Associate Director, Regulatory CMC

Solid Biosciences; Boston (MA); Hybrid; USD 170,000 - 220,000; Full time

Benefits offered by this job

Competitive health and dental programs

401(k) with company match

Paid tuition reimbursement

Onsite gym

Daily subsidized lunch

Employee stock purchase plan

Job summary

A genetic medicine company in Boston is seeking an Associate Director of Regulatory CMC to lead regulatory strategy and bridge development with regulatory roles. This hybrid position requires strong regulatory affairs experience in biotechnology, excellent communication skills, and the ability to work collaboratively across teams. The ideal candidate will handle CMC content for clinical trials and engage with agency interactions. The role offers competitive compensation between $170,000 and $220,000 along with extensive benefits.

Qualifications

• Minimum of 4 years of experience in regulatory affairs in the pharmaceutical/biotech.
• Knowledge of recombinant manufacturing processes required.
• Strong knowledge of US and EU regulations pertaining to biological product development.

Responsibilities

• Lead CMC content for global clinical trial applications.
• Collaborate with cross-functional teams to refine product development strategy.
• Drive and contribute to regulatory CMC content and submissions.

Skills

Regulatory affairs experience

Communication skills

Organizational skills

Collaborative teamwork

Problem-solving abilities

Education

Bachelor’s degree in a scientific discipline

Masters, PharmD, or PhD preferred

Job description

Associate Director, Regulatory CMC – Solid Biosciences

Charlestown, MA HQ

Solid Biosciences is a precision genetic medicine company focused on advancing a portfolio of gene therapy candidates targeting rare neuromuscular and cardiac diseases, including Duchenne muscular dystrophy (Duchenne), Friedreich’s ataxia (FA), catecholaminergic polymorphic ventricular tachycardia (CPVT), TNNT2-mediated dilated cardiomyopathy, BAG3-mediated dilated cardiomyopathy, and additional fatal, genetic cardiac diseases. We are advancing a diverse pipeline and delivery platform in the pursuit of uniting experts in science, technology, disease management, and care.

Patient-focused and founded by those directly impacted by Duchenne, Solid’s mission is to improve the daily lives of patients living with devastating rare diseases.

Chemistry, manufacturing and controls is at the forefront of development of our programs and regulatory CMC provides a leadership role in program teams and bridges CMC development and regulatory strategy.

We are seeking an Associate Director of Regulatory Strategy based in Charlestown with a hybrid option. We are seeking a creative and agile regulatory professional who is keen to be a part of a collaborative team with a goal to develop global regulatory CMC experience in gene therapy drug development. The candidate will play an active role in agency interactions, applications, and innovative CMC development solutions in the rare disease space.

The role will lead regulatory CMC on SGT-003 as it moves into later stage development at a vital time in the program. The role offers wide exposure across the internal Solid teams as well as the opportunity to contribute to strategic reviews with senior management. In addition to contributing to the regulatory strategy and process internally, we are seeking a candidate with strong interest in participating in trade organizations to contribute to shaping the broader regulatory community.

This role will report to Head of Regulatory CMC and will be based in Solid’s Corporate Headquarters located in Hood Park in Charlestown, MA and is a hybrid position.

Key Position Responsibilities

• Actively represent Regulatory CMC on interdisciplinary teams (e.g. CMC Teams, Program Teams) and with business partners such as consultants, CDMOs etc.
• Collaborate with cross-functional teams to generate and refine the product development strategy.
• Lead CMC content for global clinical trial applications including the preparation of INDs/CTAs/GMOs and amendments, responses to agency questions, and maintenance activities. Prepare for later stage submission activities.
• Interface with CMC and quality teams, including execution of change management and data integrity processes.
• Drive and contribute to regulatory CMC content and submissions, including necessary cross functional teams and timelines, relevant to assigned projects or programs.
• Actively contribute to the preparation and execution of global agency meetings.
• Support development and implementation of global regulatory CMC strategies, including identifying regulatory risks, to facilitate the progress of programs through all phases of development.
• Represent Solid Bio Regulatory through participation in pharmaceutical trade groups and meetings.

Experience Requirements

• Bachelor’s degree in a scientific discipline; Masters, PharmD, or PhD preferred. Minimum of 4 years of experience in regulatory affairs in the pharmaceutical/biotech, including IND activity, global CTAs, BLAs/MAAs and Agency briefing documents in US and ex-US.
• Knowledge of recombinant manufacturing processes and controls required, with preference for mammalian culture processes.
• Experience in gene therapy programs (rAAV) and rare disease programs a plus, although not required.
• Strong knowledge of US and EU regulations and Guidances pertaining to the CMC aspects of biological product development.
• Experience in submission management and change management required.

Key Position Attributes

• Ability to effectively organize and prioritize tasks to achieve established deadlines.
• Ability to work both independently and within project teams, committees, etc. to achieve group goals, including face to face and remote interactions.
• Excellent verbal and written communication skills. Ability to author and edit CMC content.
• Excellent organizational and program management skills that ensure timely completion of objectives by appropriate prioritization, scheduling and assignment of tasks.
• Strong collaborator with multi-disciplinary teams.
• Creative problem solving and strategizing abilities.

Compensation

The base compensation range for this role is: $170,000-220,000

Base salary offered is determined through an internal analysis utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.

Regular employees are eligible to receive both short-term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward individual performance and align incentives to Solid’s long term company performance.

Benefits and Solid Advantages

• Competitive Health and Dental programs with flexible plan offerings, including FSA and HSA programs
• 401(k) program participation with competitive company matched contributions
• Eligibility to participate in Solid’s Employee Stock Purchase Plan
• Mobile phone subsidy for eligible employees
• Tuition Reimbursement
• Vision Coverage
• Life Insurance
• Voluntary Pet Insurance
• Employee Discount Program on Travel, Entertainment, and Services
• Daily Subsidized Lunch Delivery (onsite @Hood Park)
• Free Onsite Full-Service Gym (onsite @Hood Park)
• Employee Parking (onsite @Hood Park)

Seniority Level

Mid-Senior level

Employment Type

Full-time

Job Function

Research and Manufacturing

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