Clinical Quality & Regulatory Associate
Pinnacle Clinical Research
Pinnacle Clinical Research in Springfield, NJ is seeking a Quality Associate to ensure the quality of clinical trials. Responsibilities include performing audits, ensuring compliance with regulations, and training site staff. Candidates should have a Bachelor's Degree in a scientific field and 2-4 years of relevant experience in clinical research. The position offers competitive pay and excellent benefits, with a focus on professional growth in a supportive environment. #J-18808-Ljbffr Pinnacle Clinical Research
- ...The Quality Associate will perform independent examination (i.e., audit) of multiple trial‑related... ...related to the conduct of the clinical trial in different therapeutic areas and... ...inspected Interprets GCP and associated regulatory documents to facilitate auditing and process...SuggestedTemporary workWork at officeLocal areaFlexible hours
- ...The Regulatory Affairs Sr. Associate is an experienced medical device regulatory professional who can independently... ...IFUs, risk management linkages, clinical evaluation inputs, PMS/PMCF linkages... ...regulatory content. Partner with Quality, Clinical/Medical Affairs,...SuggestedWork at office
- WorkLlama, Inc. is seeking a Quality Auditor - Scientific - II in Rahway, NJ. The role involves critical oversight for manufacturing and testing activities in drug production, ensuring GMP compliance. Key responsibilities include quality review of batch records, conducting...Suggested
$70k - $75k
A leading food manufacturer is seeking a Regulatory Compliance Specialist to coordinate product labeling projects... ...documentation. The ideal candidate will have an associate degree and at least 3 years of experience in quality assurance within a food manufacturing environment...SuggestedFull time- ...Position Overview Senior Specialist, Regulatory Operations: Responsible for submission management across the development pipeline and... ...management of regulatory submissions, ensuring timely, compliant, high‑quality deliverables. Interface with external publishing vendors and...SuggestedTemporary workWork at officeRemote work
$65k
...Job Description The Quality Assurance Specialist II, Cosmetics and Hygiene, assists with... ...according to ISO 19011 standards, supports regulatory audits, and remains knowledgeable of... ...standards, including, but not limited to Good Clinical Practices, International Center for...Immediate start$45k - $83.5k
...Job Category: STAFF - CLINICAL OPERATIONS Requisition Number: CREDE006596 Posted : December 3, 2025 Full-Time On-site Salary Range : $45,000 USD to $83,500 USD Locations Showing 1 location NJE Non Clinical CBO New Providence, NJ 07974, USA Description The Credentialing...Full timeShift work- ...Responsible for assisting with laboratory analysis for clinical release and clinical stability testing. Conduct reference standards qualification analyses of developmental and commercial compounds, prototype formulations and finished products in support of clinical testing...
- The Global Supplier Quality, External QC - Vector will process external deviation and change records from our Contract Test Laboratories... ...Quality to release vector in a timely manner for commercial, clinical, and early development programs. REQUIRED COMPETENCIES: Knowledge...Contract workWork at office
- ...Type: Contract Overview The Quality Assurance Label Control (QALC... .... Responsible for issuing clinical and commercial in-process and... ...knowledge of current GMPs and regulatory guidelines. Requirements Bachelors... ...Jewelry Quality Assurance Associate New York, NY $50,000.00-$70,0...Contract workAfternoon shift
- ...staffing agency is looking for a Laboratory Analyst in Summit, New Jersey. This role involves conducting laboratory analysis for clinical release and stability testing. Candidates must possess a BS/MS in analytical chemistry or a relevant discipline, along with 2 to 4...
- ...and share local insight to deliver true global perspectives. Job Description Responsible for assisting with laboratory analysis for clinical release and routine stability testing. May conduct routine release and stability analyses of developmental compounds, prototype...Local areaImmediate start
- ...seeking candidates for a laboratory role in Summit, New Jersey. The responsibilities include assisting with laboratory analysis for clinical release and routine stability testing, conducting analytical experiments and documenting lab work following compliance protocols....
