Proclinical - Remote work

Regulatory Affairs Contractor sought in Maidenhead, UK, to lead EU and MENA regulatory strategies for rare disease products. This role requires a degree in Science, deep knowledge of European regulations, and experience with product registration in the Middle East, Africa, and Russia. You will ma...

Seeking a Director/Senior Director, GCP Quality Assurance Lead in Boston to oversee clinical trials in neurology and rare diseases. This role requires extensive GCP QA experience, regulatory inspection leadership, and expertise with eTMF systems like Veeva Vault. You will ensure compliance with I...

Drive growth within the UK’s Golden Triangle life sciences hub as a Business Development Executive. This remote role targets biotech and pharma companies, focusing on oncology and contract manufacturing. You need a science degree and proven success in CRO/CDMO or pharma services. Join Proclinical...

Seeking an experienced Clinical Research Site Manager in Midlothian, USA. Lead daily site operations, ensure regulatory compliance, and drive study performance to meet client goals. This role requires proven industry experience and strong leadership skills to manage staff and optimize recruitment...

Lead clinical science for transformative rare disease studies in Boston. This senior role requires a strong scientific background and experience in pharmaceutical drug development. You will design and execute clinical research while ensuring regulatory compliance. Collaborate cross-functionally t...

Join an innovative commercial team in Germany as a Multiomics Sales Specialist. Drive revenue by promoting cutting-edge genomics and proteomics solutions. This Berlin-based role requires expertise in multiomics, fluency in German/English, and 50-60% travel. Be a trusted consultant, advancing scie...

Join our Berlin team as a Sales Support Specialist in the dynamic MedTech sector. You will provide crucial commercial and administrative support, coordinating projects and optimizing workflows. The role requires fluency in German, tender management experience, and proficiency in CRM tools like Sa...

Join Proclinical as a fully remote Regulatory Operations Specialist in Europe. You will drive flawless FDA and EMA submissions for oncology and biotech therapies using eCTD software like DocuBridge. Your expertise in preparing INDs, NDAs, and key documents will ensure compliance and advance life-...