1,003 Results for

Assistant Jobs in Palatine, IL

Jobs

Senior Regulatory Affairs Specialist - Software OrganOx

Madison, NJ

$115,000–$140,000 / year
Quick Apply

Under direction from the Director, Regulatory Affairs, Software and Innovation, the Senior Regulatory Affairs Specialist will be responsible for: · Providing regulatory affairs support for projects related to Digital Health, Software, Cybersecurity, Electromechanical devices and Regulatory Intelligence. Founded in 1921, Terumo Corporation strives to fulfill its mission of “Contributing to Society through Healthcare” by providing a comprehensive range of solutions in the fields of therapeutic procedures, hospital operations, and life sciences in more than 160 countries and regions.

30+ days ago

Regulatory Affairs Strategist, Globalization (Americas - US, Canada, LATAM) Becton Dickinson and Co

Franklin Lakes, NJ

$137,500–$220,100 / year

The Regulatory Affairs Strategist, Globalization, is responsible for implementation of worldwide regulatory affairs strategies and practices related to their assigned area of focus and expertise across the BU, Regional and Central teams. Act as a strategic partner to Business Units and Regional Regulatory leaders, enabling aligned execution of regulatory strategies through tools, processes, and best‑practice sharing.

30+ days ago

Associate Director, Regulatory Affairs (CMC) Insmed Inc

Bridgewater, NJ

Remote

$164,000–$213,000 / year

Reporting to the Senior Director, Regulatory Affairs CMC, EMEA, you'll have responsibility for leading CMC regulatory strategy development and implementation that incorporates risk identification and mitigation for assigned development and post approval programs to achieve regulatory approvals in the EMEA region. As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, you'll be part of a community that prioritizes the human experience, celebrates curiosity, and values every person's contributions to meaningful progress.

30+ days ago

Director/Sr. Director/Executive Director, Clinical Regulatory Affairs SystImmune, Inc.

Princeton, NJ

$200,000–$300,000 / year

The Regulatory Affairs (Clinical/Nonclinical) role will drive regulatory strategy and execution within SI Project development teams and the RA Department in all aspects of global regulatory affairs related to development of novel oncology therapeutics (multiple modalities such as ADCs, bispecific antibodies and T-cell engagers etc.). Own/drive the preparation, submission, management and maintenance of global regulatory submissions related to clinical and nonclinical aspects of product development, including, but not limited to, the following: BLA/INDs/CTAs, amendments and information requests, Orphan drug applications, Annual Reports and Investigator's Brochure.

30+ days ago

Sr. Director/Executive Director, Regulatory Affairs SystImmune, Inc.

Princeton, NJ

$220,000–$300,000 / year

4 days ago

Senior Manager / Associate Director, Regulatory Affairs CMC Shionogi & Co Ltd

Florham Park, NJ

$140,000–$200,000 / year

Serve as the primary CMC regulatory liaison with Health Authorities for designated assets, which involves guiding agency communications, creating briefing documents, handling information requests, and ensuring alignment with management on strategic or high‑risk issues before making commitments. Excellent verbal communication skills, with demonstrated ability to act as a regulatory CMC spokesperson and effectively communicate aligned regulatory CMC strategies and positions across working teams, cross‑functional forums, and senior leadership.

30+ days ago

Sr. Director, Regulatory Affairs Eikon Therapeutics, Inc.

Jersey City, NJ

$235,000–$288,750 / year

This role will require a minimum of 3 days a week of onsite presence (or more as business needs require) in our Jersey City (NJ) office to ensure effective management, operational excellence and high-performance delivery of clinical studies and to support the expected significant team growth & collaboration. In this role, they will excel in developing and executing regulatory strategies, ensuring compliance, managing submissions, fostering cross-functional collaboration, liaising with regulatory agencies, supervising quality assurance, and addressing regulatory risks associated with projects.

