eBay Classifieds  » Jobs » Biotech, R&D, & science » 1-50 of 52 ads in Northern NJ

A fast growing company manufacturing and supplying cosmetic fine chemicals to global brand names such as Estee Lauder, L'oreal, etc is hiring an entry level chemist requring a 4-year college graduate degree or a graduate with a master degree in chemistry. Salary $35000 to $50,000 with standard benefits. For more company information, go to www.grantinc.com. Send your resume to [email removed].  

Location: Woodcliff Lake, NJ Job Title: Clinical Study Manager Duration: 1 year Job Responsibilities: • The Study Manager will be accountable for the overall management of all clinical studies. • Must be comfortable collaborating with other functional teams to coordinate the development and finalization of key study documents including protocols, case report forms, informed consent documents, study management plans and final clinical study reports. • Responsible for monitoring studies against defined ...

Location: Woodcliff Lake, NJ Job Title: Clinical Research Scientist Duration: 1 year Job Responsibilities: • Looking for a clinical research scientist with experience in the pharmaceutical industry. • Assist in the planning, implementation, managing, and reporting of Phase I-III clinical studies • Preparing project and study documents including clinical trial protocols, clinical study reports, patient SAE narratives, clinical sections of registration dossier documents (ISS, ISE, Investigator ...

 Job Description:   Position purpose (A brief statement indicating the basic purpose of the position) This position reports into Head of Global Sourcing Area and works within Procurement across legal entities and national boundaries with a strong focus on procurement strategy and service delivery.  This position would provide contract support within a therapeutic or division specialty. This position will also support the identification, selection, and management of suppliers and contracts across the ...

Excellent opportunity for an experienced Study Builder Designer! Work with a very stable, fast-growing pharmaceutical company! Great work environment! Long-term contract opportunity! Title:  Study Builder Designer Analyst/Project Analyst  Project description: • Work with clinical teams in the development and support of Global Clinical Data Management Systems including planning and coordinating database design, development, implementation, maintenance, and user support of clinical study ...

Great opportunity for an experienced Clinical Data Analyst! Excellent work environment! Long-term contract opportunity!  Project description: • Prepare SDTM Mapping, Program for SDTM SAS datasets creation and Define.xml and related program validation for statistical analysis, tables & listings, and regulatory submissions. • Prepare or participate in creation of SDTM annotated CRFs/eCRFs. • Develop standard Macros and generic SAS programs Libraries including testing and related documentation. ...

 Great opportunity for an experienced Clinical Data Manager! Excellent work environment! Long-term contract opportunity! Title:  Senior Clinical Data Manager, Oncology Project description: -Project Data Management level. Assist Associate Director oversee other data managers on a project. -Perform DM activities for in-house and outsourced trials: protocol review, CRF development, database set up activities, data validation process (including manual data review of listings), SAE reconciliation, ...

Job Summary: Provide support to the Quality Systems department and operations in order to effectively monitor and maintain compliant item master and ERP systems capable of meeting business needs. Divisional responsibility of administration for systems such as ERP, CAPA and Documentation Systems. Essential   Duties & Responsibilities: - Ensure overall compliance with document control requirements and systems data integrity. Conducts periodic reviews of data contained within GIM, Oracle and various ...

Excellent opportunity to work with a fast-growing pharmaceutical company! Great work environment! Long-term contract opportunity! Description of Services Required: · Support clinical trial design and protocol concept sheet development · Develop protocols especially for statistical section · Participate study related activities and provide statistical support such as safety review, interim analyses for Phase II and III oncology studies, etc. · Develop statistical analysis plan (SAP), create TLG ...

Excellent opportunity for experienced Biostatistician! Very stable, fast-growing pharmaceutical company! Excellent work environment! Long-term contract opportunity! Description of Services Required: • Support clinical trial design and protocol concept sheet development • Develop protocols especially for statistical section • Participate study related activities and provide statistical support such as safety review, interim analyses for Phase II and III oncology studies, etc. • Develop ...

