Regulatory Affairs Associate I
$34 - $38 per hourCollabera
Pay Range $34.00/hr - $38.00/hr Location: Florham Park, NJ 07932 (100% Onsite) Duration: 12-Month Contract (Extension Based on Performance & Budget) Shift: Monday - Friday Contact: View email address on click.appcast.io (No C2C/Vendors) Position Details Industry: Pharmaceutical Job Title: Regulatory Affairs Associate I - Submission Management Pay Range: $34.00 to $35.00 per hour Purpose The Regulatory Affairs Associate I - Submission Management supports regulatory submission activities by managing low- to medium-impact regulatory submission projects. This role is responsible for coordinating submission content, maintaining submission timelines, supporting publishing activities, and ensuring submissions meet regulatory authority technical and quality standards. The position works cross-functionally with Regulatory Affairs, Development, Marketing, and post‑marketing teams to support global regulatory applications. Experience & Education Bachelor’s Degree required Minimum of 2 years of pharmaceutical or industry‑related experience Higher education may compensate for years of experience Years of experience may compensate for lower education Required Experience 2+ years of experience in the pharmaceutical or related regulated industry Experience supporting regulatory submission activities Experience coordinating cross‑functional teams and timelines Ability to manage multiple concurrent submission projects Familiarity with regulatory submission standards and health authority requirements Experience performing quality reviews of regulatory documents Preferred Experience Experience with publishing‑related software tools, including Documentum eCTDXPress / ISI Publisher ISI Toolbox DocuBridge / Insight Platform Adobe Acrobat Experience interfacing with submission publishing vendors Experience supporting eCTD submissions Responsibilities Manage low- to medium‑impact regulatory submission projects to ensure timely delivery of high‑quality dossiers. Establish, maintain, and track submission content planners and associated timelines. Act as Regulatory Affairs Submissions support to project teams by guiding submission processes and standards. Participate in and facilitate submission team meetings. Coordinate and manage multiple interrelated submission activities concurrently. Anticipate submission risks and propose solutions to meet timelines. Prepare content planners for publishing and coordinate submission publishing with off‑site vendors. Interface with publishing vendors to resolve publishing issues; may perform limited in‑house publishing tasks. Facilitate the creation or procurement of submission deliverables, including cover letters and regulatory forms. Perform detailed quality reviews of published submissions, including verification of content, bookmarks, hyperlinks, and tables of contents. Ensure compliance with regulatory standards and health authority guidance. Contribute to the development and implementation of internal business processes, standards, and publishing documentation. Suggest and support process improvements, including updates to software and business processes. Demonstrate the ability to influence without direct authority and maintain strong internal and external working relationships. Position Scope Works under supervision with regular oversight from the manager. Responsible for managing assigned projects independently within defined parameters. Provides regular project status updates to the manager. May assist with onboarding and training of new staff. Benefits The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long‑term disability insurance, short‑term disability insurance, paid parking/public transportation, paid time, paid sick and safe time, hours of paid vacation time, weeks of paid parental leave, paid holidays annually (These all are subject to applicable eligibility). Seniority level Entry level Employment type Contract Job function Legal #J-18808-Ljbffr Collabera
- ...Regulatory Affairs Specialist Job Type: Full time - Permanent Location: Madison, New Jersey (On-site) A commercial-stage transplant technology company, part of a global medtech group, is changing how donor organs are preserved and assessed before transplant. Their...SuggestedPermanent employmentFull time
$86.7k - $170.9k
Position Summary Consultant - Regulatory & Compliance - Enterprise Operations & Risk Our Deloitte Regulatory, Risk & Forensic team... ...not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At...SuggestedLocal areaVisa sponsorship$90k - $200k
...a broad range of complex investigations, forensic accounting, regulatory compliance, including business intelligence, internal (client)... ...of Kroll’s expert resources. Oversee and review the quality of Associates, Associate Managers, and Managers research and analysis on the...SuggestedTemporary workFlexible hours$90k - $125k
...R&D facilities and through strategic partnerships with manufactures from around the world. About the Role The Regulatory Affairs Senior Associate is responsible for managing key regulatory submission activities (e.g., ANDAs and post-approval changes), supporting...SuggestedFull timeFlexible hours- Withum is a place where talent thrives - where who you are matters. It’s a place of endless opportunities for growth. A place where entrepreneurial energy plus inclusive teamwork equals exponential results.Explore different industries. Learn new skills. Connect with our...SuggestedFull timeContract workWork at officeLocal area
- ...and provide budgeting/financial flexibility by offering contingent labor as a variable cost.Job Description• Assist and support regulatory CMC managers in the following activities:• Defining global CMC regulatory strategy and decisions for development projects or marketed...Immediate start
- ...independence. This role is designed for a developing risk professional who can execute risk assessments, analyze control evidence, support regulatory and audit requirements, coordinate remediation tracking, and produce clear reporting for stakeholders. The role applies working...