30+ days ago

Senior Associate, Regulatory Affairs Submission Management - Hybrid AbbVie

Florham Park, New Jersey

$84,500–$162,000
Full time

With input from the submission teams, this individual establishes and maintains submission content planners and associated timelines, facilitates tactical submission team meetings, prepares content planners for publishing, interfaces with publishing vendor, and fulfills Submission Management functions on Project Teams in support of Development, Marketing, and post-marketing regulatory authority applications. Manages medium to high impact (with respect to internal visibility, risk, complexity and criticality) submission projects to ensure the timely delivery of high-quality dossiers that meet technical specifications defined by regulatory authorities and can be easily navigated and reviewed by a regulatory agency.

3 days ago

Senior Associate Regulatory Affairs Submission Management - Hybrid AbbVie Inc

Florham Park, NJ

With input from the submission teams, this individual establishes and maintains submission content planners and associated timelines, facilitates tactical submission team meetings, prepares content planners for publishing, interfaces with publishing vendor, and fulfills Submission Management functions on Project Teams in support of Development, Marketing, and post-marketing regulatory authority applications. Responsibilities: Manages medium to high impact (with respect to internal visibility, risk, complexity and criticality) submission projects to ensure the timely delivery of high-quality dossiers that meet technical specifications defined by regulatory authorities and can be easily navigated and reviewed by a regulatory agency.

2 days ago

Regulatory Affairs II #1760 Enhanced Compliance Inc.

Parsippany, NJ

Full time

Supporting basic and advanced market entrance, providing acquisition due diligence, UDIs, and clinical evaluation reporting (CERs) Supports regulatory compliance activities, including processing of complaints and submitting Medical Device Reports and Vigilance Reports Assists in CE Marking activities, including preparation of Clinical Evaluation Reports, Technical Files and Design Dossiers Represents regulatory function on cross-functional product development and manufacturing support teams. Anticipate regulatory obstacles and emerging issues throughout the product lifecycle and develop solutions with other members of regulatory and related teams Interact with European Authorized Representative Interact with country regulatory authorities as needed Assists in special projects as needed.

5 days ago

Senior Manager Regulatory Affairs Global Reg Strategy US & Canada AbbVie Inc

Florham Park, NJ

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.

20 days ago

2027 Future Talent Program - Global Regulatory Affairs - Oncology - Co-op Merck & Co Inc

Rahway, NJ

Required Skills: Clinical Research, Cloud Data Catalog, Collaboration, Critical Thinking, Data Analysis, Database Management, Data Science, Data Security, Leading Project Teams, Life Science, Pharmaceutics, Regulatory Affairs Management, Regulatory Management, Regulatory Processes, Regulatory Reporting, Regulatory Submissions, Scientific Writing. Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities.

30+ days ago

Director, Regulatory Affairs Strategy Judge Group

Warren, NJ

$190,000–$220,000 / year
Quick Apply

This individual serves as the regulatory affairs main contact to project teams, providing leadership across functions for regulatory strategic planning and execution related to achieving program milestones. By providing your phone number, you consent to: (1) receive automated text messages and calls from the Judge Group, Inc. and its affiliates (collectively "Judge") to such phone number regarding job opportunities, your job application, and for other related purposes.

30+ days ago

Regulatory Affairs Coordinator Capital Health

Hopewell, New Jersey

Reporting to the Manager of Regulatory Affairs, coordinates organization-wide as well as program-specific activities related to the regulatory process and the respective governing bodies, including NJ Department of Health, Centers for Medicare and Medicaid Services (CMS), DNV and others. When determining base salary and/or rate, several factors may be considered including, but not limited to location, years of relevant experience, education, credentials, negotiated contracts, budget, market data, and internal equity.

30+ days ago

Senior Regulatory Affairs Specialist OrganOx

Madison, NJ

$120,000–$137,000 / year
Quick Apply

It has been utilized in over 7,000 liver transplants to date to keep donor livers in a metabolically active state outside the body enabling longer preservation times and functional assessment of the organ prior to transplant, leading to an increased number of organs available for transplant. Founded in 1921, Terumo Corporation (TSE:4543) strives to fulfill its mission of “Contributing to Society through Healthcare” by providing a comprehensive range of solutions in the fields of therapeutic procedures, hospital operations, and life sciences in more than 160 countries and regions.

