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R & D Jobs in New Jersey

1000+ jobs

Description A part time clinical laboratory director is needed for a Physician’s Office Laboratory. The laboratory director must be qualified by CLIA/CLIS to direct high complexity testing in the general immunology and routine chemistry specialties. Duties The laboratory director is responsible for the overall compliance of the laboratory with federal and state guidelines. This includes: Revie...
- Processing a high volume of samples in an analytical laboratory that supports a team of PhD's in R&D and Product Development - Performing sample analysis utilizing titrations and physical property testing - Executing functions of the job in accordance with established procedures _cc_ xsysjscx _cn_ Joule Scientific _rfc_ 157612983...
Seeking a Clinical Research Coordinator for a contract working in East Hanover, NJ Duties: •Assists clinical trial leader or may act as clinical trial leader in the management of individual clinical trials. •Under the direction of the clinical trial leader or clinical research manager, conducts day-to-day activities including protocol writing, trial administration, report writing and interactio...
JOB SUMMARY Provide accurate and timely testing of raw material samples as assigned. Support the production schedule and to ensure the safety and reliability of products produced in compliance with quality and regulatory requirements. Reports to the Raw Material Supervisor ESSENTIAL FUNCTIONS Perform QC testing of raw material samples as assigned by the supervisor as follows: ¯ Proficiency wi...
We have an immediate position for a “eTMF Specialist” with our top pharmaceutical client, if you are interested please send your updated resume to greg @ collabinfo.com orcall me at 732-788-3483 Title: eTMF Specialist Duration: 8+ Months Location: Princeton, NJ Essential Job Duties: · Function as Designated Project Team Member to whom a lead data manager may delegate eTMF-related tasks. · Sc...
Title: Clinical Trial Manager (CTM) Location: Hampton, NJ Duration: 6-12 months Start Date: ASAP Summary Of Position: The Clinical Trial Manager (CTM) is responsible for the oversight and management of all clinical operational activities at the trial and site level for assigned clinical projects. The CTM leads internal cross-functional teams and manages the Sponsor relationship with vendors a...
We currently have an excellent opportunity for a Packaging Engineer located at our Princeton, NJ location. The individual will conduct packaging development projects from initiation through manufacture (launch). Projects will consist of modifications of packaging for existing products as well as the packaging for new products. The individual will be responsible for meeting timelines, finding sol...
Requirements: -Bachelor’s in life sciences or related field -At least 3 years’ experience in as Study Start-Up Specialist or equivalent role Responsibilities: 1. Delivers Business Results -Collect Essential Documents for assigned studies in startup -Maintain Essential documents and updates for ongoing studies (1572, PI CV, Financial Disclosure, Protocol Signature Pages, etc. ) -Execute stud...
Clinical Program Manager Beta Pharma, Inc. is seeking a strategicClinical Program Managerto develop and manage our Clinical projectsin a global capacity. This role is intricate to the overall business development and will report to the Executive Director of Pharmaceutical Development. Beta Pharma, Inc. is an emerging specialty pharmaceutical company dedicated to the discovery, development and co...
RESPONSIBILITIES Design and Optimization of Manufacturing Process for Tablets and Capsules under guidance. Manufacturing of Exhibit batches for ANDA Submission. Technology Transfer of ANDA Products under guidance. Manufacturing of Site Transfer Exhibit Batches for filing purpose. Manufacturing and Packaging of Process Validation batches under guidance. Support production in trouble shooting....
Job Number: 435706 Sr.Site Start-Up Specialist OVERVIEW The Site Start-Up Specialist is responsible for executing study start-up for assigned protocols with the goal of meeting study start-up timelines. Monitor project plans to meet Site Initiation Readiness at the Investigator Meeting. Ensure the accuracy and quality of deliverables from clinical team and vendors. Maintain project metrics and...
TRACKWISE QUALITY OPERATIONS MANAGER REQUIREMENT #16-00216 RECRUITER: CINDI PISNOY JOB LOCATION: NEW BRUNSWICK, NJ FEBRUARY 3, 2016 *** CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 *** Project Description: Will be reviewing and approving process and protocols, not writing them. Review and approval of technical transfer documentation including process, packaging, cleaning, equipm...
A cutting edge specialty pharmaceutical company near East Windsor, NJ that develops and manufactures high dose medications using cutting edge technology to revolutionize how medications are administered, is looking for QUALITY CONTROL CHEMIST. REQUIREMENTS FOR QUALITY CONTROL CHEMIST BS in Chemistry, Biology, Biochemistry or related degree concentration Minimum 4-5 years of experience in QC lab...
We currently have an excellent opportunity for a Flavor & Fragrance Development Associate located at our Princetoon, NJ Location. The Flavor & Fragrance Development Associate support the creation, testing and delivery of high quality, cost effective, consumer delighting flavors and flavors for all CHD categories. Where appropriate, this includes both the perceived and technical performance of the...
Clinical Trial Assistant Requirements: -Associate degree -1-2 year relevant experience in pharmaceutical industry or CRO -Experience supporting clinical trials preferred Responsibilities: -Supports the Clinical Trial Management/operational study teams in the execution and delivery of studies -Support study feasibility activities and perform database/web searches for sites as needed. Work cl...
Responsibilities: Excellent employment opportunity for a Clinical Research Project Manager II in the Raritan, NJ area. Assist Global Regulatory Teams/Global Regulatory Leaders (GRT’s/GRLs) in determining resource requirements utilizing scheduling and resource management tools to support drug development teams without a dedicated RPM in R&D. Creates project and portfolio level reports utilizing ...
Required Skills: HPLC, GC/VIS, GMP Please note that this is a 10 month contract. Summary and Expectations The Analyst executes analytical stability testing of Drug Product according to testing schedules in a productive, compliant and efficient manner using laboratory equipment that is within calibration. HPLC/ UPLC and Dissolution testing are most frequently performed however, other wet chemist...
Pearl Therapeutics, a wholly-owned subsidiary of AstraZeneca, is a growing, dynamic company focused on developing inhalation combination therapies for the treatment of highly prevalent chronic respiratory diseases, including chronic obstructive pulmonary disease (COPD) and asthma. Pearl is seeking to hire individuals that bring energy and passion to deliver the medicines that provide patients and ...
GENEWIZ is a leading global genomics service company and trusted provider for DNA sequencing, gene synthesis, molecular biology, next generation sequencing, bioinformatics, and GLP regulatory services. From the company’s founding, GENEWIZ has maintained its unwavering commitment to providing customers with the best value. Excelling in both science and customer support, GENEWIZ is dedicated to acc...
Theradex® is an international contract research organization providing complete professional services for the clinical research and development of pharmaceutical compounds, medical devices and diagnostic test in the areas of oncology and life-threatening diseases for over 30 years. Theradex® conducts studies which lead to marketing approval of significant advances; and has built a reputation on as...