Compliance Specialist
Tower Legal Solutions
Legal Administrative Consultant job at Tower Legal Solutions. Bedminster, NJ. Our client, a large telecommunications company is seeking temporary legal administrative staff (see shifts below) to work onsite in its Bedminster, NJ offices assisting its Court Order Compliance Group. Job function includes data entry of legal process into client's workflow management system and answering time-sensitive incoming calls. Please note this is a high-volume environment requiring strict confidentiality and attention to detail. Confidentiality and attention to detail are a must. The position is a long-term temp role expected to start immediately. A four-year college degree is required. Any legal background, education or legal experience is preferred. Key Responsibilities : Communicate with the law enforcement community in connection with customer and account data. Authenticating caller information in coordination with law enforcement personnel. Ensure all cases are correctly documented and managed end-to-end in compliance with company procedures. Entering customer and account data from source documents in a timely manner and reporting needed changes. Strong customer service or dispatch-like experience for handling high call volumes of a dynamic nature. Compiling, verifying the accuracy and sorting information to prepare source data for computer entry. Reviewing data for deficiencies or errors, correcting any incompatibilities and checking output. Resolves deficiencies by using standard procedures or returning incomplete documents to the team lead/supervisor for resolution. Requirements : The ability to work independently. Accuracy and Attention to detail. Understanding of and willingness to learn about basic legal concepts. Customer Service experience a plus. Proficient in typing and transcription. Computer and technical skills. Organizational and time management abilities. Administrative skills, copying, filing, sorting and mail distribution. Strong Communication Skills (written and verbal). Candidate must be eligible to apply for a government clearance. Shifts: Sun-Thurs 6PM-3AM; Tues-Sat 3PM-12AM. #J-18808-Ljbffr
- 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. ...Suggested
- Join to apply for the Data Consultant role at SDG Group USA Join to apply for the Data Consultant role at SDG Group USA This range is provided by SDG Group USA. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay...SuggestedFull timeInternshipLocal areaRemote workFlexible hours
- ...products and an entrepreneurial mindset. Role Description: dThe Regulatory Affairs (RA) Specialist is responsible for supporting global regulatory submissions and compliance activities to ensure medical device products meet applicable regulatory requirements...SuggestedInternshipWork at officeWorldwide
- ...professional development. Summary of the Role We are looking for an experienced and dynamic Permitting & Regulatory Compliance Specialist II to join our growing team. In this role you will independently manage a defined caseload of permitting and compliance...SuggestedWork at officeImmediate startRemote workFlexible hours
$166.72k - $250.08k
...regulatory review, guidance, risk assessment, and mitigation recommendations for branded and unbranded promotional materials to ensure compliance with FDA advertising and promotion requirements, approved labeling, internal policies, and company standards. Review a broad...SuggestedWork at office$18 - $20 per hour
...Credentialing and Provider Enrollment Specialist Job Category : Human Resources Requisition Number : CREDE003404 Posted : August 3, 20... ...and documentation. Assist with provider updates, renewals, and compliance requirements. Provide general administrative support as needed...Full timeShift work- Strong compensation & benefits package. Opportunities for growth and development. About Our Client Our client is a well-established site development and utility contractor serving New Jersey's public and private sectors. The company specializes in earthwork...Contract workFor contractorsFor subcontractorLocal area
$71.25k - $116k
...drives business value while ensuring alignment with GxP requirements, data integrity principles and regulatory expectations. The IT Compliance analyst helps enable business effectiveness by identifying opportunities across business areas for leveraging technology, process...Temporary workWork experience placementRelocation packageFlexible hoursShift work$90k - $125k
...package preparation. Responsibilities Compile and submit ANDAs, supplements (CBE/PAS), annual reports, and labeling supplements in compliance with FDA requirements. Author relevant eCTD sections using company templates and ensure files are properly formatted with...Flexible hours- ...vendor contracts and renewals; monitor service quality, timelines, and SLAs; escalate and resolve service issues. -Ensure vendor compliance with company requirements (e.g., insurance, access procedures, safety expectations) as applicable. Expat Support -...Contract workWork at officeLocal areaRelocation
- ...for OTC products, review claims and copy. • Participate in the review of promotional materials. • Support end-to-end regulatory compliance of products in remit. • Apply system and procedure updates to maintain up-to-date technical product records. • Identify and...Hourly payContract workLocal area
$86.58k - $123.3k
...POSITION OVERVIEW: The Senior Regulatory Operations Specialist is an experienced individual contributor who plans, coordinates... ...recommend solutions, and escalate issues that may affect quality, compliance, cost, or timing. Represent Regulatory Operations on submission...Remote work- ...Senior Associate, Regulatory Operations to lead US regulatory submissions to the FDA, maintain eCTD templates, and ensure FDA/ICH compliance. You will also manage document workflows and corporate records, enabling timely submissions. The role requires strong...