$34.09 - $48.75 per hour
DLA Piper is, at its core, bold, exceptional, collaborative and supportive. Our people are the backbone, heart and soul of our firm. Wherever you are in your professional journey, DLA Piper is a place you can engage in meaningful work and grow your career. Let’s see what...Hourly payWork at officeRemote workRelocationVisa sponsorshipRelocation package- RWJBarnabas Health is seeking a 340B Analyst to support regulatory compliance and 340B program utilization across the hospital system. The role emphasizes audit-driven processes, data integrity, and collaboration with pharmacy leadership to maintain HRSA-aligned operations...
$205.62k - $266.09k
...is office based/hybrid located in Foster City, CA or Parsippany, NJ. As the Sr Director, U.S. Ethics & Compliance Advisor, Medical Affairs, you will report into the Executive Director, U.S. Ethics & Compliance Advisor and you will… Act as the key point of ethics and compliance...Work at officeLocal area$19.5 per hour
Document Processor / Compliance AnalystParsippany-Troy Hills, New Jersey, United StatesDocument Processor / Compliance Analyst (Full-Time - NJ)Business Credentialing Services, Inc. (BCS) is a fast-growing technology company in the insurance and risk management industries...Hourly payFull timeWork at officeRemote workMonday to Friday2 days per week1 day per week$70k - $150k
...Associate Manager, Financial Investigations Kroll's North American Investigations, Diligence and Compliance - Specialist practice... ...a broad range of complex investigations, forensic accounting, regulatory compliance, internal (client) investigations, insider risk compliance...Temporary workInterim roleFlexible hours- ...performance and depending on business needs. Pay Range: $30 to $35/Hour on W2 Shift Timing: 8AM - 4PM EST Essential Functions: Enforce regulatory compliance and quality assurance Prepare and maintain reports of credentialing activities such as accreditation, membership or...Contract workShift work
- ...Credentialing SpecialistEnforce regulatory compliance and quality assurancePrepare and maintain reports of credentialing activities such as accreditation, membership or facility privilegesEnsure that all information meets legal, federal and state guidelines when processing...
$22 - $25 per hour
Credentialing SpecialistAt Ivy Health, we're "All About the People"! As a Credentialing Specialist, you will play a crucial role in our mission to help enable people to live their lives to the fullest.Your responsibilities will include:Maintains current and accurate data...Hourly pay- Company DescriptionLeading Financial Services firm in Florham Park, NJ looking to hire top a Senior Financial Reporting Analyst. Job DescriptionTo adequately review, prepare, and disclose the financial statements for the Bank to members of senior management, SEC as well...
