Healthcare Regulatory Associate
$200k - $320kJobot
Job details: A nationally recognized healthcare and life sciences law firm is seeking an experienced Healthcare Regulatory Associate in New Jersey or New York to join its growing practice. Salary: $200,000 - $320,000 per year A bit about us: Healthcare Regulatory Associate New Jersey / New York A nationally recognized healthcare and life sciences law firm is seeking an experienced Healthcare Regulatory Associate to join its growing practice. This is an excellent opportunity for an attorney who wants to build a sophisticated, highly specialized practice advising healthcare providers, organizations, investors, and businesses on complex regulatory, transactional, reimbursement, compliance, and enforcement matters. The successful candidate will work closely with experienced healthcare attorneys and have meaningful client contact, substantive responsibility, and exposure to matters involving federal and state healthcare regulations, business structuring, fraud and abuse, licensing, reimbursement, and government investigations. Why join us: Why Consider This Opportunity? This role offers the opportunity to join a law firm whose platform is specifically built around healthcare and life sciences rather than treating healthcare as a small component of a broader general practice. Compensation A highly concentrated healthcare regulatory practice. Substantive work involving healthcare business models, compliance, reimbursement, and transactions. Direct access to experienced healthcare attorneys. Significant client contact and opportunities to develop trusted advisory relationships. Exposure to a broad range of healthcare providers and emerging healthcare businesses. The ability to develop deep expertise in fraud and abuse, licensing, reimbursement, privacy, and transactional healthcare matters. Meaningful drafting and counseling responsibility. Strong opportunities for professional development and long‑term advancement. A collaborative, entrepreneurial environment that values initiative and subject‑matter expertise. The anticipated base salary range is approximately $200,000–$325,000, depending on experience, qualifications, practice depth, market considerations, and the overall strength of the candidate’s background. Additional compensation and benefits may also be available. Job Details Key Responsibilities Advise healthcare providers and businesses on federal and state regulatory requirements. Counsel clients regarding the Anti‑Kickback Statute, Stark Law, False Claims Act, fee‑splitting restrictions, and corporate practice of medicine requirements. Analyze proposed healthcare business arrangements and recommend compliant structures. Draft and negotiate physician employment agreements, professional services agreements, management services agreements, medical director agreements, vendor agreements, and other healthcare contracts. Advise physician groups, medical practices, pharmacies, laboratories, ambulatory surgery centers, behavioral health organizations, telehealth companies, and other healthcare entities. Counsel clients on provider enrollment, credentialing, reimbursement, billing compliance, overpayments, audits, recoupments, and payor disputes. Assist with healthcare transactions, including regulatory due diligence, change‑of‑ownership matters, licensing, entity structuring, and post‑closing integration. Advise on HIPAA, HITECH, business associate agreements, privacy, data use, and information‑sharing requirements. Develop and assess compliance programs, policies, procedures, and training materials. Conduct internal compliance reviews and investigations. Advise clients regarding voluntary disclosures, self‑disclosures, and responses to government inquiries. Prepare legal memoranda, regulatory analyses, client alerts, policies, agreements, and other client‑facing work product. Monitor developments in federal and state healthcare laws and provide practical guidance to clients. Work collaboratively with attorneys across healthcare litigation, corporate, employment, pharmacy, reimbursement, and life sciences practices. Qualifications Meaningful healthcare regulatory experience gained at a law firm, government agency, healthcare organization, or comparable legal environment. Experience with several of the following: Anti‑Kickback Statute Stark Law False Claims Act Corporate practice of medicine Fee‑splitting restrictions Medicare and Medicaid Healthcare licensing Provider enrollment Reimbursement and payor matters HIPAA and healthcare privacy Healthcare transactions Strong legal research, writing, drafting, analytical, and communication skills. Ability to understand complex healthcare business arrangements and provide practical, business‑oriented advice. Strong client‑service skills and comfort communicating directly with healthcare executives, providers, compliance personnel, and business owners. Ability to manage multiple matters and competing deadlines. Excellent judgment, attention to detail, and organizational skills. New Jersey Bar admission is required or must be obtainable promptly. New York admission is helpful. Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, age (40 and over), disability, military status, genetic information or any other basis protected by applicable federal, state, or local laws. Jobot also prohibits harassment of applicants or employees based on any of these protected categories. It is Jobot’s policy to comply with all applicable federal, state and local laws respecting consideration of unemployment status in making hiring decisions. Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance. Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from Jobot, and/or its agents and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. 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$200k - $320k
...Healthcare Regulatory Associate Pine Brook,NJ, US Job Details Experience: Mid Level Salary: $200,000 - $320,000 per year Key Responsibilities Advise healthcare providers and businesses on federal and state regulatory requirements. Counsel clients regarding the Anti-Kickback...Suggested- Jobot is seeking an experienced Healthcare Regulatory Associate in New Jersey or New York to join a nationally recognized healthcare and life sciences law firm’s growing practice. The role involves advising on federal and state healthcare regulations, contracts, licensing...Suggested
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$19.5 per hour
...week. ~ Semi-Annual Pay Increases - Employee can earn up to a 2.5% pay rate increase every six months based on performance. ~ Healthcare Benefits (Medical, Vision, Dental) are available for employees on their first day of employment. ~401(k) / Retirement Benefits...Hourly payFull timeWork at officeRemote workMonday to Friday2 days per week1 day per week- ...automotive compliance experience highly preferred. Duties/Responsibilities Identify business functions and practices that require regulatory activities and assist the compliance management team in developing a compliance strategy. Maintain a proactive approach to...