Excellent opportunity for experienced Biostat Programmer! Very stable, fast-growing pharmaceutical company! Excellent work environment! Long-term contract opportunity! Biostat programmer Oncology PCU Main purpose of the job: To support the Biostatistics team by carrying out and overseeing programming activities of statistical programmers and external vendors (as required), and to ensure timely and accurate programming and validation activities for clinical studies. Contributes to the overall ...

Excellent opportunity for experienced Biostatistician! Fast-growing and very stable pharmaceutical company! Excellent work environment! Long-term contract! The client is looking for a self-motivated, PhD or MS statistician with experience in clinical trials who will: • Provide statistical support to protocol; review and provide comment on the study protocol. • Review and approve CCG plan, data cleaning plan, edit checks and data specs for vendor data provided by the data management team, or ...

Serves as Global Program/Brand Team (GPT/GBT) scientific safety leader. Responsible for safety issue management from formation of GPT/GBT through Life Cycle Management (post-approval). Develops and is responsible for key internal safety documents from the formation of the GPT/GBT through Life Cycle Management. Reviews these documents regularly and updates as required (e.g. when significant new information received). Ensures that these, and all other pro­ject-related safety documents, are consistent ...

Key Accountabilites: - Evaluate new materials to support the advancement of Company existing and emerging arket strategies with emphasis on high performance elastomers like silicone and flouroelastomers. - Research new and novel technology advances and trends in materials. - Support sales, product development, and manufacturing in understanding what we can achieve with respect to material science. - Develop new Intellectual Property (IP) for Company. - Access the potential for existing product / ...

  Currently seeking 2 Lead Clinical Data Managers for a permanent opportunity with a leader in the pharmaceutical industry.  Ideally looking for individuals to start as soon as possible.   Responsibilities:   Will lead & manage project activities at the study level for clinical data management and ensure coordination between teams.  Will act as single point of contact for all data management deliverables during study set-up, conduct, and close out phases.   Responsible for the creation/review ...

Job Ref: #1637 Relocation: Yes Location: Parsippany NJ Salary: Dependent on candidate. Summary: Growing environmental consulting firm looking for a regulatory compliance specialist with 10+ Years of experience. We are seeking a professional with project experience to ensure environmental permitting, periodic reporting, training, and other compliance obligations relevant to a specific site are met on a consistent and timely basis. This is a leadership position with technical ...

Responsibilities: • Operationally supports and executes the imaging plans outlined in Oncology study protocols including supply of standard language, management of imaging CROs • Preparation of scope of work, imaging charters, and support imaging data transfer and reconciliation. Skills • Familiarity with a broad range of imaging techniques. • Preferred experience in CRO management or CRO environment, and an understanding of Imaging CRO capabilities. • Basic knowledge of clinical ...

Description: The Clinical Scientist is responsible for the scientific strategy of assigned clinical trials for protocol development, ensuring the review/reporting of quality trial data, and study reporting/publishing in compliance with client’s processes, GCP/ICH and regulatory requirements. Supports program level activities as assigned. Program/project level responsibilities: • Support the development of operational plans for clinical deliverables, effectively applying principles of design ...

Job Description: Support the operational execution of the clinical study strategies related to biomarker and pharmacokinetic assessments in oncology protocols, in compliance with client’s processes and regulatory requirements and in collaboration with Oncology Clinical Teams. Responsibilities: • Sample tracking for biomarker and pharmacokinetic samples from clinical site to analytical laboratory. • Setting up the laboratory procedures, being the primary point of contact and providing ongoing ...

Responsibilities: • Leads Global Medical Affairs strategy and implementation for specified compound(s). • Acts as medical representative on the Global Brand Team, Global Project Team, and International Clinical Team • Provides clinical leadership and accountable for global medical affairs strategy and life cycle management • Acts as clinical lead for Scientific Communication deliverables and publications (with Scientific Affairs group), brand-related input into therapeutic area and disease area ...

