Regulatory Affairs Consultant
Socket
Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds…. ClinChoice is searching for an Regulatory Affairs Consultant Hybrid for 3 months Contract to join one of our clients. Job Description: This position is directly responsible for supporting global market access including ensuring products dossiers address regulatory requirements (both existing and emerging). Assemble (gather/create) all necessary technical and registration documentation in conformity with legal regulations of the marketing countries in order to meet local on counter dates. Coordinate and ensure maintenance of Brand/Market Registration Tracking databases in cooperation with affiliate, law firm and distributor counterparts, ensuring consistency and timely registrations and data integrity. Research, generate and distribute registration documentation; including formulas, specifications, Certificates of Free Sale, durability, claims substantiation, supporting declarations and artwork – according to specified local market regulations. Partner with seasoned mentor to provide appropriate support and follow‑up with markets to secure registration and achieve market launch timelines. Maintain and update registration databases in order to ensure end‑to‑end registration compliance and consistency. Provide regular follow‑up with market to ensure accuracy of data and compliance with expiry/re‑registration timelines per market. Interface with trade associations and health authorities to secure brand/product and market specific Certificates of Free Sale. Coordinate additional data and information requests with R&D and Regulatory Compliance, obtaining efficacy reports to support product registration, package claims and durability reports. Liaise with brand GBSC and Marketing to track and obtain final product/shade names and codes. Perform research with brand and/or PDS to obtain all variant/kit/set/size artwork and country of origin information required to action and complete product registration on a sku and/or family level, depending on market requirements. Who will you be working for? About ClinChoice ClinChoice is a global full‑service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high‑quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia‑Pacific. Our Company Ethos Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly‑qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates. ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it. #J-18808-Ljbffr
$119k - $218.3k
Position Summary Senior Consultant - Risk, Regulatory, & Licensing - Digital Assets Regulatory & Financial Risk Ready for a fast-paced, impactful... ...or certification(s) in risk, compliance, regulatory affairs, or a related field (e.g., CRCM, CAMS, CISA, JD, or LLM).Demonstrated...SuggestedWork at office- Overview Regulatory Affairs Consultant - China (IVD / IUO / Software) Location: U.S.-based (remote) Engagement: Contract / Consulting (scope and duration TBD) We are supporting a U.S.-based life sciences company exploring current and future regulatory needs related to...SuggestedContract workRemote work
- This clinical-stage biotech company is revolutionizing the treatment of cancer. They are seeking a Senior Regulatory Affairs Consultant to oversee all regulatory activities and serve as the primary contact with FDA and other regulatory agencies. You will develop and implement...SuggestedFull timeContract workWork at office
- ClinChoice is seeking a Regulatory Affairs Consultant on a hybrid, 3-month contract to support global market access and regulatory submissions. The role involves assembling technical dossiers and maintaining registration data across markets. You will coordinate with R&D...SuggestedContract work
- Parexel International is seeking a Regulatory Affairs Consultant (Regulatory Intelligence) to join a strategic partnership, tasked with monitoring and analyzing regulatory developments. This role can be home-based or office-based and requires a university degree in a scientific...SuggestedRemote jobWork at officeWork from home
- Job Title: Regulatory Affairs SpecialistREMOTEContract: 1 Year and Possibility of ExtensionClient is seeking an experienced Regulatory Affairs contractor to support the preparation and submission of a US FDA 510k and the development of global regulatory documentation,...For contractors
$72k - $141k
...fullest potential. The Compliance Senior Consultant is a strategic individual contributor... ...advancing key compliance programs, enhancing regulatory responsiveness, and facilitating... ...experience in insurance, compliance, regulatory affairs, or audit.Demonstrated ability to...Full timeWork experience placementWork at office- ...Job Overview: We are seeking a detail-oriented Regulatory Associate to join our Regulatory Affairs team. In this role, you will play a vital part in supporting the development and submission of regulatory documents, ensuring compliance with all regulatory standards,...Contract workWork at office
- ...ICapital is looking for a Compliance Associate to join its Regulatory and Compliance team to lead the review and approval process for marketing materials created by our investment advisers and broker‑dealer There will be a strong focus on marketing materials for private...