- ...Job Description Job Description Description: The Regulatory Affairs Sr. Associate is an experienced medical device regulatory professional who can independently support and, where appropriate, lead regulatory activities across the product lifecycle. This role is...Work at office
- ...accompanying documentation, to ensure files meet regulatory requirements. 20% Documents and... .... Responds to inquiries from other healthcare organizations and interfaces with... ...Qualifications Education ~ Associates' degree in Business or Healthcare Administration...Hourly payFull timeTemporary workPart timeFor contractorsFor subcontractorWork at officeFlexible hoursShift work
$122.85k - $163.81k
About the Role:We have a current opening for a Governance, Risk & Compliance (GRC) Specialist, North America and are actively reviewing applications.As the Governance, Risk & Compliance (GRC) Specialist, North America, you will play a key role in strengthening enterprise...Work experience placement- Bankers Life is seeking Financial Advisors who help clients live more and worry less through personalized financial planning. You will build a client base, present financial solutions, and take ownership of your business with the support of industry-leading training and...
- Balazs in Fairfield, NJ, is seeking a Regulatory Specialist to drive compliance excellence for their Cosmetics and Nutrition divisions. This role is vital in managing global documentation requests and adhering to FDA guidelines. The ideal candidate will have a strong foundation...
- Englewood Lab, Inc. is seeking a Regulatory Affairs Associate in Totowa, NJ (onsite) to support the Manager of Regulatory Affairs with inspections, audits, and regulatory submissions. You will help create and maintain Product Master Files, Drug Master Files, and various...
- Seppic Inc., located in Fairfield, NJ, is looking for a Regulatory Specialist to join its team. This role is pivotal in managing compliance and documentation for the Cosmetics and Nutrition divisions. You will serve as the primary contact for customer inquiries and ensure...
- VitalAire Canada Inc. is seeking a proactive Regulatory Specialist based in Fairfield, NJ. This role involves ensuring compliance excellence and managing global documentation requests while collaborating closely with stakeholders. The position offers a salary range of...
- ...years of compliance experience, preferably in automotive F&I. Responsibilities include supporting compliance programs, maintaining regulatory functions, and drafting contracts. The company offers competitive compensation, benefits, corporate events, and a collaborative...
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$20 per hour
Parsippany-Troy Hills, New Jersey, United States Document Processor Contractor (Full-Time - NJ) Business Credentialing Services, Inc. (BCS) is a fast-growing technology company in the insurance and risk management industries. We are growing our Operations department and...Hourly payFull timeFor contractorsWork at officeRemote workMonday to FridayFlexible hours- 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
- Job Description Growing Environmental Consulting firm looking for a Regulatory Compliance Specialist with 10+ Years of Experience. Seeking a professional with project experience to ensure environmental permitting, periodic reporting, training, and other compliance obligations...For subcontractor
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- ...verifications and accompanying documentation, to ensure files meet regulatory requirements. 20% Documents and tracks performance... ...Continuous Query Renewals. Responds to inquiries from other healthcare organizations and interfaces with internal and external customers...Full time
$58k - $70k
Regulatory Affairs Associate Location: Totowa, New Jersey (Onsite) Employment Type: Full-Time / Exempt Department: Quality / Regulatory Reports To: Manager of Regulatory Affairs Position Summary The Regulatory Affairs Associate will assist the Manager of Regulatory...Full timeWork at officeLocal areaMonday to Friday- ...coordinate inspections with officials and company representatives. The role requires strong communication skills, experience with CRM systems, and the ability to read plans and understand regulatory requirements related to real estate. #J-18808-Ljbffr Tuff Shed, Inc.Local area
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