Job Market Guide: Regulatory Affairs Associate jobs - Nationwide

Competition
Avg
0.352256
Based on job seekers per open jobs
Desired Skills
Years of Experience
Years of Experience distribution graph for Regulatory Affairs Associates in Nationwide. Regulatory Affairs Associates in Nationwide have between ${} and ${} years of experience, averaging $${} years of experience.

15 Regulatory Affairs Associate jobs - Nationwide

Scottsdale, AZ
Work closely with the area Director and matrixed business partners communicating the status of regulatory communications and escalate concerns for deadlines and content quality as well as identifying and addressing system restraints on delivery of regulatory .
industry
Biotech/Pharma
experience
8 - 10 years

Princeton, NJ
Designs and develops programs, processes and systems used to ensure accuracy and completeness of regulatory submissions, filings and tracking methods. Develops and analyzes alternative solutions.
industry
Business Services
experience
8 - 10 years

Parsippany, NJ
The Senior Regulatory Associate will with minimal guidance, prepare, review, and submit high quality, regulatory submissions to the FDA within company timelines and in accordance with regulatory guidelines and applicable federal laws. Submissions include amendments, supplements, and annual reports in accordance to FDA guidelines.
industry
Biotech/Pharma
experience
5 - 7 years

Rockville, MD
Provide regulatory guidance in cross-functional teams; performing regulatory review of trial related documents, processing of serious adverse event reports.
industry
Advertising & Marketing Services
experience
5 - 7 years

MIRAMAR, FL
Evaluates issues / problems, proposes solutions and implements action plans / process improvements, informing and escalating as appropriate. Works with other functional areas to resolve issues related to regulatory submissions, compliance, and internal processes.
industry
Biotech/Pharma
experience
5 - 7 years

Billerica, MA
The Regulatory Affairs Recruiting Lead will help all North American EMD legal entities remain compliant with government regulations and restrictions.
industry
Business Services
experience
5 - 7 years

$50K - Raritan, NJ
Provides operational and project support to the Regulatory Information Management team in Global Regulatory Affairs by entering and reviewing data in our Registration and Planning and Tracking applications, providing administrative support for review and approval of compliance related documents, and creating reports.
industry
Biotech/Pharma
experience
Not Specified

Tucson, AZ
Acts as the Regulatory liaison with FDA and international registrars on behalf of the organization to facilitate timely and favorable review of submissions and issues.
industry
Healthcare IT
experience
5 - 7 years

Somerville, NJ
Work with the Regulatory Affairs Business Product Owners to translate business needs for IT solutions and develop/document user stories and/or requirements.
industry
Biotech/Pharma
experience
5 - 7 years

International
Ensures the timeliness and quality of study deliverables in accordance with SOPs, ICH/GCP guidelines and local regulations
industry
Biotech/Pharma
experience
5 - 7 years

Pleasanton, CA
Maintains collaborative relationships with external partners including regulators and external suppliers.
industry
Financial Services
experience
Less than 5 years

Waltham, MA
Assists in implementing and maintaining various departmental guidelines, procedures and templates associated with the regulatory document management system, regulatory information system, and electronic submissions.
industry
Healthcare IT
experience
Less than 5 years

New York, NY
Focus on compliance best practices with respect to governance, industry initiatives, and effective supervision. Be responsible for enhancing the Firms governance and policy framework to promote compliance awareness and encourage issue escalation.
industry
Financial Services
experience
8 - 10 years

Ogden, UT
Acts as a liaison with the relevant groups and organizations. Researches information for responding to various questions or requests for information from groups including the FDA and other company departments. Prepares all the necessary forms and completes the response documentation according to the required specifications.
industry
Healthcare IT
experience
Less than 5 years