- Credentialing Specialist Shift: 5 Day Shifts X 7.5 Hrs Start Date: 07/13/2026 End Date: 10/10/2026 Duration: 13 Week(s) Location: Morristown, NJ TALENTShift workDay shift
$70k - $75k
...Regulatory Compliance Specialist Base pay range: $70,000.00/yr - $75,000.00/yr The Regulatory... ...specifications, and certifications. The associate also supports regulatory and customer... ...Employment Type Full-time Job Function Quality Assurance and Manufacturing Industries Pharmaceutical...Full timeWork at officeImmediate start- ...compliance of equipment and the ECQ group with local, global, and regulatory guidelines. The incumbent will perform periodic reviews of... ...Excellent computer skills including knowledge of equipment data quality systems. Strong verbal and written communication skills, and...Work at officeLocal area
$70 - $75 per hour
...Compliance Officer and primary resource for regulatory guidance. Develop, implement, and... ...affecting hospice operations. Partner with the Quality team to develop corrective action plans... ...decision‑making. Collaborate with clinical leadership to ensure documentation meets...Hourly payPart time- ...A leading regulatory compliance firm is seeking a detail-oriented Regulatory Affairs Associate I to support compliance activities for products distributed in the United States and Canada. The role involves reviewing product formulas and artwork for regulatory compliance...Contract work
$70k - $75k
...The Regulatory Compliance Associate, in this highly detail‑oriented role, is responsible for coordinating the workflow of domestic and international product labeling projects, maintaining all project documentation, obtaining required approvals, and communicating new and...Full timeWork at office- ...and in writing (English language required). Quality Operations and Systems Support including deviation... ...all-inclusive. Direct reporting line to the Associate Director of the Global Quality Patient Operations and Apheresis Regulatory Vigilance, CTDO. Specific Knowledge, Skills,...Flexible hours
- ...over 3,000 individuals every year. We are excited to announce our Quality Assurance Specialist opening! The Quality Assurance Specialist... ...regulation & accreditation Conduct unannounced inspections and clinical audits of all programs to ensure compliance and conformance....Work at officeLocal areaMonday to FridayFlexible hours
$105k - $150k
...Technologies, Inc. Department: MSFC Employment Type: $105,000.00-$150,000.00 per year Location: Springfield, NJ Responsibilities Perform Quality Assurance Specialist (QAS) inspection functions for space flight hardware in accordance with established customer and company...Full timeWork experience placementWork at officeFlexible hours- ...Overview Job Title: Regulatory Affairs Associate I Location: Clark, NJ 07066 Duration: 06 months Job Profile Summary Maintain competencies in North American (HazCom 2024, WHMIS 2022) and European (CLP) hazard communication requirements. Assess, classify and author safety...Local area
- ...requirements. Review raw materials and associated toxicology/ecotoxicology information to... ...communication and transportation data accuracy and quality. Assist in review and update of SDS from... ...inventories and lists for populating regulatory information section of SDS. Maintain...Contract workWork at officeLocal areaRemote workShift work
$30 - $36 per hour
...Job Title: Regulatory Affairs Associate I Position Type: Contract (12+ Months) Location: Clark, NJ 07066 Salary Rate: $30–36/hour Job Description We are seeking a detail-oriented Regulatory Affairs Associate I to support regulatory compliance activities for products distributed...Contract workWork experience placement$29.42 per hour
...Overview The Fountain Group is currently seeking a Regulatory Affairs Associate I for a prominent client of ours. This position is located at Clark, NJ. Pay Rate: $29.42/Hour Duration: 6 months Shift Details: Hybrid is dependent upon candidate engagement, reactivity,...Shift work- ...The Compliance Coordinator is responsible for supporting regulatory compliance operations for Huber Winery, Starlight Distillery, and... ...accurate, and compliant with federal regulations. Qualifications Associate’s or Bachelor’s degree in Business, Accounting, Compliance,...Work at officeLocal areaMonday to Friday
$250k
Paramount Residential Mortgage Group Inc. (PRMG Inc.) is seeking an experienced professional for mortgage loan processing in Union, New Jersey. This role involves verifying application information, advising clients on home loan options, and reviewing loan files for compliance...- ...Liaison between Employee/Candidates, Providers and internal clinical staff as required Reviews and verifies applicable invoices.... ...Experience, And Qualifications High School Diploma/GED required, Associates Degree in a healthcare related discipline required. Experience...Work at officeFlexible hours
$1,363.71 per month
...Details Client Name Atlantic Health System Morristown 07960 Job Type Travel Offering Non-Clinical Profession Non-Clinical Specialty Credentialing Specialist Job ID 18520720 Job Title Credentialing...Weekly payShift workDay shift
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