Responsibilities: • Working with Clinical Science/Business Units and a Standard Governance Board, the successful candidate will transform data collection requirements into data models. • Provide input to OC Global Librarian team in developing and maintaining standard objects for OC standard Global Library. • Work with the Clinical Science Units to understand the data requirements for their reporting, submission and collection • Model the data collection , storage, transformation & submission ...

 Job Responsibilities: • Guide planning, evaluation and interpretation of early clinical development studies with the goal of influencing key drug development, regulatory and therapeutic decisions. • Proactively initiate and conduct clinical trial simulations and  pharmacometric modeling to support decision making and quantitative exploration of pharmacological principles. • Proactively implement translational medicine strategies and statistical methods into area of responsibility. ...

Bachelor’s Degree in a technical discipline plus more than 10 years of applicable technical and/or management experience,Extensive experience with polyurethane rigid foam technology, processing, and applications, including production, formulating, and testing,Demonstrated ability to lead people, manage performance, and develop talent in technical organizations,Demonstrated strong communication skills for interacting with all levels of personnel, supporting department objectives and management ...

Global Clinical Project Manager Oncology experience is a PLUS! 10+ years in clinical industry 2+ years in project management  

Contact Dan at 815-756-1221 Qualifications: - BS/MS Food Science - 5+ years food product development experience - Experience in formulation and manufacturing of food products - Understanding of FDA GMP's - Skilled in sensory evaluation - Ability to travel internationally and domestically - Analytical and problem solving skills - Excellent interpersonal and communication skills - Computer literate and experienced in fundamentals Responsibilities: - Develop new and existing food products - Coordinate ...

::Contact Jeff for more details at 815-756-1221. Attach resume when responding to this posting - Please only contact if you meet the listed qualifications:: The Sr. Director will be responsible for for technical and innovation aspects of new product and process development. Will make technical recommendations to upper management. Will work closely with other business units including Marketing, R&D, Supply Chain, and technical management personnel. Qualifications: - BS/MS Food Science, Engineering, ...

  Order #: 90692 Title of Position:  Sr. Study Manager Company: InVentiv Health Clinical Location: City/State:  Summit, NJ Zip Code:  07901 # of positions: 3 Contract Length:  12 Months    ** LOOKING FOR STUDY MANAGERS OR SR. STUDY MANAGERS The Study Manager is responsible for • Leading one or several cross functional study teams (and/or sub-teams) to deliver clinical research studies on time, within budget and with good quality in compliance with Regulatory Authorities regulations/guidelines and ...

Location Woodcliff Lake, NJ Duration 1 year Job Responsibilities • Can work remotely but must work 2 days onsite/week. • Work directly with clinical study teams, the Neuroscience medical writing teams, regulatory affairs personnel, and the publishing group in the preparation of scientifically valid regulatory documents. • Responsibilities include prepare regulatory documents on behalf of client in accordance to ICH guidelines, international regulations, client standards ...

Seeking a strategic expert in the respiratory disorder field with a successful track record planning and managing all preclinical activities of novel protein therapeutics and establishing pharmaceutical and academic collaborations. Shall manage a team of up to 10 scientists in target discovery, biomarker development, antibody generation, mechanism-of-action studies, and in vitro & in vivo models. Requires PhD and 10+ years of respiratory biology experience. Enjoy the career path opportunities ...

JOB SUMMARY:   The Clinical Study Coordinator will work with Project Leaders/Sr. Project Leaders (PL/Sr. PL), Clinical Research Associates (CRA) and Directors to fulfill activities in support of one or more clinical trials in compliance with applicable regulations and standard operating procedures.  The Clinical Study Coordinator will also perform routine regulatory document preparation, distribution, receipt, inspection and tracking for assigned clinical trials.  ...

