Regulatory Affairs Specialist-V
Artech Information Systems LLC
Company DescriptionArtech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.Job DescriptionThis 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. Skills: 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. . QualificationsBachelor 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 experienceAdditional Information Sneha ShrivastavaTechnical Recruiter (Clinical/Scientific)Artech Information Systems LLC360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: View phone number on click.appcast.io | Fax: 973.998.2599Connect with us on - LinkedIn | Facebook | TwitterSummaryType: ContractFunction: ResearchExperience level: ExecutiveIndustry: Pharmaceuticals
- ...both internal and external cross-functional project teams.• The Regulatory CMC Technical Associate may be called upon to author technical... ...Master s Degree a plus• 4+ years of pharmaceutical regulatory affairs experience• Strong knowledge of NDA, ANDA, MAA, BLA, CTA, or...SuggestedWork at officeLocal areaImmediate start
- ...Regulatory Affairs Specialist III Location: Bridgewater, NJ Duration: 9 Months Manager will consider candidates to be based in either Bridgewater, New Jersey or Cambridge, Massachusetts. Please specify on resume which location candidate is being submitted for....SuggestedWorldwide
- ...accountability and commitment.Strong knowledge of international good clinical practices (ICH) and thorough understanding of current regulatory requirements (FDA, EMEA) related/ applicable to the conduct of clinical trials, understanding of FDA Compliance Manual & EMA...SuggestedImmediate startRemote work2 days per week
- ...the strategic priorities that impact the near term and long term priorities of Client's development program.s Alignment with Medical Affairs for global strategic study placement decisions is also expected for phase 3 programs. To better serve some customers experience or...SuggestedLocal areaImmediate startFlexible hours
$148k - $170k
...environment that promotes professional growth and a significant impact on patients' lives.Reporting StructureReports To: Director, Regulatory Affairs - Advertising, Promotion, and LabelingDirect Report(s): NoneAreas Managed: Advertising & Promotion North AmericaOverviewThis...SuggestedNight shiftWeekend work- ...Regulatory Affairs Associate As a Regulatory Affairs Associate you will: Gain experience and exposure to groundbreaking programs and strategies for compounds in development and/or marketing products intended to address unmet medical needs in markets globally. Learn...
- Company DescriptionAt the forefront of the staffing industry, Artech is a women-owned business enterprise (WBE) committed to maximizing global workforce solutions on behalf of its clients. Artech's deep heritage, proven expertise and insightful market intelligence has secured...Work at officeLocal area
- Urgent Need – Data Analyst (Strong Medallion Architecture) – Raritan, NJ – Hybrid (C2H - Only W2) Hi, We are hiring candidates for following requirement, kindly send let me know if you are interested and share me your resume. Data Analyst (Medallion Architecture...Long term contract
- Why Messer? Messer is the world’s largest privately held industrial gases company and what we do matters because it is woven into every part of life, from the medical gases that patients rely on to the essential elements needed to safely and sustainably produce the goods...Permanent employmentFull timeTemporary work
$90k - $118k
...assessment, reconciliation, governance, and business analytics initiatives that drive operational excellence, transparency, and regulatory compliance.Key ResponsibilitiesWork closely with business and functional analysts to develop functional and technical requirements...Full timeTemporary workWork at officeLocal areaRelocation package3 days per week$94.5k - $165k
...and play by connecting them to what brings them joy. We do what we love — driving innovation, creativity, and impact in the world. Our V Team is a community of people who anticipate, lead, and believe that listening is where learning begins. In crisis and in celebration,...Full timeTemporary workPart timeWork experience placementWork at officeWork from homeShift work3 days per week- Clinical Data AnalystA Few Words About Us 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 1...
