Proclinical - United States

Join a dynamic team in Tarrytown, NY, to advance microfluidics-powered antibody discovery. This role requires hands-on expertise with microfluidic chips, cell biology assays, and data analysis. Ideal candidates have a bioengineering background and proficiency in Python or MATLAB for system contro...

Join our clinical research team in Moore, USA, as an Unblinded Clinical Research Coordinator. You will manage Investigational Product (IP) accountability and ensure strict protocol compliance. This role requires strong organizational skills and experience in clinical trial operations. Support stu...

Join our Cambridge, US team as a Senior Associate Scientist. You will manage siRNA drug substance/product specifications in a GMP environment. The role requires a Chemistry/Biochemistry degree, cGMP lab experience, and HPLC/oligonucleotide analysis skills. You will author technical documents and ...

Join a leading pharmaceutical company in Lexington as a Research Associate in Injectable Formulation Development. You will focus on formulating and characterizing peptides, proteins, and small molecules. The role requires hands-on lab work, biophysical analysis, and collaboration with cross-funct...

Join our Wilmington-based team as a Research Scientist in Cell and Molecular Biology. Contribute to pioneering cancer drug discovery by developing preclinical models and functional cellular assays. Expertise in stem cell biology, molecular techniques (flow cytometry, CRISPR), and hematologic mali...

Join Proclinical as a Clinical Study Associate in a fully remote role. Support global clinical trial execution, ensuring GCP compliance and data quality. Utilize your CRO or pharmaceutical experience in site coordination and TMF management. This contract position offers impactful work from anywhere.

Lead document quality and submission readiness for a top pharmaceutical firm in Cambridge, US. Utilize your regulatory publishing expertise to manage and QC clinical documents like CSRs and IBs, ensuring eCTD compliance. This role demands sharp detail-orientation and proficiency in MS Office/Adob...

Join our client's dynamic pharmaceutical/biotech team in Norton, MA, as a Quality Control Analyst II. Perform critical HPLC/UPLC and microbiological testing to support product release and stability. Utilize your GMP experience to ensure compliance and contribute to continuous improvement in a lab...

Join our client's innovative team in Lexington, MA, as a DMPK Project Representative. Provide scientific leadership in small molecule drug discovery, integrating ADME/PK strategies. You will design experiments, manage CROs, and collaborate cross-functionally. This contract role requires strong AD...

Lead a patient-first customer service organization in Boston, shaping exceptional support experiences at the intersection of healthcare and innovation. You will build and develop a high-performing team, establishing multi-channel support systems and performance standards. This role requires exper...

Join a leading team in Cambridge, MA, as a Senior Clinical Study Associate. This hybrid role involves overseeing clinical trial execution, TMF management, and vendor coordination. You will ensure regulatory compliance and support site performance. Ideal candidates have strong organizational skill...

Join our Philadelphia team as an Associate Warehouse Coordinator. You will ensure seamless inventory and delivery processes, utilizing SAP and Microsoft Office. This role requires strong communication skills and a commitment to FDA compliance and data integrity. Support warehouse operations in a ...