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What is the role of a Executive Director, Regulatory Affairs CMC at Crescent Biopharma?

The Executive Director, Regulatory Affairs CMC position at Crescent Biopharma is a Full-time or part-time position opportunity in the Executive/Management field.

Where is this Executive Director, Regulatory Affairs CMC job located?

Waltham, Massachusetts, 02451, United States

What type of employment is offered for this Executive Director, Regulatory Affairs CMC role?

Full-time or part-time position

What is the expected salary for this Executive Director, Regulatory Affairs CMC job?

Compensation will be discussed during the hiring process.

Executive Director, Regulatory Affairs CMC job near me in Waltham, Massachusetts at Crescent Biopharma

Executive Director, Regulatory Affairs CMC

Crescent Biopharma’s vision is to build a world leading oncology company bringing the next wave of therapies for cancer patients. The Company’s clinical-stage pipeline includes its lead program, a PD-1 x VEGF bispecific antibody, as well as novel antibody-drug conjugates. By leveraging multiple modalities and established targets, Crescent aims to rapidly advance potentially transformative therapies as single agents and as part of combination regimens to treat a range of solid tumors. For more information, visit www.crescentbiopharma.com and follow the Company on LinkedIn and X.

Responsibilities

Lead and/or oversee global regulatory CMC submissions (e.g., INDs, CTAs, BLAs, MAAs etc.) through product lifecycle.
Proactively identify regulatory risks, opportunities, and mitigation strategies in alignment with objectives, and communicate to management, as needed
Provide strategic regulatory guidance to TechOps and Quality organizations to ensure global compliance and readiness for clinical and commercial supply
Serve as the primary interface with global regulatory agencies for CMC-related negotiations, milestone meetings, and information requests.
Provides global regulatory input and support on product-compliance related activities including change controls, deviations, and investigations.
Manage junior team members and contractors to support development activities

Education & Experience

BS/BA Degree in a Scientific Discipline, Advanced Degree (M.S., Ph.D., etc.) required
12 years’ experience in Regulatory Affairs CMC in Pharma/Biotech
Strong negotiation skills with health authorities (e.g. FDA, EMA) as well as submissions
Experience with leading IND and Marketing Applications
Experience with antibody drug conjugates and biologics
Strong analytical, strategic thinking, and problem-solving skills.
Excellent communication and leadership abilities; able to influence across all levels of the organization.
Ability to thrive in a fast-paced, ambiguous environment while managing competing priorities.
Commitment to fostering a diverse and inclusive workplace

What We Offer

Opportunity to join a mission-driven team where you'll contribute to impactful work, take on varied responsibilities, and grow quickly in a dynamic environment
Competitive compensation, including base salary, performance bonus, and equity
100% employer-paid benefits package
Flexible PTO; also, two, one-week company-wide shutdowns each year
A commitment to your professional development, with access to resources, mentorship, and growth opportunities

Salary Range

The salary range for this position is $290,000 to $323,000. The final salary offered will depend on several factors, which may include, but is not limited to relevant years of experience, educational background, and geography.

Additional Description for Pay Transparency:

The final salary offered will depend on several factors, which may include, but is not limited to relevant years of experience, educational background, and geography. Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability. Subject to the terms of their respective plans, employees are eligible to participate in the Company’s savings plan (401(k)). This position is eligible to participate in the Company’s long-term incentive program. Subject to the terms of their respective policies and date of hire, Employees are eligible for the following time off benefits: Vacation – Unlimited PTO; Sick time – 10 days per calendar year; Holiday pay, including two Company shut downs; Parental Leave – 16 weeks within one year of the birth/adoption/foster care of a child; FMLA; Military Leave. Additional information can be found - https://www.crescentbiopharma.com/careers/#benefits

Please note:

Crescent Biopharma is an Equal Opportunity Employer. We are committed to fostering a diverse, inclusive, and equitable workplace where all individuals are valued and respected. Employment decisions are based on qualifications, merit, and business needs, without regard to race, color, religion, gender, sexual orientation, national origin, disability, veteran status, or any other protected status.

Please note, Crescent does not accept unsolicited resumes from external agencies or recruiters. Submission of a resume without a prior written agreement does not create any express or implied contract between Crescent and the agency. Crescent will not pay any fees related to unsolicited resumes.

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Executive Director, Regulatory Affairs CMC in Waltham, Massachusetts at Crescent Biopharma

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