Medical Director - Biotech - MA

Waltham Permanent USD180,000 - USD230,000
  • Assist in managing assets in company development portfolio
  • Join a fast paced, growing Clinical Biopharmaceutical Company

About Our Client

Our client is a clinical-stage biopharmaceutical company focusing on neuromuscular diseases. Their mission is to discover and develop these differentiated therapeutics which treat patients that do not have a current alternative. This publicly traded company was founded in the past decade and has massive growth potential.

Job Description

MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.


  • Prepare the clinical development plans, in conjunction with other relevant functional areas
  • Participate in the development of study protocols, statistical analysis plans, investigators brochures, and other key study documents in conjunction with other line functions and with minimal guidance
  • Serve on cross-functional study teams for assigned trials, working with other team members to achieve efficient, high-quality study execution, and data analysis
  • Participate in the preparation of regulatory documents in support of regulatory submissions, including clinical section of INDs and CTAs, safety reports, responses to regulatory authorities, clinical study reports, and other documents as appropriate Interface with regulatory authorities as appropriate
  • Act as liaison between clinical development and other internal groups for assigned studies
  • Provide medical and development leadership for cross-functional teams
  • Represent company to outside medical personal in the development of clinical protocols and study conduct

The Successful Applicant

  • MD, or DO Board certification/eligibility in hematology is highly desired
  • Minimum of 2 years Pharmaceutical/Biotech industry experience, including time managing clinical trials and clinical development programs
  • Global clinical research experience and experience interacting with regulatory authorities is a plus
  • Ability to work collaboratively in a fast-paced, team-based Matrix environment
  • Ability to work independently to resolve challenges
  • Excellent oral and written communication skills

What's on Offer

  • Amazing Stock options
  • Annual bonus
  • Excellent benefits package
  • Novel drug portfolio with strong pipeline
  • Start up culture
  • Contribute to development of cutting edge treatments for rare diseases
Connor Colombo
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Job summary

Life Sciences
Sub Sector
Healthcare / Pharmaceutical
Contract Type
Consultant name
Connor Colombo
Job Reference