Contact Kristine at 815-756-1221 Qualifications: - MS/PhD Nutrition or related field - Registered Dietician preferred - 10+ years experience in the applied nutrition and health field - Able to leverage the scientific knowledge between nutrition and marketing - Strong understanding of other regulations - Strong leadership skills - Excellent communication skills Responsibilities: - Manage 2 direct reports to support health and wellness programs and innovations - Lead the identification and ...

Representation of GLF on cross-functional Project Teams (early or full development) under appropriate guidance; responsible for design and co-ordination of pharmacokinetic ele-ments of preclinical and/or clinical development plans and regulatory documentation; assures that the pharmacokinetic support to all assigned projects is optimal in quality, timing and cost; ensure appropriate input to the early development team and/or later stage teams; evaluates in-licensing opportunities upon request and is ...

Successful medical communication agency in N NJ, focused on publication planning and execution, is seeking a Sr. Medical Writer/Scientific Specialist with strong Oncology experience, to join their team.   The Sr Medical Writer/Scientific Specialist  provides senior therapy area/content expertise and leads the delivery of assigned programs/projects within account team, interacting directly with client and KOLs.   The company offers a generous salary and some work from home flexibility.  Local ...

Successful  Medical Communication agency focused on publication planning and execution for pharmaceutical clients seeks a Publication Planning Program Specialist to be responsible for the day-to-day management of assigned publication plan, delivery of outputs, financial tracking and meeting activities, working closely with all members of the delivery team across departments.  This is an on-site, stafff opportunity in Hackensack, NJ with occasional travel.  Excellent salary, benefits.  No relocation, ...

This successful, large pharmaceutical with marketed products and deep pipeline is seeking a highly skilled writer to write high-level regulatory submission documents and manage the submission process.   Excellent Salary, bonus, benefits, and relocation assistance offered for US-based candidates. The Oncology Submission Mgr. will plan and coordinate tasks supporting the timely delivery of high quality documents for sNDAs/Type II Variations or non-complex NDAs/MAAs to Health ...

Highly successful Medical Communication Agency in N NJ/NY area seeks Scientific and Editorial Director with previous medcom agency and publication planning experience for pharmaceutical clients.  Excellent compensation and bonus offered.  2 days work from home possible.   Seeking local candidates only as no relocation is offered. Responsibilities include:   *  Running department of 30 people (6 direct reports) including Scientific Team Leads, Editorial Mgrs, Scientific Specialists and Writers, ...

  Sr. Medical Writer or Expert Medical Writer - Regulatory submissions – Northern New Jersey   Job Description : Top N NJ pharmaceutical with marketed products and a deep pipeline seeks staff Sr. or Expert Regulatory writer to write, edit and manage the production of high quality clinical documentation for submission to regulatory authorities in support of marketing applications, and to provide authoritative documentation-related consultancy to other line functions.  The company offers an excellent ...

Contact Jeff for more information at 815-756-1221 Qualifications: - BS Food Science, Chemical Engineering - 1-3 years of food product development experience - Familiar with manufacturing processes and equipment - Technical competence - Time management skills - Basic understanding of the sciences and food recipes - Computer skills - Communication and interpersonal skills - Working knowledge of plant processes and facilities - US Citizen or Perm Resident Responsibilities: - Execute tests using ...

Responsibilities: • Facilitate the activities required to assess External Service Providers (ESPs) in support of a robust supplier risk management program. • The scope includes current ESPs responsible for the performance of Phase I-IV clinical trial activities. This would include the evaluation of defined due diligence criteria across a specific supply base. • Function as Subject Matter Expert (SME) in assessing vendor quality, compliance, and risk. • Ensure consistent implementation and ...

Leads Global Medical Affairs strategy and implementation for specified compound(s).Acts as medical representative on the Global Brand Team, Global Project Team, and International Clinical TeamProvides clinical leadership and accountable for global medical affairs strategy and life cycle management Acts as clinical lead for Scientific Communication deliverables and publications (with Scientific Affairs group), brand-related input into therapeutic area and disease area strategies. Provide medical ...

