Director, Regulatory Affairs CMC
$207K - $253K/yr
Applies expert regulatory CMC knowledge to address and overcome challenges that arise during development and commercialization. * Guides the team in defining and driving the strategy for CMC ...
$207K - $253K/yr
Applies expert regulatory CMC knowledge to address and overcome challenges that arise during development and commercialization. * Guides the team in defining and driving the strategy for CMC ...
$207K - $253K/yr
Applies expert regulatory CMC knowledge to address and overcome challenges that arise during development and commercialization. * Guides the team in defining and driving the strategy for CMC ...
Waltham, MA · On-site
$207K - $253K/yr
Applies expert regulatory CMC knowledge to address and overcome challenges that arise during development and commercialization. * Guides the team in defining and driving the strategy for CMC ...
Waltham, MA · On-site
$207K - $253K/yr
Applies expert regulatory CMC knowledge to address and overcome challenges that arise during development and commercialization. * Guides the team in defining and driving the strategy for CMC ...
Somerville, MA · Hybrid
$163K - $216K/yr
Position Description The Senior Director, Regulatory CMC is responsible for defining and executing global CMC regulatory strategy for approved and late-stage gene therapy products, with a strong ...
Somerville, MA · Hybrid
$163K - $216K/yr
Position Description The Senior Director, Regulatory CMC is responsible for defining and executing global CMC regulatory strategy for approved and late-stage gene therapy products, with a strong ...
Norwood, MA · On-site
The Role CMC is seeking a dynamic and experienced Director, CMC Stability to lead an end-to-end stability function spanning non-clinical-enabling, clinical, and commercial programs. This leader will ...
Norwood, MA · On-site
The Role CMC is seeking a dynamic and experienced Director, CMC Stability to lead an end-to-end stability function spanning non-clinical-enabling, clinical, and commercial programs. This leader will ...
$161K - $212K/yr
Prepares CMC regulatory strategies that enable first pass approvals. Develops and manages content strategy for regulatory submissions, including INDs/CTAs and amendments, new marketing applications ...
Quick apply
$161K - $212K/yr
Prepares CMC regulatory strategies that enable first pass approvals. Develops and manages content strategy for regulatory submissions, including INDs/CTAs and amendments, new marketing applications ...
Waltham, MA · On-site
$160K/yr
Prepares CMC regulatory strategies that enable first pass approvals. Develops and manages content strategy for regulatory submissions, including INDs/CTAs and amendments, new marketing applications ...
Waltham, MA · On-site
$160K/yr
Prepares CMC regulatory strategies that enable first pass approvals. Develops and manages content strategy for regulatory submissions, including INDs/CTAs and amendments, new marketing applications ...
Position Summary The Principal Scientist, Regulatory CMC will report to the Director, Regulatory CMC and be responsible for participating in the development of global Chemistry, Manufacturing and ...
Position Summary The Principal Scientist, Regulatory CMC will report to the Director, Regulatory CMC and be responsible for participating in the development of global Chemistry, Manufacturing and ...
North Chicago, IL · On-site
$144K - $190K/yr
Prepares CMC regulatory strategies that enable first pass approvals. Develops and manages content strategy for regulatory submissions, including INDs/CTAs and amendments, new marketing applications ...
North Chicago, IL · On-site
$144K - $190K/yr
Prepares CMC regulatory strategies that enable first pass approvals. Develops and manages content strategy for regulatory submissions, including INDs/CTAs and amendments, new marketing applications ...
North Chicago, IL · On-site
$144K - $190K/yr
Prepares CMC regulatory strategies that enable first pass approvals. Develops and manages content strategy for regulatory submissions, including INDs/CTAs and amendments, new marketing applications ...
North Chicago, IL · On-site
$144K - $190K/yr
Prepares CMC regulatory strategies that enable first pass approvals. Develops and manages content strategy for regulatory submissions, including INDs/CTAs and amendments, new marketing applications ...
Norwood, MA · On-site
The Role CMC is seeking a dynamic and experienced Director, CMC Stability to lead an end-to-end stability function spanning non-clinical-enabling, clinical, and commercial programs. This leader will ...
Norwood, MA · On-site
The Role CMC is seeking a dynamic and experienced Director, CMC Stability to lead an end-to-end stability function spanning non-clinical-enabling, clinical, and commercial programs. This leader will ...
$144K - $190K/yr
Prepares CMC regulatory strategies that enable first pass approvals. Develops and manages content strategy for regulatory submissions, including INDs/CTAs and amendments, new marketing applications ...
Quick apply
$144K - $190K/yr
Prepares CMC regulatory strategies that enable first pass approvals. Develops and manages content strategy for regulatory submissions, including INDs/CTAs and amendments, new marketing applications ...
San Francisco, CA · On-site
$195K - $272K/yr
As a member of the CMC project teams, provide strategic CMC regulatory leadership to develop and execute sound regulatory strategies that meet global regulatory requirements and enable Vir business ...
