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Every career with Hearst Television is like a story. How it develops, where it takes you, the milestones you reach along the way – you’ve got a lot to look forward to as your unique career story unfolds. Hearst Television, a subsidiary of Hearst, owns and operates local television and radio stations serving nearly three dozen U.S. cities, reaching 24 million U.S. television households. Through its partnership with nearly all major networks, Hearst Television distributes national content across more than 120 video channels, including programming from ABC, NBC, CBS, CW, MY Net, MeTV, This TV, Estrella, and more. Hearst Television is recognized as one of the industry's premier companies. It has been honored with numerous awards for distinguished journalism and industry innovation, including the Walter Cronkite Award for political journalism, the national Edward R. Murrow Award, the DuPont-Columbia Award, and the George Foster Peabody Award.

","New York, NY","coloredLogo","logoAttachment","Hearst.png","thumbnail","thumbnailAttachment","Hearst_TV_Careers.png","hexCode","#2D75B9","headline","National multimedia company reaching 24 million households","https://production-rails-default.s3.amazonaws.com/uploads/company/logo_attachment/1072/Hearst.png","/companies/hearst-television","https://production-rails-default.s3.amazonaws.com/uploads/company/thumbnail_attachment/1072/Hearst_TV_Careers.png","hasJobSubmission","isSavedJob","similarJobs",[512,521,531,540,554],{"_429":428,"_434":513,"_452":453,"_444":514,"_243":438,"_441":438,"_427":428,"_111":515,"_431":432,"_433":194,"_454":453,"_442":443,"_425":516,"_455":517,"_430":115,"_476":477,"_460":518,"_478":515,"_479":443,"_481":519,"_483":484,"_485":520},["D",1771372800000],"Structure Therapeutics","Director, Drug Product Development",["B","2619504256"],"Work at Structure Therapeutics","/jobs/2619504256-director-drug-product-development","/jobs?keyword=Structure+Therapeutics","/jobs?keyword=Director%2C+Drug+Product+Development",{"_429":428,"_434":522,"_452":453,"_444":523,"_243":438,"_441":438,"_427":428,"_111":524,"_431":432,"_433":194,"_454":453,"_442":443,"_425":525,"_455":526,"_430":115,"_476":527,"_460":528,"_478":524,"_479":443,"_481":529,"_483":484,"_485":530},["D",1771286400000],"Electra Therapeutics, Inc.","Director, GCP Quality Assurance",["B","2619502968"],"Work at Electra Therapeutics, Inc.","2 days ago","/jobs/2619502968-director-gcp-quality-assurance","/jobs?keyword=Electra+Therapeutics%2C+Inc.","/jobs?keyword=Director%2C+GCP+Quality+Assurance",{"_429":428,"_434":532,"_452":453,"_444":533,"_243":438,"_441":438,"_427":428,"_111":534,"_431":432,"_433":194,"_454":453,"_442":443,"_425":535,"_455":536,"_430":115,"_476":477,"_460":537,"_478":534,"_479":443,"_481":538,"_483":484,"_485":539},["D",1771372800000],"Pfizer","Director of Oncology Early Development",["B","2619523058"],"Work at Pfizer","/jobs/2619523058-director-of-oncology-early-development","/jobs?keyword=Pfizer","/jobs?keyword=Director+of+Oncology+Early+Development",{"_429":428,"_434":541,"_452":453,"_444":542,"_243":543,"_441":544,"_427":428,"_111":545,"_431":194,"_433":194,"_454":453,"_442":546,"_425":547,"_455":548,"_430":115,"_476":549,"_460":550,"_478":545,"_479":546,"_481":551,"_483":552,"_485":553},["D",1769446800000],"Denali Therapeutics","Neurodegenerative diseases are one of the largest medical challenges of our time. Denali Therapeutics is a biotechnology company dedicated to developing breakthrough therapies for neurodegenerative diseases through our deep commitment to degeneration biology and principles of translational medicine. Denali is founded on the collaboration of leading scientists, industry experts, and investors who share the vision that scientific discovery energetically applied to translational medicine is the key to delivering effective therapies to patients.\nWe invite you to consider an opportunity with Denali to help achieve our goal of delivering meaningful therapeutics to patients.