- ...a crucial bridge between local commercial teams and regional regulatory bodies to guarantee patient access to life-saving medical devicesThis... ...preferredMinimum 4 years of relevant experience in regulatory affairs within the medical device or healthcare industryWorking...Local area
$80k - $105k
Who we are For over 25 years, Global Relay has set the standard in enterprise information archiving with industry‑leading cloud archiving, surveillance, eDiscovery, and analytics solutions. We securely capture and preserve the communications data of the world’s most highly...Temporary workWork experience placementWork at office$30 - $34 per hour
*W2 ONLY* The Fountain Group is currently seeking a Regulatory Affairs Analyst for a prominent client of ours. This position is Remote . Details for the position are as follows: Job Title: Regulatory Affairs Analyst Location: Remote Pay Rate: $30-34/Hour Duration: 6 Months...Local areaRemote work- ...Overview We are looking for an experienced banking regulatory compliance professional to support multiple community bank, credit union and fintech clients on a project basis. This contract role is fully remote and 15-20 hours per week with a duration of 4 months. Responsibilities...Hourly payContract workLocal areaRemote workFlexible hoursShift work
- ...message the job poster from Medasource Regulatory Compliance Specialist – EU Clinical... ...regulatory compliance—not just regulatory affairs—and be ready to make an immediate impact... ...type ~ Full-time Job function ~ Consulting Industries ~ Pharmaceutical Manufacturing...Full timeContract workImmediate startRemote work
- ...Protective Life Insurance Company is seeking a Senior Compliance Analyst for Regulatory Affairs and Market Conduct. You will work with regulators to manage inquiries and examinations, researching rules and drafting responsive positions with internal partners. The role...
- ...Planet Pharma is seeking a Site Activation professional to support feasibility, site identification, regulatory start-up and maintenance activities in accordance with SOPs and project requirements at regional or country level. You will prepare and review site documents...
- ...Bachelor's Degree or equivalent in scientific discipline (e.g., Biology, Microbiology, Chemistry) 7+ years of experience Regulatory Affairs required Support US and EU regulatory submissions (exercising judgment to protect proprietary information); track timelines and...Work at office
- ...International EMEA Ops team to scale operations for Coinbase Ireland Limited across the EEA. You'll drive day-to-day operations, regulatory reporting, outsourcing oversight, and cross-functional initiatives to support growth and compliance. The role requires 5+ years in...
- ...competitive benefits include medical and dental coverage, a matching 401(k), and paid time off to recharge. Job Description: The Regulatory Affairs Assistant supports efforts to ensure regulatory submission targets are met. Completes all duties under the direction of the...Work at office
- ...Regulatory Affairs Specialist (Cosmetics) A growing beauty and personal care company is seeking a Regulatory Affairs Specialist to support global regulatory compliance, product safety activities, and day‑to‑day regulatory operations across domestic and international markets...Work at office
- ...documents remain current. Assist with drafting policy language and formatting documents. Collaborate with stakeholders to monitor regulatory changes and support policy alignment. Prepare and maintain reports and documentation related to policy management and compliance....
- ...BCG Attorney Search seeks a skilled Trade Remedies Associate for its Government and Regulatory Affairs practice in New York City, NY. The successful candidate will handle complex investigations and litigate cases before the U.S. Court of International Trade, possessing...
- ...Due to continued growth and the ongoing success of our Regulatory Affairs Consulting team, Parexel is seeking an experienced Senior Regulatory Affairs Consultant (Program / Client Partnership Manager) to join our team. In this pivotal role, you will leverage advanced...
$219k - $273.8k
...Mercury Invest* are in some ways still taking shape and must continually rise to the occasion to meet evolving customer needs. The regulatory frameworks are complex, the product roadmap is ambitious, and the person in this role will have a direct hand in the high quality...Work from homeFlexible hoursShift work$87.58k - $120.42k
...challenges us to be better every day, driven by our agile, performance-focused culture. About the Role This Senior Associate, Regulatory Affairs role is responsible for independent execution of regulatory activities for defined products, workstreams, or deliverables...Work at office- ...service of our vision to empower people to continue forward with their lives – cancer free. The role: The Senior Associate, Regulatory Affairs will be a key individual contributor on a small, high-impact regulatory team and will report directly to the Vice President,...Flexible hours
$55.03 per hour
...learn more. Base pay range $55.03/hr - $55.03/hr Direct message the job poster from Infosoft, Inc. Job Title: Senior Regulatory Affairs Specialist Pay Rate: $50 to $55.03/HR Duration: 6 months Location: Irvine, CA/Remote (9 am to 6 pm PST time zone...Full timeWork at officeRemote work- ...A global management consulting firm based in New York is seeking a talented Management Consultant to support its Risk, Regulatory & Compliance Business Unit. Responsibilities include leading client delivery initiatives and managing projects in a complex regulatory environment...
- A biopharmaceutical company is seeking a Senior Manager, Global Regulatory Affairs Labeling to lead its global labeling initiatives. This role involves strategy development for labeling, ensuring compliance, and managing cross-functional stakeholder reviews. Candidates...Remote work
- ...Supply Chain) to collect and verify documentation related to pre or post-approval stages. Represent Syneos in cross-functional regulatory and Client teams meetings. Act as a subject matter expert and help the team members with day-to-day trouble shooting...
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