- Our client is currently seeking a Data Analyst II The CX Insights and Engagement Team designs and implements a best-in-class Voice of the Customer (VOC) program to drive customer-centric decision-making. This role requires strong communication, interpersonal...Work experience placement
- Clinical Data Analyst A 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 ...
- 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
$88.2k - $125.5k
...individuals with disabilities. If you need an accommodation to apply for a job in the U.S., please email the CGI U.S. Employment Compliance mailbox at ****@*****.*** . You will need to reference the Position ID of the position in which you are interested...Work at officeLocal areaRemote work2 days per week3 days per week- Clinical Data Analyst III Client: Direct Client Location: Raritan, NJ Job Title: Clinical Data Analyst III/Clinical Data Manager III Position Duration: 1 year+ Job responsibilities: • Clinical Data Analyst is responsible for CTMS and Grants Manager study...
- ...Data Management: Monitor inbound/outbound data feeds with third-party vendors and ensure high data quality, security, and privacy compliance # Testing & Quality Assurance: Design test scenarios, coordinate UAT, and troubleshoot system defects before launching updates...
- 1 year contract with high probability of extensions hybrid in Spring House, PA OR Raritan, NJ (2-3 times onsite per week) ASAP start Position Overview We are seeking an experienced Regulatory Program Manager to support global oncology programs within a large pharmaceutical...Contract workWork at officeImmediate startWorldwide
$77k
Compensation $77,000.00 - $77,000.00 / Yearly Hours Per Week 40 Number Of Positions 1 Job Description Title: Actuarial Analyst Company: Everest Global Services, Inc. Job Category: Analytics Job Description: About Everest: Everest...Full timeWork at officeHome office$100k - $150k
Senior Actuarial Analyst Everest is a global leader in risk management, rooted in a rich, 50+ year heritage of enabling businesses to survive and thrive, and economies to function and flourish. We are underwriters of risk, growth, progress and opportunity. We are a ...Full time- CMG Networks seeks an experienced accounting professional in Bedminster, NJ to manage government contracts. Responsibilities include AR/AP, invoicing, and close processes. Requires 3+ years public accounting and 5+ years FAR-based government contracting experience, with...
- Paradigm Infotech. Inc is a global IT solutions provider focused on delivering customer value through high quality processes and cost-efficient solutions. Paradigm has been one of the trendsetters in global delivery practices with our client‑centric model for customer ...
$184k - $230k
...more than 300 dedicated employees across all functional areas. Innovating every day. Position Summary The Director, Compliance leads the day-to-day design, implementation, and continuous improvement of Cosette Pharmaceuticals' enterprise compliance program...Contract workTemporary workFor contractorsFixed term contractWork at officeFlexible hours3 days per week- Johnson & Johnson Innovative Medicine R&D is seeking a Senior Manager, North America Regulatory Liaison. This hybrid role will be located in Spring House, PA; Titusville, NJ; or Raritan, NJ. You will lead NA regulatory strategy and execution for Immunology projects, partnering...
- ...commissioning to achieve project goals. The role emphasizes proposal development, PDES strategy, vendor management, and regulatory compliance. A Bachelor's degree in a relevant field and 15 years’ experience in industrial gas or chemical processing are expected. #J-18808...
- ...product under a global alliance. The role oversees CCDS, US/EU labeling, and country-specific labeling reviews to ensure regulatory compliance and timely delivery across regions. The position leads Global Labeling Strategists, collaborates with Regulatory Affairs,...
$139.51k
Job Description Job Description 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...Permanent employmentTemporary work- 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...Work at officeImmediate start
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