San Francisco, CA · On-site
$195K - $272K/yr
As a member of the CMC project teams, provide strategic CMC regulatory leadership to develop and execute sound regulatory strategies that meet global regulatory requirements and enable Vir business ...
North Chicago, IL · On-site
$144K - $190K/yr
Prepares CMC regulatory strategies that enable first pass approvals. Develops and manages content strategy for regulatory submissions, including INDs/CTAs and amendments, new marketing applications ...
North Chicago, IL · On-site
$144K - $190K/yr
Prepares CMC regulatory strategies that enable first pass approvals. Develops and manages content strategy for regulatory submissions, including INDs/CTAs and amendments, new marketing applications ...
$161K - $213K/yr
Prepares CMC regulatory strategies that enable first pass approvals. Develops and manages content strategy for regulatory submissions, including INDs/CTAs and amendments, new marketing applications ...
Quick apply
$161K - $213K/yr
Prepares CMC regulatory strategies that enable first pass approvals. Develops and manages content strategy for regulatory submissions, including INDs/CTAs and amendments, new marketing applications ...
This role involves coordinating and preparing CMC sections of regulatory submissions to support RevMed's global clinical trials, market applications and post approval changes. The ideal candidate ...
This role involves coordinating and preparing CMC sections of regulatory submissions to support RevMed's global clinical trials, market applications and post approval changes. The ideal candidate ...
San Diego, CA · On-site +1
Travere is seeking an Executive Director, CMC Diligence to lead the CMC assessments of clinical/commercial-stage assets associated with external business development opportunities. This individual ...
San Diego, CA · On-site +1
Travere is seeking an Executive Director, CMC Diligence to lead the CMC assessments of clinical/commercial-stage assets associated with external business development opportunities. This individual ...
Billerica, MA · On-site
$134K - $202K/yr
HC-RD-RCD1 Reg CMC LM Marketed 1 Recruiter:Sarah Ellis This information is for internals only. Please do not share outside of the organization. Your Role: The Senior Manager Regulatory CMC (RCMC) is ...
Billerica, MA · On-site
$134K - $202K/yr
HC-RD-RCD1 Reg CMC LM Marketed 1 Recruiter:Sarah Ellis This information is for internals only. Please do not share outside of the organization. Your Role: The Senior Manager Regulatory CMC (RCMC) is ...
South San Francisco, CA · On-site
$275K - $280K/yr
The Director of Regulatory CMC will lead the development and execution of global CMC regulatory strategies for our pipeline of small molecules and monoclonal antibodies to accelerate clinical ...
South San Francisco, CA · On-site
$275K - $280K/yr
The Director of Regulatory CMC will lead the development and execution of global CMC regulatory strategies for our pipeline of small molecules and monoclonal antibodies to accelerate clinical ...
Position Summary The Principal Scientist, Regulatory CMC will report to the Director, Regulatory CMC and be responsible for participating in the development of global Chemistry, Manufacturing and ...
Position Summary The Principal Scientist, Regulatory CMC will report to the Director, Regulatory CMC and be responsible for participating in the development of global Chemistry, Manufacturing and ...
Waltham, MA · On-site
$200K - $240K/yr
This individual will work closely with the CMC, Quality Assurance, Clinical Drug Supply, and Regulatory Affairs teams to ensure the successful planning, development, and delivery of CMC regulatory ...
Waltham, MA · On-site
$200K - $240K/yr
This individual will work closely with the CMC, Quality Assurance, Clinical Drug Supply, and Regulatory Affairs teams to ensure the successful planning, development, and delivery of CMC regulatory ...
$18.48 is the 25th percentile. Wages below this are outliers.
$13.94 - $18.77
27% of jobs
The median wage is $23.39 / hr.
$18.77 - $23.60
24% of jobs
$23.60 - $28.43
18% of jobs
$31.75 is the 75th percentile. Wages above this are outliers.
$28.43 - $33.26
9% of jobs
$33.26 - $38.09
6% of jobs
$38.09 - $42.92
9% of jobs
$42.92 - $47.75
4% of jobs
$47.75 - $52.58
2% of jobs
$52.58 - $57.41
0% of jobs
$57.41 - $62.24
1% of jobs
$62.24 - $67.07
0% of jobs
$13
$31
$67
| Aspect | CMC | Regulatory Affairs Specialist |
|---|---|---|
| Required Credentials | Bachelor's degree in life sciences, chemistry, or pharmacy; often additional certifications in pharmaceutical sciences | Bachelor's degree in life sciences, pharmacy, or related field; certifications in regulatory affairs are common |
| Work Environment | Laboratories, manufacturing sites, and R&D departments within pharmaceutical companies | Regulatory agencies, pharmaceutical companies, and consulting firms |
| Industry Usage | Focuses on drug development, manufacturing, and quality documentation | Focuses on compliance, submissions, and communication with regulatory bodies |
While both CMC and Regulatory Affairs Specialists work within the pharmaceutical industry, CMC professionals primarily handle the chemistry, manufacturing, and control aspects of drug development. Regulatory Affairs Specialists focus on ensuring compliance with regulations and managing submissions to authorities. Both roles often collaborate but serve distinct functions in bringing a drug to market.