30+ days ago

2027 Co-Op: Regulatory Affairs (6 months, Jan. start) GSK

Warren, New Jersey

Please include the following in your email: Use subject line: ‘Haleon Careers: Job Accommodation Request’ Your Name and contact information Requisition ID and Job Title you are interested in Location of Requisition (city/state or province/country) Description of specific accommodation you are requesting Please note: Resumes, CVs, or other requests outside of accommodation support submitted to this email box will not be accepted. Currently enrolled in a Bachelor's degree program in Life Sciences, Biology, Chemistry, Pharmacy, Public Health, Health Sciences, Regulatory Science, or a related field, graduating between December 2027 and May 2028.

24 days ago

2027 Co-Op: Regulatory Affairs (6 months, Jan. start) Haleon Plc

Warren, NJ

Currently enrolled in a Bachelor's degree program in Life Sciences, Biology, Chemistry, Pharmacy, Public Health, Health Sciences, Regulatory Science, or a related field, graduating between December 2027 and May 2028. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, Haleon may be required to capture and report expenses Haleon incurs, on your behalf, in the event you are afforded an interview for employment.

25 days ago

Legal Counsel Of Corporate And Regulatory Affairs Atlantic Health System

Morristown, NJ

Draft, review, negotiate, and interpret a broad range of commercial agreements, including professional services agreements, physician and provider arrangements, purchasing and supply chain contracts, consulting agreements, confidentiality agreements, technology and software agreements, revenue-generating partnerships, and other operational contracts. As a member of a collaborative in-house legal department, Counsel will work closely with executive leadership, clinical and operational teams, compliance professionals, and business partners to develop practical legal solutions that advance innovation while ensuring regulatory compliance and protecting the organization's mission.

30+ days ago

Legal Counsel of Corporate and Regulatory Affairs Atlantic Health System Inc

Morristown, NJ

30+ days ago

Regulatory Affairs Compliance Manager PBF Energy Inc

Parsippany, NJ

$106,787.51–$189,503.19 / year

This role includes day-to-day management of ISCC program requirements and risk management, continuous monitoring of regulatory and system updates, and direct accountability for mass balance, conversion factors, GHG calculations, and audit readiness and execution. Factors such as scope and responsibilities of the position, candidate's work experience, education/training, job-related skills and internal peer equity will be considered in determining the selected candidate's compensation.

30+ days ago

See More Jobs

Browse All Assistant Locations

Browse Jobs Near Palatine, IL

Get noticed by top employers!

Upload your resume to let employers know you're open to Assistant job opportunities. Plus, receive relevant job recommendations in your inbox.

Create A Free Account

Assistant Jobs in Palatine, IL

Senior Regulatory Affairs Specialist - Software OrganOx

Regulatory Affairs Strategist, Globalization (Americas - US, Canada, LATAM) Becton Dickinson and Co

Associate Director, Regulatory Affairs (CMC) Insmed Inc

Director/Sr. Director/Executive Director, Clinical Regulatory Affairs SystImmune, Inc.

Sr. Director/Executive Director, Regulatory Affairs SystImmune, Inc.

Senior Manager / Associate Director, Regulatory Affairs CMC Shionogi & Co Ltd

Sr. Director, Regulatory Affairs Eikon Therapeutics, Inc.

Senior Associate, Regulatory Affairs Submission Management - Hybrid AbbVie

Senior Associate Regulatory Affairs Submission Management - Hybrid AbbVie Inc

Regulatory Affairs II #1760 Enhanced Compliance Inc.

Senior Manager Regulatory Affairs Global Reg Strategy US & Canada AbbVie Inc

2027 Future Talent Program - Global Regulatory Affairs - Oncology - Co-op Merck & Co Inc

Director, Regulatory Affairs Strategy Judge Group

Regulatory Affairs Coordinator Capital Health

Senior Regulatory Affairs Specialist OrganOx

2027 Co-Op: Regulatory Affairs (6 months, Jan. start) GSK

2027 Co-Op: Regulatory Affairs (6 months, Jan. start) Haleon Plc

Legal Counsel Of Corporate And Regulatory Affairs Atlantic Health System

Legal Counsel of Corporate and Regulatory Affairs Atlantic Health System Inc

Regulatory Affairs Compliance Manager PBF Energy Inc

Similar Job Searches

See More Jobs