry) with at least 2 years of experience with clinical study, registry, or real-word evidence, prior commercial/medical launch experience is preferred.
• Pharma industry experience is highly preferred; Medical Affairs experience is a strong asset.
• Experience in clinical trial design (Phase IIIb & IV) and clinical data interpretation is required.
• Prior experience in clinical research and exposure to industry partnered activities are strongly preferred.
• Experience in scientific investigation into mechanisms of autoimmune/alloimmune disease preferred.
• Excellent attention to detail and organization skills are vital for this position.
• Experience interacting with health care professionals and other thought leaders is a strong asset.
• Evidence of strong scientific writing skills and analytical thinking is essential.
• Ability to work in a matrix environment is essential for success in this role.
• Up 25% travel (primarily domestic & limited international) is required.

Qualifications

• This position is located in Horsham, PA and follows a hybrid schedule of three days in the office and two days remotely per week.

Benefits

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via this link, internal employees contact AskGS to be directed to your accommodation resource.