Clinical Scientist. 6-month contract. Onsite in Pomona, CA. We are seeking an experienced Chemist or Toxicologist to join our Analytical Chemistry group in Pomona. This role is ideal for a hands-on scientist with a strong background in LCMS method development and validation for drug testing applications. Key Responsibilities. Develop LCMS test methods for drugs of abuse detection in oral fluid and urine samples. Perform test method characterizati...
Clinical Scientist Role. This role is a 12-month contract with the potential to extend. The position will be based onsite in Clark, NJ. We are seeking a scientist to perform clinical studies in support of our clinical innovation programs related to skin biology. Key Responsibilities. Under the supervision of a clinical project manager, conduct clinical studies to support our clinical innovation programs. Assist the clinical team in various aspect...
Clinical Scientist Role. This role is a 12-month contract with the potential to extend. The position will be based onsite in Clark, NJ. We are seeking a scientist to perform clinical studies in support of our clinical innovation programs related to skin biology. Key Responsibilities. Under the supervision of a clinical project manager, conduct clinical studies to support our clinical innovation programs. Assist the clinical team in various aspect...
Summary. Our client. a Fortune 500 Pharmaceutical Company. has engaged GForce to provide a Project Controls Director who will be reporting. to the Program Director. The Project Controls Director (“PCD”) shall lead aspects of the Project Controls Program including the tracking, management and reporting on the financial performance of capital projects including the Tarrytown Campus Expansion Project. Working with the Program Directors, the Project ...
Summary. Our client. a Fortune 500 Pharmaceutical Company. has engaged GForce to provide a Project Controls Director who will be reporting. to the Program Director. The Project Controls Director (“PCD”) shall lead aspects of the Project Controls Program including the tracking, management and reporting on the financial performance of capital projects including the Tarrytown Campus Expansion Project. Working with the Program Directors, the Project ...
Summary. Our client. a Fortune 500 medical device company, has engaged GForce Life Sciences to provide a Clinical Project Manager who will report directly to the Senior Manager, Project Management. The Clinical Project Manager will provide project management expertise throughout the development and implementation of clinical studies. Interacts with various study support groups and the business unit in order to assist in clinical strategy, the dev...
Scientist I. 12-month Contract. Onsite in Clark, NJ. Responsibilities. Under the supervision of a project leader or a senior scientist, perform laboratory. work to support scientific discovery programs related to skin biology. Conduct in vitro experiments on 2D cells, 3D reconstructed skin or ex vivo human. skin. Micro-dissection of human skin biopsies. Conduct immunohistochemistry experiments and biological assays. Work cross functionally with a...
Position Summary. The Global Product Quality Coordinator supports the Global Quality organization by coordinating supplier quality activities, audit programs, and quality systems. This role ensures compliance with internal standards and regulatory requirements through effective scheduling, documentation, and cross-functional collaboration. Key Responsibilities. Support the Global Product Quality – Supplier Quality Team in inspections, audits, and...
Job Title: Senior Design Quality Engineer. 4-month Contract. Onsite in Newton, MA. Job Overview. We are seeking an experienced Senior Design Quality Engineer to support new product introduction efforts for complex electro-mechanical medical devices. This individual will play a key role in ensuring product quality and regulatory compliance throughout the design and development process. Key Responsibilities. Act as the Quality representative for cr...
Consultant, Clinical Reimbursement and Pricing Specialist, Medical Devices. Summary. Our client. a Fortune 500 medical device company. has engaged GForce Life Sciences to provide a detail-oriented and knowledgeable Clinical Reimbursement and Pricing Specialist to support the pricing and contracting process by triaging and resolving lower- to mid-level pricing deviations and related issues. The ideal candidate will have 2–4 years of experience in ...
Computational Scientist. 18-month contract. Onsite in Lexington, MA. Key Responsibilities. Design and implement unsupervised and supervised machine learning models to identify patient subtypes and treatment-relevant disease endotypes. Integrate and analyze multi-modal omics datasets (particularly proteomics: Olink, SomaScan, LC-MS) with clinical and phenotypic data. Collaborate with cross-functional teams to interpret and translate data insights ...
Clinical Quality Associate. 12-month contract. Hybrid in Princeton, NJ - onsite on Wednesday. Responsibilities. Shadow and support quality oversight activities for 10 ongoing clinical studies (from planning to reporting stages), ensuring best practices are identified and followed. Partner and communicate with Clinical Managers (CMs) and Functional Area (FA) stakeholders to provide cross-functional team support and attend project/study-level meeti...