Key Accountabilities/Core Job Responsibilities

Act as \"thought partner,” to the CSO, discovery leadership, Early Denali Portfolio Leadership (DPL) and Cross-Functional Partners (e.g., Finance, HR) for both internal and external activities

Partner with Chief People Officer and General Counsel for business operations

Facilitate and manage a broad range of projects to help ensure attainment of strategic priorities consistent with corporate goals

Work with leadership team members individually and collectively on key business projects

Ensure that key initiatives in support of Denali’s goals are on track, intervening as appropriate to ensure meeting goals. Monitor and report progress to CSO, CTO, and GC, triaging and escalating issues as appropriate

Work with the leadership team and others to translate strategy into deliverables that can be measured and managed

Support the development and preparation of executive-level presentations

Identify and prioritize key issues early and expedite resolution by integrating information search, analysis and evaluation to provide an informed perspective and propose solutions

Effectively prioritize multiple objectives, monitor progress of ongoing activities and implement course corrections as needed using project management and business improvement capabilities

Organize and drive the rhythm of decision making and outputs to feed in to key meetings and initiatives

Track key initiatives by monitoring progress towards meeting goals, ensuring follow-through on the part of relevant players and sustaining momentum needed to drive these initiatives

Influence appropriate stakeholders and ensure appropriate prioritization and project management to support the business in meeting their objectives

Develop agendas, manage meeting flow, summarize and follow-up on actions to ensure timely execution

Draft and minute key discussion points for Discovery, Technical Operations, and Legal strategy meetings

Qualifications/Skills

BS/MS in a scientific discipline with life sciences experience preferred

7+ years of experience in project management

Proven experience in Knowledge Management, Communication, Strategy/Planning

Industry exp: Pharma, Biotech, Life Sciences

Advanced skills in Microsoft Office suite, particularly with PowerPoint and Excel

Can do attitude and analytic problem-solving skills

Ability to anticipate and remediate problems that arise

Strong interpersonal skills

Capable of conveying scientific information in a clear and thorough manner

Highly developed verbal and written communication skills, with a demonstrated ability to compose concise, sensitive and professional emails

Team oriented, highly motivated, execution focused with strong work ethic, ability to thrive in a high growth, collaborative, entrepreneurial environment

Highly adaptable and responsive to technical and business opportunities and needs – comfortable delivering against challenging commitments

Willingness to work hard and take direction and also anticipate problems and their solutions without explicit guidance

Salary Range: $0.00 to $0.00. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Denali offers a competitive total rewards package, which includes a 401k, healthcare coverage, ESPP and a broad range of other benefits. Learn more at https://www.denalitherapeutics.com/careers

This compensation and benefits information is based on Denali’s good faith estimate as of the date of publication and may be modified in the future. Denali is committed to its core company value of unity by creating a diverse and inclusive environment. We are proud to be an equal opportunity employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, basis of disability, or any other federal, state, or local protected class.

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Senior Director, Regulatory Affairs – Oncology Strategy

Pliant Therapeutics is a clinical‑stage biopharmaceutical company and leader in the discovery and development of novel integrin‑based therapeutics. Based in South San Francisco, California, Pliant was founded in 2015 to develop therapeutics to modulate specific pathways upregulated or dysfunctional in certain diseases. Our approach involves developing novel integrin‑based therapeutics to treat solid tumors and other diseases. Integrins are a crucial link between a cell’s internal structure and its external environment and function in cell signaling, regulation and adhesion as well as wound healing and immune response.

Founded by a team of world‑renowned researchers from the University of California, San Francisco, this group discovered key insights into the integrin biology and developed small molecule therapeutics to target this devastating disease process. Launched in 2016 by Third Rock Ventures, a leading healthcare venture capital firm, Pliant has developed an industry‑leading proprietary library of over 15,000 integrins that serve as a key driver to its portfolio. We believe our platform may be broadly applicable across multiple disease areas including delivery of drug payloads to cells utilizing integrin receptor‑binding molecules as tissue‑specific delivery and internalization mechanisms. Currently, Pliant is conducting a Phase 1 study of PLN‑ , a small molecule, dual‑selective inhibitor of αvβ8 and αvβ1 integrins, that has shown encouraging clinical activity in the development of a treatment of immune checkpoint‑resistant solid tumors.

Description

The Senior Director, Regulatory Affairs will report to the Vice President, Regulatory & Compliance and is responsible for leading, developing and executing the global regulatory strategy for Pliant’s oncology programs. This involves oversight for regulatory activities across the product lifecycle, from development through post‑approval, while overseeing department activities and representing Regulatory Affairs in cross‑functional teams. This highly visible and hands‑on role will provide both strategic and operational support to regulatory activities across multiple therapeutic areas. This person will also lead interactions with the FDA and other regulatory agencies.

The Senior Director, Regulatory Affairs, must have strong strategic regulatory experience in oncology and be able to provide sound guidance, communicate clearly (in verbal and written form), and display exemplary organizational / leadership skills. In addition, the Senior Director, Regulatory Affairs, will support an environment in which the team is highly motivated and engaged to work collaboratively within their team as well as cross‑functionally to deliver exceptional results and ensure long‑term success.

