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Director, Regulatory Strategy

Hbap Fa Us1 Oraclecloud Com CX 1 · Waltham, MA, United States · Remote · Active · $208,000–$245,000 / week · Oracle Recruiting Cloud / Fusion HCM

Job facts

FieldValue
CompanyHbap Fa Us1 Oraclecloud Com CX 1
TitleDirector, Regulatory Strategy
Normalized title-
Department / teamResearch and Development
LocationWaltham, MA, United States
Work modelRemote / Remote
Employment typeFull Time
Salary$208,000–$245,000 / week
Statusactive
ATS providerOracle Recruiting Cloud / Fusion HCM
Posted / first seen2026-05-05 / 2026-05-31
Changed / last seen2026-05-31 / 2026-06-04

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Linked records

CompanyHbap Fa Us1 Oraclecloud Com CX 1
Sourcec9a1af55-d1aa-41d7-bb8e-0bf8dc082d85
ATS providerOracle Recruiting Cloud / Fusion HCM

Description

Description We are seeking an individual who is talented, motivated, and passionate about science to join our Regulatory Strategy team. As a Director of Regulatory Affairs, the successful candidate will play an important role in guiding new products into the clinic and setting the stage for registration. The individual in this role will serve as a Regulatory Lead for pipeline drug development programs and marketed products, and will be responsible for developing, implementing, and driving global Regulatory strategies. The ideal candidate will have a strong scientific background, broad experience developing drugs, and the ability to leverage that experience to impact program teams beyond regulatory strategy. This role reports to the Sr Director, Regulatory Affairs (Strategy) Responsibilities Serve as Regulatory Lead, representing the Global Regulatory Team on cross-functional development teams Develop and implement global regulatory strategies for pipeline drug development programs and marketed products Identify innovative, data-driven regulatory approaches, define plans to proactively mitigate risks, and monitor the competitive and policy landscape for changes with potential impact Lead the organization and preparation of clear and effective regulatory submissions that align with company strategies and Health Authority requirements Foster strong relationships with relevant regulatory agencies and key stakeholders while advocating for company positions Lead interactions with Health Authorities, interpret feedback, and ensure that the outcome is properly communicated to the Organization. Create a strong regulatory community and share best practices across the broader Regulatory Affairs organization Effectively represent the Regulatory Affairs function to senior leadership at governance meetings Qualifications Bachelor's degree in life sciences is required; advanced degree preferred At least 10 years’ experience in the biopharma industry in a Regulatory Lead role Preferred Requirements: Proven ability to represent Regulatory on project teams and at Health Authority meetings Demonstrated strategic thinking skills, sound judgement, and ability to integrate strategies into actionable plans Strong knowledge of global regulatory principles and practices across the drug development lifecycle, ideally with an emphasis on neurology drugs A thorough understanding of the drug development process and working knowledge of the essential activities for all key functional areas Excellent oral and written communication skills; solid grasp of effective regulatory writing fundamentals and ability to communicate complex issues clearly and concisely Strong team player: the ability to work flexibly in a collaborative environment and assist team members as needed to achieve goals Capable of project managing regulatory workstreams, identifying the critical path for submissions, and partnering with functional leads to manage timeline risk Able to work independently on competing priorities in a fast-paced and dynamic environment; a creative thinker with good attention to detail Alkermes has adopted a hybrid working environment to support and meet the needs of employees and this role will operate in a flexible environment with 60% of time in the office and 40% from home. This position is eligible for the hybrid workplace model, requiring work to be completed onsite at our Waltham, MA office at least 3 days per week. This role is not eligible for fully remote work. The annual base salary for this position ranges from $208,000 – $245,000. In addition, this position is eligible for an annual performance pay bonus. Exact compensation may vary based on skills, training, knowledge, and experience. Alkermes offers a competitive benefits package. Additional details can be found on our careers website: www.alkermes.com/careers#working-here Company Why join Team Alkermes? Alkermes applies its decades of deep neuroscience expertise to develop medicines designed to help people living with complex and difficult-to-treat psychiatric and neurological disorders. A global biopharmaceutical company, headquartered in Ireland with U.S. locations in Massachusetts and Ohio, we seek to make a meaningful difference in the way people manage their diseases. We have a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia, bipolar I disorder and narcolepsy, and a pipeline of clinical and preclinical candidates in development for various psychiatric and neurological disorders. We are proud to have been recognized as an employer of choice by many national organizations. In 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts’ Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine. Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any qualified applicant or employee because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, gender expression and identity, disability, genetic information, veteran status, military status, application for military service or any other characteristic protected by local, state or federal law. Alkermes also complies with all work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Alkermes is an E-Verify employer.