  Seeking a CDM to work for a mid-sized CRO in NJ.  Responsibilities include:    ·         Provide Clinical data management support to Clinical Operations team and/or study project, Clinical Data Management team and Biostatistics.   ·         Participates in the review of Clinical research documents (eg. protocols, CRFs Reports and Statistical analysis, Develops Data Management Plan (DMP), maintains DMP throughout lifecycle of study project and ensures DMP is followed according to study ...

Contact Kristine at the phone number listed. Key responsibilities include the following: Ensure regulatory compliance of products, labels, advertising and promotions as well as adherence to policies and guidelines • Manage and develop staff and oversee contractors • Interface across the Snacks and Beverage businesses and with corporate functions to provide the nutrition/regulatory perspective and ensure projects are effectively advanced • Support implementation/tracking of corporate health & ...

Description This position supports our Home Appliance Division in the USA by providing an independent performance assessment. As team lead, the role of the consumer scientist is to coordinate and evaluate home appliances, such as ranges, MWO, refrigerators, laundry, dishwashers, vacuums, and AC, to specialized test conditions in order to determine our competitive edge, how to improve product, and document findings based on product performance using industry protocols. This also entails ...

Description This position supports our Home Appliance Division in the USA by providing an independent performance assessment of new models based on external reviewer’s protocols and supports R&D product development. This role continuously evolves by updating and creating new testing methods and supports assigned product categories. The position is based in Pine Brook, NJ. Duties & Responsibilities • Conduct competitive benchmark performance testing to industry protocols and procedures for ...

CYTOTECHNOLOGIST • Correctly match the slide number with the appropriate requisition form • Use the clinical history and other patient information in arriving at the proper diagnosis for each nongynecologic and gynecologic cytological specimen • Examine cytology specimens for the presence of abnormal cellular changes & pathogens • Evaluate and mark reactive, abnormal or questionable cell(s) for Pathologists’ review • Record cell findings in Renaissance for follow-up review and evaluation by the ...

Contact Larry at 815-756-1221 Qualifications: - PhD in Chemistry or Analytical Chemistry - Track record of analytical method development and transfer, publications, and patents - hands-on experimental skills in chromatography - Supervisory experience and analytical experience in specialty chemical industry - Good communication and interpersonal skills Duties: - Provide analytical support for new product development, pilot scale-up, manufacturing, applications, R&D, and various business units - Lead ...

Contact Kristine at 815-756-1221 Qualifications: - BS/MS Food Science - 6+ years of successful product & process development experience in snack foods - Strong technical foundation with ingredient functionality from cereal, grains, cakes, etc. - Experience leading programs through the development cycle - Project management skills - Ability to interface with marketing, operations, procurement and regulatory - Excellent communication skills Duties: - Develop new products and processes from bench top ...

Contact Kristine at 815-756-1221 Qualifications: - BS / MS Food Science, Food Engineering - 3+ years in food product development, R&D and Manufacturing - Project management, process development and commercialization experience - Knowledge of snack products and processes is a plus - Proven cross-functional team experience - Strong budget and finance skills - Willing to travel 25% Job Scope: Responsible for development and implementation of productivity opportunities

Contact Kristine at 815-756-1221 for more information Qualifications: - MS/PhD in Toxicology, Science, Nutrition - 7-10 years food ingredient regulatory experience - Food, beverage, dietary supplement or personal care experience required - Familiar with U.S. FDA and other international regulatory agencies - Extensive toxicity knowledge - Knowledge of corporate resources to support objectives - Ability to interface with people at all levels - Demonstrated written and oral communication skills - ...

SENIOR TECHNICAL PROJECT MANAGER (MAHWAH AREA, NEW JERSEY) SENIOR TECHNICAL PROJECT MANAGER POSITION SUMMARY: The Senior Technical Project Manager is responsible for coordinating multi-site development activities through the company's Design Control and Idea to Market process. This includes aligning and setting the project scope and objectives with all relevant stakeholders. He or she is setting and holding the team accountable for deliverable timelines, meeting performance requirements, and ...