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Frontier Medicines information

What is the difference between Frontier Medicines vs Clinical Research Associate?

AspectFrontier MedicinesClinical Research Associate
Primary RoleDevelops and researches new medicines and therapies in a biotech or pharmaceutical settingMonitors clinical trials to ensure compliance and data integrity
Required CredentialsTypically requires a degree in life sciences, pharmacology, or related fields; certifications varyRequires a degree in life sciences or healthcare; often requires GCP certification
Work EnvironmentLaboratories, research facilities, biotech companiesClinical trial sites, hospitals, research organizations
Industry UsageBiotech and pharmaceutical R&DClinical trial management and monitoring

Frontier Medicines focuses on developing new drugs and therapies within biotech and pharmaceutical research, while Clinical Research Associates primarily oversee and monitor clinical trials to ensure compliance and data quality. Both roles require a background in life sciences and are integral to the drug development process, but they differ in daily responsibilities and work environments.

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Infographic showing various Frontier Medicines job openings in the United States as of August 2026, with employment types broken down into 3% Internship, 89% Full Time, 6% Part Time, 1% Contract, and 1% Nights. Highlights an 85% Physical, 3% Hybrid, and 12% Remote job distribution.

Associate Director, Strategy & Operations, Genetic Medicines

Regeneron Pharmaceuticals, Inc (USA)

Tarrytown, NY • On-site

$157.20 - $256.60/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 18 days ago


Regeneron rating

8.4

Company rating: 8.4 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

22nd of 86 rated pharmaceutical


Job description

Build our future together: At Regeneron, we use science and innovation to develop life‑changing medicines for people with serious diseases. We are seeking an Associate Director to join our Regeneron Genetic Medicines Clinical Development Unit (RGM CDU). The Associate Director Strategy Planning & Operations reports to and works closely with the RGM CDU Leadership Team (LT) in support of the operational management of the department. The scope of this role includes supporting departmental meetings, objective and goal setting, support of cross‑functional projects, review and tracking of RGM CDU top deliverables, headcount and resource forecasting, and team communications. The role also supports initiatives to establish a high‑performing, strategic, effective, and quality‑focused organization that is well‑aligned and integrated with other functions, including RGM research, the Regeneron Genetic Center (RGC), and Global Development. A key expectation of this role is the active adoption and promotion of AI‑powered productivity tools to elevate quality, speed, and impact of strategic work across the organization.

Location & Work Format

Location: Tarrytown, NY
Hybrid: 4 days per week on site

Role Overview

The position offers the opportunity to contribute to a fast‑growing, science‑driven organization making a meaningful difference to patients worldwide.

Key Responsibilities
  • Act as a strategic partner across the RGM CDU Leadership Team and the broader organization, driving alignment in support of portfolio and departmental planning with an emphasis on long‑term strategic objectives.
  • Oversee the collation and tracking of critical program and departmental initiatives, ensuring alignment with organizational goals.
  • Lead cross‑functional strategic initiatives, special projects, and organizational planning efforts to foster collaboration and innovation.
  • Develop and deliver high‑impact presentations for the Head of the RGM CDU covering pipeline progress, strategic issues, RGM overviews for external collaborators, financial performance updates, and organizational changes.
  • Enhance resource management strategies.
  • Engage in strategic mid‑range planning for headcount needs, encompassing both permanent and contract staff, while proactively managing the approval process for permanent headcount.
  • Guide RGM line managers in performance and talent management discussions, partnering with functional leaders to refine succession planning processes.
  • Spearhead infrastructure and space planning initiatives, developing strategic recommendations for changes in collaboration with the RGM CDU LT to optimize operational efficiency.
  • Lead the preparation and facilitation of monthly departmental meetings, including strategic planning, communications, agenda development, and comprehensive minutes distribution to ensure accountability and follow‑up on key action items.
  • Identify and champion opportunities for continuous improvement, proposing innovative solutions to enhance operational efficiencies through regular engagement with RGM CDU & ES LT and their teams.
  • Collaborate extensively with Global Development Strategic Planning & Operations personnel to navigate process changes and address issues impacting RGM CDU and Global Development, ensuring alignment with broader organizational strategies.
  • Champion the adoption of AI productivity tools (e.g., Claude, Microsoft Pilot, Copilot) across RGM CDU to streamline operational workflows, accelerate document and presentation development, synthesize complex information, and enhance strategic output.
Qualifications
  • Bachelor’s degree and 10+ years of experience required; MBA, PhD, Pharm D preferred.
  • Demonstrated depth of understanding of the drug development process.
  • Agile problem solver with strong planning ability, interpersonal and communication skills, along with scientific and business acumen.
  • Demonstrated proficiency in AI‑powered productivity tools with a track record of applying them to accelerate knowledge work.
  • Comfort operating at the frontier of AI tool adoption, with curiosity and initiative to identify new applications, evaluate emerging tools, and guide others in their use.
  • Highly organized and detail‑oriented, demonstrating ability to synthesize information and think strategically.
  • Self‑motivated, flexible, proactive, able to follow through in an ambiguous, fast‑changing environment.
  • Ability to prioritize and manage multiple projects simultaneously.
  • Experience contributing or leading cross‑functional strategic change initiatives.
  • Expertise in MS applications (TEAMS, Project, PowerPoint, Word, Excel).
Benefits
  • Annual bonuses or other incentive plans.
  • Equity awards.
  • Pension or retirement benefits.
  • 401(k) company match.
  • Health and wellness programs.
  • Insurance benefits (medical, dental, vision, life, disability).
  • Paid time off.
  • Family support benefits.
Salary Range

Annually: $157,200.00 - $256,600.00

EEO Statement

We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship. Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits.

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