Full job record

Job ID791a07350a74ea770a5da805909dfc73440ca8b5
Org IDd831e3c2-6a79-44af-a2cf-903b76ab4731
Source IDc9a1af55-d1aa-41d7-bb8e-0bf8dc082d85
Board IDc9a1af55-d1aa-41d7-bb8e-0bf8dc082d85
Provideroracle_hcm
Provider Job Key13918
TitleDirector, Regulatory Strategy
Normalized Title—
Statusactive
Activeyes
Location TextWaltham, MA, United States
DepartmentResearch and Development
Team—
Employment Typefull_time
Workplace Typeremote
Remote Policyremote
CountryUnited States
RegionMA
CityWaltham
Salary RawDescription We are seeking an individual who is talented, motivated, and passionate about science to join our Regulatory Strategy team. As a Director of Regulatory Affairs, the successful candidate will play an important role in guiding new products into the clinic and setting the stage for registration. The individual in this role will serve as a Regulatory Lead for pipeline drug development programs and marketed products, and will be responsible for developing, implementing, and driving global Regulatory strategies. The ideal candidate will have a strong scientific background, broad experience developing drugs, and the ability to leverage that experience to impact program teams beyond regulatory strategy. This role reports to the Sr Director, Regulatory Affairs (Strategy) Responsibilities Serve as Regulatory Lead, representing the Global Regulatory Team on cross-functional development teams Develop and implement global regulatory strategies for pipeline drug development programs and marketed products Identify innovative, data-driven regulatory approaches, define plans to proactively mitigate risks, and monitor the competitive and policy landscape for changes with potential impact Lead the organization and preparation of clear and effective regulatory submissions that align with company strategies and Health Authority requirements Foster strong relationships with relevant regulatory agencies and key stakeholders while advocating for company positions Lead interactions with Health Authorities, interpret feedback, and ensure that the outcome is properly communicated to the Organization. Create a strong regulatory community and share best practices across the broader Regulatory Affairs organization Effectively represent the Regulatory Affairs function to senior leadership at governance meetings Qualifications Bachelor's degree in life sciences is required; advanced degree preferred At least 10 years’ experience in the biopharma industry in a Regulatory Lead role Preferred Requirements: Proven ability to represent Regulatory on project teams and at Health Authority meetings Demonstrated strategic thinking skills, sound judgement, and ability to integrate strategies into actionable plans Strong knowledge of global regulatory principles and practices across the drug development lifecycle, ideally with an emphasis on neurology drugs A thorough understanding of the drug development process and working knowledge of the essential activities for all key functional areas Excellent oral and written communication skills; solid grasp of effective regulatory writing fundamentals and ability to communicate complex issues clearly and concisely Strong team player: the ability to work flexibly in a collaborative environment and assist team members as needed to achieve goals Capable of project managing regulatory workstreams, identifying the critical path for submissions, and partnering with functional leads to manage timeline risk Able to work independently on competing priorities in a fast-paced and dynamic environment; a creative thinker with good attention to detail Alkermes has adopted a hybrid working environment to support and meet the needs of employees and this role will operate in a flexible environment with 60% of time in the office and 40% from home. This position is eligible for the hybrid workplace model, requiring work to be completed onsite at our Waltham, MA office at least 3 