Responsibilities

Lead the development and implementation of regulatory oncology strategies that result in successful registration and post‑approval commercialization of products and product‑candidates.
Provide guidance to the cross‑functional teams based on technical and regulatory knowledge toward the development and implementation of strategic and tactical plans in alignment with corporate objectives.
Proactively identify and assess regulatory risks associated with product development for Pliant’s oncology program.
Serve as the regulatory agency contact (e.g. FDA and other agencies) and in this capacity, foster strong agency relationships while acting as a credible, reputable, and effective advocate for the company.
Effectively lead meetings with Health Authorities to ensure full resolution of issues and opportunities.
Lead all interactions/submissions to global Health Authorities including initial IND/CTAs, NDA/MAAs, supplements and variations, and any other key areas of discussions.
Ensure the regulatory strategy is aligned with global Health Authority requirements and review documents for submission readiness to ensure that all submissions conform to relevant guidelines.
Ensure that content in regulatory applications is complete, well‑written, and meets all relevant requirements for the program’s development phase.
Support the product team in managing and directing regulatory inspections.
Keep peers and superiors apprised of expected changes to the regulatory landscape affecting existing and future products and provide strategic and tactical direction to drive cross‑discipline consistency in regulatory approach and planning.
Facilitate the strategies for the approval of products in rest‑of‑world regions either by the company or by its partners/affiliates, and act as the regulatory contact for ongoing alliance management activities.
Partner with and support clinical development, CMC, medical affairs, commercial and corporate activities, including the review and submission of clinical protocols and regulatory documents, publications, investor relations/legal public disclosures throughout the product life cycle.
Support the Pharmacovigilance and Safety functions as an active member of the Safety Governance and Review team.
Lead, manage, and develop a high performing team to support organizational growth as a late‑stage clinical organization, including providing professional and personal growth opportunities, mentorship, and change management.
Provide the business development team with guidance and critical evaluation of potential product opportunities, in support of strategic partnering and licensing activities.
Support long and short‑term departmental planning including structure, headcount, budgeting, training, and systems requirements.
Help manage the external regulatory vendor and service team members and providers.
Manage internal regulatory procedures to ensure compliance.

Qualifications

BA/BS Degree required in a health/life sciences or related field. Advanced degree preferred.
A minimum of 15 years in Regulatory Affairs, of which at least 8 years have been in oncology and at least 6 years of leadership experience managing a team.
Direct and successful experience in Regulatory activities including IND/CTA, NDA/BLA/MAA, lifecycle management, and developing and implementing complex regulatory strategies.
Proven experience leading interactions and negotiations with Health Authorities (US and ex‑US preferred).
Strong understanding of relevant US FDA regulations as well as international regulatory agencies (e.g. EU/EMA).
Experience in the ability to deliver high quality regulatory submission documents.
Strong strategic skills including demonstrated ability to make complex decisions and willingness to defend difficult positions.
Proven success in simultaneously handling strategic and transactional responsibilities, especially in a small‑team environment.
Demonstrated excellence in project management with a proven track record of effectively managing multiple projects / priorities simultaneously.
Exceptional written and oral communication skills.
Excellent interpersonal skills with ability to lead, interact with, focus, resolve conflict and drive consensus among individuals from a variety of cultures, and disciplines.
Managerial and personal development experience required.

How you work

Dare to Succeed: Approach regulatory strategy with courage and creativity, challenging convention when it advances patient outcomes. Take ownership of ambitious goals and navigate early‑development ambiguity with resilience and sound judgment.
Make an Impact: Operate with urgency and focus, prioritizing high‑value actions that drive programs forward. Elevate regulatory quality and efficiency by anticipating obstacles and building scalable, best‑in‑class processes.
One Pliant: Collaborate seamlessly across functions, building trust and alignment with internal and external partners.

Compensation

The annual base salary for this role is $270K – $300K. Individual pay may vary based on additional factors, including, and without limitation job‑related skills, experience, work location and relevant education or training. Pliant’s compensation package also includes benefits, equity, and an annual target bonus for full‑time positions.

Equal Opportunity Employer

We do not discriminate on the basis of any protected group status under any applicable law.

#J-18808-Ljbffr","

Senior Director, Regulatory Affairs – Oncology Strategy

Pliant Therapeutics is a clinical‑stage biopharmaceutical company and leader...","Senior Director, Regulatory Affairs – Oncology Strategy South San Francisco, CA",["B","2628501131"],"Work at Pliantrx","1 hours ago","/jobs/2628501131-senior-director-regulatory-affairs-oncology-strategy-south-san-francisco-ca","Senior Director, Regulatory Affairs – Oncology Strategy South San...","/jobs?keyword=Pliantrx","/jobs?location=South+San+Francisco","/jobs?keyword=Senior+Director%2C+Regulatory+Affairs+%E2%80%93+Oncology+Strategy+South+San...","actionData","errors"]