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
Vacancy posted 3 days ago
Similar jobs that could be interesting for youBased on the Clinical Quality & Regulatory Associate in Springfield, NJ vacancy
- ...Description Job Description Summary: The Quality Associate will perform independent examination (... ...related to the conduct of the clinical trial in different therapeutic areas and... ...Interprets GCP, and associated regulatory documents to facilitate auditing and process...SuggestedTemporary workWork at officeLocal areaFlexible hours
Pinnacle Clinical Research
Springfield, NJ8 days ago $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$27.34 - $41.04 per hour
...General Summary: The Quality Specialist is responsible for... ...collaborating with all areas of clinical operations to assure tissue... ...education activities and meetings associated with organ and tissue... ...with quality standards and regulatory requirements. Performs other...SuggestedHourly payFull timeTemporary workH1bWork at officeLocal areaFlexible hoursNJ Sharing Network
New Providence, NJ3 days ago- 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...SuggestedContract workWork at office
$142.8k - $196.35k
Principal Regulatory Affairs Specialist As a Principal Regulatory Affairs... ...and coordinating associated activities for assigned drug... ...vigilance reporting, and other quality‑related initiatives with minimal... ...activities, including clinical requirements for medical devices...SuggestedRemote jobH1bRelocation packageFlexible hours$70k - $130k
Position Overview The Senior Specialist, Regulatory Operations, will be responsible for submission management across the development pipeline... ...regulatory submissions, ensuring timely, compliant, and high‑quality deliverables. Interface with external publishing vendor(s)...Temporary workWork at officeLocal areaRemote workFlexible hours- ...mission centers on delivering only the best quality talent, the first time and every time.... ...areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Description Title: Regulatory Associate Duration:6 Months (Possibility of Extension...Work experience placementLocal area
- ...POSITION (Position Summary): The Quality Assurance Specialist... ...all activities for routine clinical and commercial product release... ...consistent compliance with regulatory and industry expectations. Assist... ...is preferred. Minimum of Associates degree Experience: • 3-5 years...
- ...Purpose and product of position: The Quality Assurance Label Control Specialist at the... ...and continuous improvement of the clinical and commercial label control process, procedures... ...S-12 facility to ensure patient safety, regulatory requirements and improve its...Work experience placementWork at officeShift workAfternoon shift
Integrated Resources
Summit, NJ3 days ago - Position Summary: The Global Product Quality Specialist will be responsible for... ...documentation and change controls associated with key deliverables to clinical and commercial documentation... ...: Comprehensive understanding of regulatory guidelines. Capable of handling complex...Work 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
$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- ...Wed- Sat (1 pm to 11 pm). The Quality Assurance Document Control (... ...: Bachelor's degree or Associate's Degree with 3+ Years of Experience... ...with FDA or other regulatory agencies strongly preferred.... ...group. Responsible for issuing clinical and commercial in-process and...Shift work
$220.47k - $330.7k
...IDTs), partnering with Scientific Licensing colleagues (SLO) where appropriate; Drive internal opportunity assessments — technical, clinical, commercial and financial — and synthesize findings for BU and executive decision‑making; Negotiate directly with partner...Local area- ...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...
- ...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....
- ...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
- 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...
$133.5k - $192.83k
...Job Title : Global Quality Auditor ~ Location: Morristown, NJ About the Job... ...all GXP audit in areas of current, Good Clinical Practices (GCP), Good Pharmacovigilance... ...Practices. Deep knowledge of global regulatory requirements and standards. Strong understanding...WorldwideSanofi
Morristown, NJ4 days ago- ...Job Description Job Description Title: Regulatory Associate Location: Warren, NJ 07059 (Onsite or 3 days in office - Hybrid) Duration... .../Pharma related industry. ~ Experience and knowledge in Quality, product development and manufacturing areas. ~ Experience...Work at officeDay shift
Lancesoft INC
Warren, NJ16 days ago $30 - $36 per hour
...Job Description Job Description 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...Contract workWork experience placementIntelliPro Group Inc.
Clark, NJ7 days ago- ...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
$50k - $150k
...execution excellence. If you're currently self-generating one or two loans per month (or less) and would rather work inside on quality files than constantly prospect, this position offers stability, leverage, and strong income potential. What You'll Do Take...For contractorsLocal areaImmediate startRemote workKORE1 Technologies
Union, NJ2 days ago- ...Position Summary The Senior Specialist, Regulatory Affairs will provide expertise to the organization in the development of regulatory compliance strategies and in ensuring its conformance to Health Authority requirements. Essential Functions Serve as a Regulatory...Work at office
Avetix Bio
Summit, NJ1 day ago $19 - $20.5 per hour
...ourselves in expertly sourcing the highest quality foods and treating our customers like... ...special. The role: The Quality Assurance Associate (Food Manufacturing) is responsible for... ...quality assurance, food safety, and regulatory requirements by partnering with Operations...Hourly payFull timeFor contractorsSeasonal workImmediate startFlexible hoursShift workNuts.com
Cranford, NJ19 days ago- ...will engage with internal teams and external partners to uphold regulatory standards and drive compliance initiatives. Your expertise in... ...If you thrive in a fast-paced setting and have a passion for quality assurance, this is an exciting opportunity to make a significant...
TechDigital Group
Summit, NJ22 hours ago - An established industry player is seeking a detail-oriented professional to manage external quality control processes. This role involves coordinating with Contract Test Laboratories and ensuring timely release of vector for various programs. The ideal candidate will have...Contract work
- An established industry player is seeking an Associate Specialist for Quality Product Release-Disposition. This role is crucial for maintaining compliance with corporate policies and global cGMP standards. The successful candidate will manage quality records, support batch...
$97.8k - $133.46k
...driving innovations that improve health care quality, affordability, and member experience.... ...by corporate objectives and NCQA and regulatory regulations. Analyzes complex data and... ...external stakeholders to promote HCM&T clinical and operational improvement activities....Live inLocal area- 340B Health in Morristown, NJ, is seeking qualified candidates for a full-time clinical role that involves reviewing and coding documentation for home care. Successful applicants will demonstrate strong knowledge in home care regulations and OASIS. The role includes providing...Full time
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Clinical Quality & Regulatory Associate. Be the first to apply!
