Proclinical

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...

Lead global regulatory strategy for a key oncology program in this newly created Director role. Serve as the principal regulatory authority, guiding submissions and product development. This remote position in Germany/UK offers a significant impact on cancer innovation. Expertise in global oncolo...

Join our team in Basel as a Downstream Process Development Expert. You will plan and execute scientific experiments for drug substance manufacturing, focusing on purification techniques like chromatography. This role requires a biotechnology background, lab proficiency, and strong English skills....

Join our team in Basel as a Quality Associate, supporting GMP quality assurance. You will ensure cGMP compliance, manage batch records, and contribute to key projects. The role requires strong regulatory knowledge, excellent English, and EU work rights.

Join a pioneering team in Basel developing life-changing CGM algorithms. Utilize Python and advanced ML (TensorFlow/PyTorch) to transform sensor data into clinical insights. A Master's/PhD in a quantitative field and experience with time-series data are essential. Collaborate in an Agile, multidi...