$207K - $253K/yr
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 28 days ago
Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can progress to cirrhosis, liver failure, need for liver transplantation and premature mortality. Every member of our Madrigal team is connected by our shared purpose: leading the fight against MASH.
Madrigal's medication, Rezdiffra (resmetirom), is a once-daily, oral, liver-directed THR- agonist designed to target key underlying causes of MASH. Rezdiffra is the first and only medication approved by both the FDA and European Commission for the treatment of MASH with moderate to advanced fibrosis (F2 to F3). An ongoing Phase 3 outcomes trial is evaluating Rezdiffra for the treatment of compensated MASH cirrhosis (F4c).
Our success is driven by our people. We are building a dynamic, inclusive, and high-performing culture that values scientific excellence, operational rigor, and collaboration. To support our continued growth, we are strengthening our workforce strategy to ensure we have the right talent, at the right time, in the right way.
This role provides strategic, tactical and operational regulatory CMC leadership to support clinical trial applications, market registrations and post-approval submissions, along with managing the day-to-day regulatory CMC activities of assigned projects for development and/or commercial products. These activities include acting as a regulatory CMC representative on cross-functions teams, planning regulatory CMC submission strategies, and conducting regulatory CMC intelligence activities.
Key Responsibilities
Required & Desired Qualifications
Madrigal's Total Rewards strategy is based on a biotech industry peer group comparator and is inclusive of base pay, bonus and equity. Our equity offers meaningful opportunity allowing our employees to share in the success they help create. By aligning individual and company performance, we empower employees to think like owners, giving them a stake in the organization.
All employees receive equity, which we believe reinforces our ownership culture. Base salary is determined by several factors including the candidate's qualifications, skills, education, experience, business needs and market demands. As of the date of this posting, a good faith estimate of the current pay scale for this position, applicable to all candidates, is $207,000 - $253,000 per year. We comply with all applicable minimum wage laws.
All full-time employees receive equity, which reinforces our ownership culture and offers meaningful opportunity for our employees to share in the success they help create. By aligning individual and company performance, we empower employees to think like owners, giving them a stake in the organization.
Full-time employees are also eligible for comprehensive benefits, including flexible paid time off, medical, dental, vision and life/disability insurance, and 401(k) offerings (i.e., traditional, Roth, and employer match) in accordance with applicable plans. We also offer additional voluntary benefits like supplemental life insurance, legal services, and other offerings. In addition, we offer mental health benefits through our Employee Assistance Program for employees and their family. The company also provides other benefits in accordance with applicable federal, state, and local laws.
We are committed to providing reasonable accommodations for individuals with disabilities throughout the hiring process. If you need assistance, please contact HR@madrigalpharma.com.
Madrigal is an Equal Opportunity Employer. All employment is decided on the basis of qualifications, merit, and business need. Applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex gender identity, sexual orientation, national origin, age, disability, protected veteran or disabled status, or other characteristic protected by applicable federal, state, or local law.
Unsolicited resumes from agencies should not be forwarded to Madrigal. Madrigal will not be responsible for any fees arising from the use of resumes through this source. Madrigal will only pay a fee to agencies if a formal agreement between Madrigal and the agency has been established.
Applications are being accepted on an ongoing basis and can be submitted through our Madrigal Careers site.
Please be aware that we have received reports of individuals misrepresenting themselves as Madrigal Pharmaceuticals' Hiring Managers, seeking to engage with job candidates through fraudulent online advertisements or job posting sites. These unauthorized individuals are using Madrigal's name and logo in an attempt to solicit up-front fees and obtain personal information from interested job candidates. Please know that Madrigal does not conduct interviews via text or in chat rooms; conduct interviews via Skype, RingCentral or solely via telephone; charge candidates an advance fee of any kind (e.g., fees for purchasing equipment); nor does it offer positions of employment without undergoing a thorough recruiting process.
Please also note that any correspondence with regard to employment would come from an authorized madrigalpharma.com email address or from an email address from one of our trusted search firm partners. We are aware that incorrect/fraudulent email addresses, with Madrigal misspelled, have been utilized in these most recent fraud attempts. If you receive unsolicited employment offers from people claiming to work for or on behalf of Madrigal, we recommend that you: do not respond to their questions; do not open any attachments; and do not click on any hyperlinks. Any questions regarding the legitimacy of job-related contacts can be directed to HR@madrigalpharma.com.
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Pharmaceutical and medicine manufacturing
11 - 50 Employees
Conshohocken, PA, US
2011