Associate Medical Director, Rare Movement Disorders — Clinical Leader

Biogen; Cambridge (MA); Presencial; USD 194.000 - 267.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical insurance

Dental insurance

Vision insurance

Life insurance

Paid vacation

Holiday time off

Sick time

Maternity/Parental leave

401(k) match

Employee stock purchase plan

Tuition reimbursement

Professional groups

Descripción de la vacante

Biogen’s Rare Neurology Development Unit (RNDU) in Cambridge, MA, seeks an Associate Medical Director to advance early and late-stage programs for SMA, ALS and rare movement disorders. You will help design trials, interpret results, and guide regulatory interactions across global studies.

You will lead cross-functional teams, contribute to submissions, and support publications while staying current on regulatory guidelines for the field.

Formación

• MD/PhD/PharmD with 5+ years of clinical research experience.
• Experience analyzing and interpreting clinical trials.
• Knowledge of GCP, trial design, biostatistics, and regulatory requirements.
• Strong organizational and project management skills in a global matrix.
• Proven ability to interact with diverse internal and external stakeholders.

Responsabilidades

• Support development and oversight of study protocols and reports.
• Monitor safety and efficacy data for assigned trials.
• Represent development on cross-functional study teams to ensure quality.
• Contribute to regulatory submissions and publications.
• Prepare investigator and advisory board materials with project teams.
• Stay current on regulations and guidelines for the therapeutic area.

Conocimientos

GCP knowledge

Trial design

Regulatory requirements

Biostatistics

Cross-functional collaboration

Project management

Communication skills

Educación

MD/PhD/PharmD

5+ years clinical research experience

Descripción del empleo

Biogen’s Rare Neurology Development Unit (RNDU) in Cambridge, MA, seeks an Associate Medical Director to advance early and late-stage programs for SMA, ALS and rare movement disorders. You will help design trials, interpret results, and guide regulatory interactions across global studies.

You will lead cross-functional teams, contribute to submissions, and support publications while staying current on regulatory guidelines for the field.