Biotech, R&D, Science category jobs in New Jersey

Executive Director, Clin Dev & Med Affairs: Exciting Neurology-focused Biopharma – NJ/NY Metro Area [RETAINED SEARCH] Cornerstone Search Group has been retained by a very attractive Neurology focused Biopharmaceutical Company with fast-growing sales, an exciting diverse pipeline, and a rising stock price to help them fill a key Executive Medical Director role. This is a highly visible position tha...
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Sr. Director, Global Drug Safety - build out new global capabilities for Global Pharma (Northeast New Jersey) Summary: Cornerstone Search Group’s Drug Safety practice is working with a successful global pharmaceutical company highly regarded for its R&D capabilities that is now building out a new global drug safety, PV, and risk management organization. This is an opportune time to join this growi...
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Job Description Manage projects/engagements delivering sales, marketing and managed markets solutions to Pharmaceutical clients as well as clients from other Industry verticals such as Retail, Financial Services, Supply Chain etc. Function as trusted delivery leader for key Axtria client engagements. Make presentations and recommendations to clients such as marketing, sales and operations executiv...
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Medical Director, Drug Safety: Exciting & Growing Top 20 Biopharma Co., NJ Summary: Our client has a new opening for a Medical Director, Drug Safety who will be responsible for leading the pharmacovigilance strategies for various compounds in development. This person will utilize their drug safety and clinical development experience to ensure effective collaboration across development teams. This ...
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Clinical Research & Development Leader (Oncology)- Parsippany, NJ Area; Successful & Growing Pharma Summary: Our client is a global leader in the pharmaceutical industry. They develop products for a broad range of therapeutic areas including oncology and have an extremely attractive pipeline in multiple therapeutic areas. They have experienced very strong and steady sales growth and are consistent...
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Executive Medical Director (Physician) -Dermatology Clinical Development–Top 5 Global Pharmaceutical Industry Leader-Develop Novel Dermatology Treatments [RETAINED SEARCH] Position Summary: A challenging position that will lead Global Clinical Development of new/novel Dermatology treatments. This Top Global Pharmaceutical Industry Leader is (and has been) making a major investment in their Dermato...
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Vice President, Quality; NJ Biotech; Retained Search The Vice President, Quality is responsible for all Quality functions, including Quality Assurance, Quality Control, Analytical Services, Quality Compliance, and Validation at both the corporate and Manufacturing sites and oversee a team of 200+. Quality Assurance defines, implements, and manages the various quality programs needed to ensure comp...
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Manager, Pharmacovigilance- Business Site - Florham Park, NJ Area Function Generic Research & Development. J Job Description: Pharmacovigilance Manager implements departmental surveillance strategies in proactive and systematic detection and evaluation of new safety signals and emerging trends from pre and post-marketing safety data. These activities include the evaluation and use of novel and com...
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Consider joining Eurofins Lancaster Laboratories where people are the most important element in our chemistry. Celebrating over 50 years of service, Eurofins Lancaster Laboratories is a leading contract lab providing testing and research services in the environmental, pharmaceutical, and biopharmaceutical sciences to clients worldwide. Eurofins Lancaster Laboratories, a nationally recognized labor...
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We are looking for a highly motivated senior level Director to work closely with key clinical personnel to optimize preclinical strategies focused on pharmacodynamic and predictive biomarkers. Shall: * Generate strategies utilizing your expertise in cancer signaling pathway biology * Drive the discovery of biomarkers related to molecular mechanism of action, pharmacodynamics and predictors of resi...
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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 th...
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Sr. Study Manager 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 Celgene SOPs/WPs. • Sharing best practices • Contributing to process improvement initiatives Study Manager Responsibiliti...
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Job Responsibilities: The Bioinformatics Data Manager will have primary responsibility for the Bioinformatics data lifecycle. S/He will actively manage data exchange with collaborators, leverage both community data and data standards for internal use and develop/adopt/utilize common ontologies to categorize data. S/He will ensure data integrity and the consistency of meta-data across scientific sy...
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Pharmaceutical project manager A Chinese pharmaceutical R&D company, located in Jiangsu Province, China, is looking for a project manager with international pharmaceutical industry experience. Potential candidate should meet following qualifications and job requirements: 1. College or advanced degree from a Chinese university in pharmaceutical sciences, industrial pharmacy, biomedical engineering,...
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Global pharmaceutical company is seeking a Director of Quality. In this critical role, you will head all quality operations for GMP manufacturing. We are looking for a forward thinking quality professional to maintain and build upon our “quality first” approach to providing pharmaceuticals. The Director of Quality is responsible for the site’s quality systems ensuring the connection with manufactu...
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VP (Head), Regulatory Affairs - Global Mid-Sized Pharma – RETAINED SEARCH (North NJ) Summary: Cornerstone Search Group has been retained by a mid-size pharmaceutical company that is going through pipeline growth. As Vice President of Regulatory Affairs, you will be the most senior regulatory person in the company, tasked with transforming the Regulatory function into a world-class “center of excel...
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Head of Biometrics (Manage Department), Growing Global Pharma - New Jersey [RETAINED SEARCH] Summary: Cornerstone Search Group has been retained by a successful global pharmaceutical company renowned for its R&D capabilities that is further expanding its global clinical development and commercial footprint here in the US. In this position, you will lead the Biometrics department (i.e. Biostatistic...
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Director/AD, Head of Clinical Outsourcing (Manage Team): Growing Global Pharma, New Jersey [RETAINED SEARCH] Summary: Cornerstone Search Group has been retained by a successful global pharmaceutical company renowned for its R&D capabilities and is further expanding its global clinical development capabilities and commercial footprint here in the US. This is an opportune time to join this growing e...
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Director / Senior Manager Regulatory Affairs Post Marketing Basic Responsibilities: · Represent Regulatory Affairs on Promotional Review Committee · Act as the primary point of contact with OPDP · Handle BLA/NDA post approval FDA responsibilities · Oversee Clinical from a Quality perspective Job Requirements: Knowledge and Skills Required: · Minimum 5 years of regulatory affairs post marketing exp...
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Associate Director Regulatory Affairs Advertising and Promotions My client recently had one of their two programs approved in January 2013! They have doubled their headcount since in the last ten years to over 300 employees. Their youthful energetic leadership team is seeking an Associate Director of Regulatory Affairs Ad/Promo to help them reach their solid vision! As the Associate Director you w...
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GENERAL DESCRIPTION: Supervise and assist in the conduct of regulatory studies performed at Product Safety Labs (PSL). Responsibilities include: Supervise study conduct. Assist in protocol development, design and implementation. Responsibilities as stated in GLP regulations. Data interpretation and report writing. Client liaison. QUALIFICATIONS: M.S. degree in Chemistry with at least 5 years relat...
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Director, Quality Assurance Systems: Growing and Cutting-edge Biotech, NY/NJ area Summary: Our client is a highly attractive and innovative globally traded Biotech Company working on truly cutting-edge therapeutics that would be first-in-class treatments. They are currently seeking a seasoned QA professional to come in and lead their QA Systems function. This ground-floor opportunity offers a best...
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Requirements: -Doctorate degree -6-9 years experience Responsibilities: -Provide the medical and scientific expertise in designing, assessing and interpreting clinical studies and data as well as additional external medical and scientific information which can be translated and used in commercialization activities including development of clinical claims, advertising claims, promotional claims and...
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