$108k - $143k
...strategies.Familiarity with facilities engineering or critical-facility operations, including the repair and maintenance cost drivers associated with mechanical, electrical, and plumbing (MEP) infrastructure.Experience with NetSuite.Experience organizing operational data or...Permanent employmentFull timeTemporary workCasual workWork at officeFlexible hours$98.99k - $137.13k
DLA Piper is, at its core, bold, exceptional, collaborative and supportive. Our people are the backbone, heart and soul of our firm. Wherever you are in your professional journey, DLA Piper is a place you can engage in meaningful work and grow your career. Let’s see what...Full timeWork at officeRemote workRelocationVisa sponsorshipRelocation package- ...hospital operations, and life sciences in more than 160 countries and regions. Position Summary The position of Senior Regulatory Affairs Specialist is responsible for preparing regulatory submissions (e.g. Q-Submissions, INDs, IDEs and PMAs) for North America...For subcontractorRemote workFlexible hours
- ...at . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description The Senior Associate, Regulatory Affairs Submission Management , manages medium to high impact, moderately complex submission projects involving multiple cross-...Full timeWork at officeLocal areaRemote work
- Job ID: 25659184Reference Number: 25-00595Title: Data AnalystLocation: Whippany, NJPosted Date: 2025-06-06Contact: Rishabh PandeyContact Email: ****@*****.*** Phone: (***) ***-****Company: HAN Staffing Job Decription:We are seeking a highly analytical...
- A leading pharmaceutical firm in New Jersey is seeking a Regulatory Affairs Associate I to manage low- to medium-impact regulatory submission projects. You will be responsible for coordinating submission activities, ensuring compliance with regulatory standards, and working...Contract work
- Withum is seeking a Contract Compliance Senior Consultant for its Risk Advisory practice. The role focuses on royalty audits, franchise compliance audits, revenue participation audits, lease reviews, vendor audits, and related contract-based projects. The Senior Consultant...Contract workWork at office
- The Provider Credentialing & Compliance Coordinator is responsible for managing and maintaining the credentialing, enrollment, licensing, and continuing education requirements for all NJPNI providers. This position serves as the primary administrative resource for provider...
- DLA Piper is seeking a Compliance Coordinator in the United States to support the Office of General Counsel with administrative alignment of compliance operations and due diligence activities. The role sits across multiple offices with a hybrid work schedule. The individual...Work at office
- ...Associate Director leading regulatory strategy for oncology advertising and promotion at AbbVie. Oversees cross-functional teams, manages departmental operations, and develops complex regulatory initiatives with minimal direction. Based in one of four US headquarters locations...
$141.5k - $268.5k
Associate Director, Regulatory Affairs Advertising & Promotion - Oncology Full-time Salary Min: 141500 Salary Max: 268500 Workday Global Grade: 20 Compensation: USD 141,500 - USD 268,500 - yearly About AbbVie AbbVie's mission is to discover and deliver innovative...Full timeWork at officeRemote work$140k - $200k
Overview The Senior Manager/Associate Director, Regulatory Affairs CMC is a strategic and hands on regulatory contributor responsible for defining and executing global CMC regulatory strategies for assigned investigational and/or marketed assets. The role partners closely...Full timeWork at officeLocal area$124.48k - $155.6k
...process optimization, automation, and digital transformation, while ensuring alignment with business goals, enterprise standards, and regulatory requirements.*This role is 2-3 days onsite at our Parsippany, NJ office*The ideal candidate combines strong business analysis...Work at officeLocal areaWorldwideFlexible hours- ...Manage initiatives involving Mark-to-Market (MTM) risk, counterparty credit risk, VaR, collateral eligibility, haircut models, and regulatory compliance (GRC) platforms.Agile Coaching & Transformation: Lead Lean-Agile adoption using SAFe frameworks. Establish Centers of...Contract workOverseas2 days per week
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Regulatory Affairs Associate I. Be the first to apply!
- clinical research regulatory Florham Park, NJ
- regulatory Florham Park, NJ
- regulatory law Florham Park, NJ
- regulatory contract Florham Park, NJ
- legal compliance Florham Park, NJ
- vendor compliance Florham Park, NJ
- regulatory compliance Florham Park, NJ
- pharmaceutical regulatory affairs Florham Park, NJ
- regulatory affairs assistant Florham Park, NJ
- corporate compliance Florham Park, NJ




