Proclinical

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 a leading pharmaceutical company in Basel as a Lab Associate in Cellular Functional & Soluble Biomarkers. Design and develop critical biomarker assays (e.g., flow cytometry, ELISA) to support clinical trials in a GxP environment. This role offers a dynamic, collaborative setting for a proact...

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 strategic sourcing for laboratory equipment in Visp, Switzerland. This contract role requires a Bachelor's degree and proven procurement experience in regulated industries. You will manage RFx processes, develop category strategies, and optimize costs for CAPEX projects, with fluency in Engl...

Lead impactful engineering projects in Visp, Switzerland. This contract role requires a proactive Project Engineer with a technical degree and strong leadership skills. You will manage investment projects, optimize processes, and ensure execution within cost and timeline. Fluency in English and G...

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 a dynamic rare disease team as a Key Account Manager aHUS, based in Munich. This field-based role focuses on building relationships with nephrologists and hospital decision-makers to enhance product access. You will identify opportunities, provide educational support, and collaborate cross-f...

Join a leading team as a Senior GMP Quality Auditor in London. You will manage a global, risk-based vendor audit program, ensuring compliance with EU GMP/GDP. This role requires extensive travel, mentoring, and expertise in pharmaceutical quality systems. Apply your auditing skills in a dynamic, ...

Join Proclinical as a GCP QA Consultant in Berlin. You will oversee quality assurance for Phase 2-3 oncology trials, ensuring ICH-GCP compliance and inspection readiness. Your role involves risk management, document review, and collaborating with cross-functional teams to maintain the highest cli...