Responsibilities: Provide scientific and technical expertise for CMC activities supporting a commercial biotech product. Collaborate with CMOs to manage manufacturing, ensuring quality, compliance, and timely delivery. Develop and execute CMC strategies aligned with company goals and regulatory standards. Review and approve batch records, analytical data, and technical reports. Contribute to re...
Read moreJob Title: Freelance Clinical Research Associate (CRA) – Oncology Location: Florida, United States (Remote with Regional Travel) Contract Type: Independent Contractor / Freelance FTE: 0.7 Therapeutic Area: Oncology Start Date: Immediate Travel Requirement: Approximately 50–60% within Florida Position Overview We are currently seeking an experienced and highly motivated Freelance Clinical Resear...
Read moreJob Opportunity: DeltaV Engineer (DeltaV Live & DeltaV Batch Experience Required) Are you an experienced DeltaV Engineer looking for an exciting new challenge? Our client, a leading consultancy working with top-tier companies in the pharmaceutical and life sciences sector, is seeking a skilled professional to join their team. This is a fantastic opportunity to contribute to high-impact proj...
Read moreAre you an experienced DeltaV Project Manager looking for your next exciting opportunity? We are working with a leading consultancy that partners with top-tier clients in the pharmaceutical and biotech industries to deliver cutting-edge automation solutions. This is a contract opportunity with the potential for long-term collaboration, offering exposure to high-profile projects and the chance t...
Read moreSenior Manager, QMS & GMP Global Quality Assurance Our client are seeking a (Senior) Manager, GMP QA to join its dynamic Quality Assurance team. This role is essential for maintaining and improving the company’s Quality Management System (QMS) and ensuring compliance with Good Manufacturing Practice (GMP) standards. Key Responsibilities Enhance and implement the company’s QMS to […]
Read moreQualified Person for Pharmacovigilance Permanent, Hybrid Location: Netherlands Driven by their mission to transform the lives of patients with rare, life-threatening diseases, this biopharma develop and commercialise innovative protein replacement therapies and precision medicines. Reporting to the VP of Global Pharmacovigilance, as QPPV, you will play a critical role in ensuring patient safety...
Read moreAre you an experienced Clinical Study Nurse with a passion for advancing medical research? Do you thrive in dynamic environments and excel at supporting clinical trials? We are looking for a highly skilled and motivated Freelance Clinical Study Nurse to join our team on an as-needed basis. Key Responsibilities: Collaborate with investigators and site staff to ensure […]
Read morePosition: Scientific Strategy Program Lead An innovative pharmatech company is looking for a strategy driven program lead to assist with the development of their drug discovery programs. The role involves advising members across multidisciplinary teams influencing the technological developments within the pipeline. Key Responsibilities: Define program milestones and develop new programs Impleme...
Read moreJob Title: Senior Medical Director, Ophthalmology A leading pharmaceutical company is seeking a dynamic and imaginative physician drug developer to lead the clinical development of innovative therapeutics. The role involves driving clinical strategies, overseeing trials, collaborating across teams to ensure integrated product development and leading a team. Key Responsibilities: Provide strateg...
Read moreScienta are proud to be partnered with a leading Pharmaceutical company Head Quartered in the NRW area, on the search for a new QA Manager to join their teams. Overview: Ensure that assigned contract manufacturers, comply with EU-GMPs, international guidelines and internal quality standards. Support in analytical method transfer projects to new laboratories. Qualifications and […]
Read moreAct as the main point of contact for investigators, monitors, study centres, authorities, sponsors, and patients. Take care of study patients, including scheduling appointments according to the protocol. Handle the organization and coordination of diagnostics, lab work, sample shipments, and study medications. Collect, record, and manage all study data while setting up appointments as per [&hel...
Read moreHead of Clinical Operations This role is open to candidates at Senior Director or Executive Director level. Location: Boston MA / and neighbouring states (required to be in the office once every few weeks) About the Company A dynamic and innovative pharmaceutical company, specializing in oncology-focused therapeutics, is seeking an accomplished leader to join its team. […]
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