days per week. This role is not eligible for fully remote work. The annual base salary for this position ranges from $208,000 – $245,000. In addition, this position is eligible for an annual performance pay bonus. Exact compensation may vary based on skills, training, knowledge, and experience. Alkermes offers a competitive benefits package. Additional details can be found on our careers website: www.alkermes.com/careers#working-here Company Why join Team Alkermes? Alkermes applies its decades of deep neuroscience expertise to develop medicines designed to help people living with complex and difficult-to-treat psychiatric and neurological disorders. A global biopharmaceutical company, headquartered in Ireland with U.S. locations in Massachusetts and Ohio, we seek to make a meaningful difference in the way people manage their diseases. We have a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia, bipolar I disorder and narcolepsy, and a pipeline of clinical and preclinical candidates in development for various psychiatric and neurological disorders. We are proud to have been recognized as an employer of choice by many national organizations. In 2024 and 2025, we were certified as a Great Place to Work in the U.S. and named one of Massachusetts’ Top Places to Work by the Boston Globe, a Best Place to Work in Greater Cincinnati by the Cincinnati Business Courier and recognized as a Best Place to Work in BioPharma by Fortune Magazine. Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any qualified applicant or employee because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, gender expression and identity, disability, genetic information, veteran status, military status, application for military service or any other characteristic protected by local, state or federal law. Alkermes also complies with all work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Alkermes is an E-Verify employer.
Salary Min208,000
Salary Max245,000
Salary CurrencyUSD
Salary Periodweek
Source URLhttps://hbap.fa.us1.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/13918
Apply URLhttps://hbap.fa.us1.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_1/job/13918
First Seen At2026-05-31 18:10:58Z
Last Seen At2026-06-04 10:51:48Z
Last Checked At2026-06-04 10:51:48Z
Last Changed At2026-05-31 18:10:58Z
Inactive At—
Source Posted At2026-05-05 15:42:10Z
Source Updated At—
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    "BusinessUnitId": 100000000170392,
    "OrganizationId": 300000155417114,
    "PostingEndDate": null,
    "LegalEmployerId": 300000001067001,
    "PrimaryLocation": "Waltham, MA, United States",
    "WorkDurationYears": null,
    "WorkplaceTypeCode": null,
    "BeFirstToApplyFlag": false,
    "WorkDurationMonths": null,
    "otherWorkLocations": [],
    "secondaryLocations": [],
    "ShortDescriptionStr": "",
    "requisitionFlexFields": [],
    "DomesticTravelRequired": null,
    "PrimaryLocationCountry": "US",
    "ExternalQualificationsStr": null,
    "ExternalResponsibilitiesStr": null,
    "InternationalTravelRequired": null
  },
  "detail_meta": {
    "url": "https://hbap.fa.us1.oraclecloud.com/hcmRestApi/resources/latest/recruitingCEJobRequisitionDetails?expand=all&onlyData=true&finder=ById;Id=%2213918%22,siteNumber=CX_1",
    "http_status": 200,
    "content_type": "application/json",
    "response_bytes": 16479
  },
  "detail_errors": []
}
Get this page with API

Rendered from the bluedoor Job Postings API. Reproduce it:

GET https://api.bluedoor.sh/job-postings/v1/jobs/791a07350a74ea770a5da805909dfc73440ca8b5?include=descriptionJSON
GET https://api.bluedoor.sh/job-postings/v1/orgs/d831e3c2-6a79-44af-a2cf-903b76ab4731JSON
GET https://api.bluedoor.sh/job-postings/v1/sources/c9a1af55-d1aa-41d7-bb8e-0bf8dc082d85JSON
GET https://api.bluedoor.sh/job-postings/v1/jobs/791a07350a74ea770a5da805909dfc73440ca8b5/eventsJSON

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