Regulatory Affairs Specialist V-41593
Makro Scientific
Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific’s proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing innovation and decreasing costs while maintaining the complex service level expectations. Our global presence with offices in USA (NJ, PA, IL, CA) and offices in UK, Europe and Asia enables us to be a powerful contributor and connector of right Talent. Job Description This individual will be part of the Global Regulatory Affairs team and assists with planning, writing, compilation, and editing of periodic regulatory reports (i.e. DSURs, orphan annual updates, NDA annual reports, PBRERs). With oversight and guidance, contributes to the generation of product regulatory strategy documents (for products in phase 1-3 clinical development), labeling updates for marketed products, generation of FDA meeting requests and corresponding briefing materials, and other tasks as needed. Qualifications Working knowledge of FDA and ICH requirements for standard regulatory documents and their maintenance. Excellent written and verbal communication skills, with ability to organize and manage multiple priorities. Proficiency in MS Word, Excel, and PowerPoint. Self‑starter with the ability to work independently but seeking out guidance as needed. Technical aptitude to work across multiple information systems and databases with ability to troubleshoot. Sense of urgency and perseverance to achieve results. Education Bachelor’s degree and at least 5 years in Regulatory Affairs or relevant industry experience, or Master’s, PharmD, PhD degree and 3 years in Regulatory Affairs or relevant industry experience. Additional Information Need someone that has worked on a regulatory team, preparing regulatory documents. Candidates will need to understand the content; really looking at regulatory strategy and drug development and synthesizing that information for reports. #J-18808-Ljbffr Makro Scientific
- ...execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.Job Description• The Regulatory Affairs Operations (RA Ops) submission group is organized to provide submission development support to project teams and the...SuggestedImmediate start
$120k - $160k
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$147.4k
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$80k - $150k
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...Biogen's US business. Your expertise will ensure that our business operations adhere to the highest standards of compliance and regulatory conduct. By developing and delivering comprehensive training programs, you'll be an educational pillar for both new and established...Full timeTemporary workWork at officeLocal area- ...must have at least (A) four years of full-time, or equivalent part-time, experience in investigatory or law enforcement work, or regulatory administration work (B) and equivalent combination of the required experience and the substitutions below.Substitutions:A Bachelor...Full timeContract workTemporary workPart timeWork experience placementWork at officeRemote work1 day per week
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$150k - $200k
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...Health And Welfare Benefits Compliance Specialist TELUS Health is empowering every person to live their healthiest life. Guided by... ...to join our U.S. Benefits Administration Compliance team. The Regulatory Compliance Specialist plays a critical role in ensuring that TELUS...Work at officeFlexible hours- ...Regulatory Affairs Associate Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our...
$90k - $200k
...management and enhancement of client relationships.Plan and manage a broad range of complex investigations, forensic accounting, regulatory compliance, including business intelligence, internal (client) investigations, insider risk compliance assessments, consulting projects...Temporary work$260k - $360k
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- ...risk programs including the review of marketing and advertising materials in compliance with the Advisers Act and other relevant regulatory requirements, compliance specific client reporting, and code of ethics review and enforcement. Preparation and filing of required...
$70k - $90k
...Compliance Specialist CopperPoint has an exciting opportunity for a Compliance Specialist. In this role, you'll help develop and administer an effective regulatory compliance program that ensures adherence to state regulatory and statutory requirements. You'll research...Hourly payTemporary workFlexible hours- ...Compliance Specialist Boston, MA Responsible for providing the independent monitoring of investment compliance requirements so as... ...firm's ongoing compliance; advise key business units in related regulatory and client compliance requirements; train investment...Work experience placement
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