Lead regulatory strategy and execution for Mapp Biopharmaceutical’s product development programs, managing FDA interactions, submissions, and compliance across all disciplines.
Compensation
Mapp's anticipated pay scale for this position is $130,000 to $250,000, plus any applicable bonuses.
Responsibilities
Ensures that all regulatory goals are met and are in compliance with current industry standards and global regulations
Serves as a steward of Regulatory Affairs processes, procedures, and tools
Contributes to coordination, preparation, and timely submission of all regulatory documents
Develops regulatory strategies for the company and product development teams
Facilitates FDA interactions, presentations and negotiations
Requirements
Bachelor's degree in a related field
Advanced degree or equivalent preferred
Nice to have: Monoclonal antibody development
Nice to have: BLA submission
Nice to have: Commercialization of monoclonal antibody therapies
Lead and execute regulatory strategy for implantable neurostimulation therapy for obstructive sleep apnea, supporting global regulatory activities in the U.S. and EU.
Compensation
$110,000—$150,000 USD
Responsibilities
Serve as a strategic regulatory partner to cross‑functional teams
Assess regulatory impact for new product development and post‑market changes
Develop and communicate regulatory pathway options
Compile, prepare, review, and submit high‑quality regulatory submissions in the U.S. and EU
Collaborate with subject matter experts to respond to regulatory authority questions
Requirements
Bachelor's degree in engineering, life sciences, or related scientific discipline
Nice to have: medical device industry experience
Nice to have: quality
Nice to have: engineering
Nice to have: software regulated as a medical device
Lead medical and scientific strategy for immunology programs, partnering with business development, clinical operations, and regulatory teams to design and execute clinical programs and bid defenses.
Compensation
Expected Salary Range: $340,000 to $380,000 USD – Salary offered will be based on candidates experience level.
Responsibilities
Provide deep therapeutic and scientific leadership for protocol design and scientific advisory interactions
Serve as primary therapeutic and development expert for client-facing proposals, bid defenses, and early study concept development
Build and maintain relationships with clients, KOLs, principal investigators, and high-performing clinical sites
Support investigator identification and site selection strategies to optimize enrolment and data quality
Advise cross-functional teams on regulatory strategy, endpoint selection, safety monitoring and comparator standards
Requirements
Medical Doctor (MD) or equivalent medical degree in the United States
Advise on SEC and CFTC regulations for Kalshi’s products and help shape regulatory strategy as the company expands into new financial products and markets.
Compensation
Salary Range: $250,000–$300,000+ annually, plus equity and benefits.
Responsibilities
Advise on the application of SEC and CFTC regulations to Kalshi's existing and emerging products, businesses, and market infrastructure.
Help develop regulatory strategies for new financial products, including securities-linked derivatives and other innovative trading instruments.
Nscale's lead US regulatory and policy lawyer advising on legislative drafting, regulatory strategy for US campuses (site selection, energization, and operation), and engagement with federal and state regulators.
Compensation
$240,000—$420,000 USD
Responsibilities
Partner with Policy on advocacy around emerging GPU, large-load, co-location, and data center rulemakings at the federal and state level.
Help determine regulatory strategy for US campuses.
Manage strategy on contested permits.
Run regulatory due diligence on site acquisitions, power deals, and project-financed sites.
Partner with infrastructure, energy procurement, and construction counsel to ensure EPC, PPA, interconnection and O&M agreements reflect regulatory requirements.
Requirements
JD from an accredited US law school
active membership in good standing of at least one US state bar
Nice to have: In-house experience at a hyperscaler, neocloud, colocation provider, data center developer, utility, IPP or infrastructure investor
Nice to have: Experience with behind-the-meter or co-located generation (gas turbines, reciprocating engines, storage, or nuclear/SMR arrangements)
Nice to have: Experience leading regulatory work in Texas (ERCOT and PUCT) and PJM states
A strategic leadership role requiring deep experience in the energy regulatory landscape to shape, influence, and navigate the evolving state and federal policies that impact the business.
Responsibilities
Develop and lead a proactive policy agenda that supports organizational goals in energy, water use, conservation, and economic development.
Track, analyze, and communicate the impacts of federal and state legislation, regulations, and tax incentives on our operations.
Advocate for regulatory outcomes that align with strategic objectives, including accelerated interconnection, data center incentives, and broader energy policy outcomes.
Work closely with executive leadership—particularly with the Energy Origination, Tax, Finance, and Legal teams—to align policy priorities.
Serve as the primary liaison with federal agencies, Congressional offices, state regulatory commissions, and economic development committees.
Provides complex management, coordination, expertise and direction in the performance of regulatory activities, ensuring compliance with regulations and regulatory laws.
Compensation
$79,643 - $106,184
Responsibilities
Coordinate and monitor compliance issues for the organization
Oversee accurate and timely regulatory filings and reports to regulatory agencies
Research laws and regulations, investigate facts and prepare reports and documents pertaining to compliance issues
Manage the regulatory process to maintain compliance by working closely with inside and outside counsel and Business units
Prepare briefing material and/or communications for senior management, customer and client organizations and regulators
Lead cardiovascular medical science and strategy for PPD clinical research business, driving RFP quality, strategic alliances, and clinical development expertise.
Locations (2)
Raleigh, North Carolina, United States
United States
Compensation
Competitive salary and benefits
Responsibilities
Ensure high-quality input into RFPs including strategy, regulatory, drug class, protocol and safety considerations
Provide therapeutic and developmental expertise to internal teams and clients
Support bid defenses and client governance
Develop and review regulatory documents such as Investigator Brochure, NDA/MAA packages
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