Company Description

Biogen’s West Coast Hub, based in South San Francisco, is specifically focused on transforming the lives of patients with severe immune-mediated diseases by developing novel targeted therapies with outsized clinical impact, faster. To accomplish this, we are seeking top talent to join us on our journey.

Job Description

About This Role

We are seeking a highly motivated and experienced Medical Director (MD) to support development activities for our portfolio our immunology clinical programs, with a specific emphasis on severe immune-mediated diseases related to glomerular kidney disease. Reporting directly to the Clinical Development Lead the MD and as a key member of the clinical development team, you will support the development of our novel therapeutic candidates in late-stage studies. The successful candidate will primarily be involved in activities associated with the design, execution, monitoring, data interpretation, and reporting of clinical studies evaluating novel therapies across target indications. Additional responsibilities involve managing external collaborations, gaining comprehensive knowledge of the literature related to the product(s) in development, supporting Regulatory interactions, and supporting Medical Affairs and Commercial colleagues. 

As part of a startup environment, the role involves extensive matrix interactions with colleagues from various disciplines to ensure the successful execution of clinical development plans and regulatory filings.

What You Will Do

Support the design and execution of clinical development plans for HI-Bio's programs within rare autoimmune and nephrology therapeutic areas, ensuring alignment with strategic objectives and timelinesProvide medical and scientific oversight for clinical trials, including protocol development, study monitoring, data review, and analysisCollaborate with Clinical Operations in trial setup, conduct, recruitment activities, closeout, and reportingDraft and coordinate completion of clinical study reportsPrepare responses to questions from Ethics Committees and Health AuthoritiesSupport integrated document development for marketing authorization filingInterpret, report, and prepare oral and written results of product research, in collaboration with senior clinical personnel, in preparation for health authority submissionsSupport preparation for FDA Advisory Committee and EU Oral ExplanationProvide leadership to cross-functional project teams with peers from clinical operations, biometrics, clinical pharmacology, biomarker sciences, regulatory affairs, and medical writing, and othersEstablish and maintain relationships with key opinion leaders and clinical investigators in the nephroimmunology field and disease areas related to clinical development programsEnsure compliance with regulatory requirements and guidelinesCollaborate with cross-functional teamsParticipate in due diligence activities and provide medical expertise in support of business development initiatives as neededRepresent HI-Bio externally at scientific conferences, investor meetings, and other industry events

  For the right candidate we are open to remote hires.

Who You Are

You have significant experience in clinical trials and can strongly communicate and present relevant clinical data to leadership and core teams. You are curious, creative and collaborative with a passion for improving the lives of patients with Rare Autoimmune Nephrology.

 

Qualifications

Required Skills

MD or equivalent degree, with board certification in nephrology, immunology, or similar field.Minimum of 3+ years of clinical development experience in the pharmaceutical or biotechnology industry, with a track record of successful drug development.Experience in late-stage drug development, with a preference for experience in nephrology and/or immuno-inflammatory indicationsStrong knowledge of clinical trial design and execution, including experience with adaptive trial designs and biomarker-based approachesDeep understanding of regulatory requirements for drug development, including experience leading interactions with global regulatory agenciesExcellent communication skills, with the ability to effectively communicate complex medical and scientific information to diverse audiencesStrong interpersonal skills, with the ability to establish and maintain relationships with key opinion leaders, clinical investigators, and internal stakeholders through a highly collaborative approachAbility to travel domestically and internationally, approximately 10-20% of the time.

 

Additional Information

The base compensation range for this role is $187,000 - $312,000. Base salary is determined by a combination of factors including, but not limited to, job related years of relevant experience, internal equity, and location of the job. Additionally, this role is eligible for participation in Biogen’s LTI grants and other incentive programs. Biogen offers a full range of benefits that include medical, dental, life, long and short-term disability insurances, vacation, end-of-year shutdown, and 401K participation and matching contributions. 

Why Biogen?

We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.

At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.

All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.