- ...performance, this is an exciting opportunity to support the growth of the captive reinsurance business, become an expert in the Bermuda regulatory framework, and gain exposure across a variety of risks and markets.Location: This role will be based in Hamilton, Bermuda....Full timeWork at officeRelocation package3 days per week
$86.58k - $123.3k
...and consumers. POSITION OVERVIEW: The Senior Regulatory Operations Specialist is an experienced individual contributor who plans,... ...global regulatory submissions. The role works with Regulatory Affairs, content owners, technology teams, and external providers...Remote work- Responsibilities: Excellent employment opportunity for a Clinical Data Analyst in the Raritan, NJ area. The Data Entry Analyst is needed to support re-creation of clinical trial data into Medidata CTMS system. Knowledge of the Clinical Trial Management...Monday to Friday
$116.3k - $155.1k
General Information LocationNew York, New York Alternative Location(s) Posting Location:Bridgewater, New JerseyPosting Location:St Louis, Missouri Working Schedule Full-Time Work Arrangement Hybrid Relocation Assistance Available No Grade 12C ...Full timeTemporary workWork at officeLocal areaRelocation package3 days per week- Clinical Data Analyst III Contract Company Description IRI believes in commitment, integrity and strategic workforce solutions. Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions...Contract work
$154.38k - $193.13k
Job DescriptionPrincipal - Business Consulting (SAP Program Manager)About UsDo you want to boost your career and collaborate with expert, talented colleagues to solve and deliver against our clients' most important challenges? We are growing and are looking for people to...Full timeTemporary workLocal areaRemote work$110k - $146k
Why Messer? Messer is the world’s largest privately held industrial gases company and what we do matters because it is woven into every part of life, from the medical gases that patients rely on to the essential elements needed to safely and sustainably produce the goods...Full timeTemporary workFor contractors$135k - $180k
...tracking schedule to complete on time.• Provide a quality project while minimizing unbudgeted change orders.• Manage interface with regulatory agencies to ensure compliance with adopted environmental, life safety and technical code references.• Organize required internal...Full timeContract workTemporary workFor contractors$165k - $218k
Description and Requirements The Team You Will Join Join our Global Risk Management Group, where you’ll play a key role in safeguarding the company, ensuring we deliver on our commitments to customers and stakeholders, and driving responsible growth. As part of our...Temporary workWork at officeLocal areaShift work3 days per week- About the job Pricing Data Analyst We are looking for a highly motivated, detail-oriented Pricing Data Analyst to support our global product portfolio activities across their full lifecycle. In this role, you will act as a key contributor to portfolio transparency...Work at office
- Data Analyst IIParticipation in the data analytics activities for the Winthrop and Legacy Brand U.S. portfolio.Duties include:Compilation and analysis of raw data for customer returnsCompilation and analysis of raw data for customer deductions on invoiceCompilation and ...
- ...Job Title: Regulatory Specialist Ready to apply Before you do, make sure to read all the details pertaining to this job in the description below. Work Location: Middlesex County, New Jersey Summary: The Regulatory Specialist is responsible for supporting regulatory...
- ...employees. Including lab draws and vaccinations. Ensures delivery of integrated services in accordance with Health & Wellness and regulatory guidelines and in alignment with the business needs of our customers. Conduct medical surveillance procedures as directed to...
$28.5 - $35 per hour
...compliance with state and federal regulations. Responsibilities include oversight of sample collection, development and review of regulatory reports, and assistance in the implementation of new environmental compliance initiatives. The ideal candidate should have...Hourly payTemporary workWork at officeLocal areaMonday to Friday- ...Phase I/II clinical studies ~ Experience in cell therapies, gene therapy, biologics, or vaccine development ~ Familiarity with regulatory requirements (FDA regulations and/or GxP guidelines), ~ CMC requirements, and clinical study execution ~ At least 5 years of...Full time
$86.9k - $121.88k
...this job. Duties, responsibilities, and activities may change at any time with or without notice.The Senior Healthcare Compliance Specialist supports the development, implementation, and continuous improvement of the Terumo Corporate Compliance Program at Terumo...Contract workTemporary workLocal areaImmediate startWorldwideFlexible hours$46k - $111k
Choosing Capgemini means choosing a company where you will be empowered to shape your career in the way you’d like, where you’ll be supported and inspired by a collaborative community of colleagues around the world, and where you’ll be able to reimagine what’s possible...Full timeLocal area$143.1k - $238.5k
...Lead community events and expand involvement in community affairs and other centers of influence to promote the bank's image.... ...documentation and technical exceptions. Stay compliant with all regulatory and bank risk compliance matters. Provides mentoring and guidance...Full timeTemporary workWork experience placementWork visaFlexible hours
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