Start up Specialist Spain

Business Development Director Business Development Director, EuropeLocation: Flexible across Europe (UK, Germany, Italy, Spain)We are seeking an experienced channel and commercial leader to drive channel growth, aftermarket performance, and strategic business development initiatives across Europe.This is a high-impact leadership role with responsibility for...

Company Description Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a Start up Specialist office based in Spain. Job Overview Responsible

Resourcing Life Science Ltd. is assisting a Global CRO in Spain seeking a Start up Specialist to manage EC/CA submissions and ensure GCP compliance. You will coordinate translations, support phase II-III studies, and work closely with sponsors. Fluent English and Spanish, strong communication, and at least one year in EC/CA submissions are required; this is...

Precision for Medicine is a global Clinical Research Organization with uniquely integrated offering which enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology, in...

Precision Medicine Group is seeking a Regulatory and Start Up Specialist based in Spain (remote) who will drive regulatory submissions and site activation activities for clinical trials. Fluency in Portuguese and English is required, with experience in contracts and budgeting negotiations for Spain. The role collaborates with regulatory leads, start-up...

CTI Clinical Trial and Consulting Services is seeking an experienced Regulatory Affairs professional to support Study Start-Up (RASSU) activities across multiple countries. You will advise project teams on regulatory requirements and oversee submissions to IRBs/ECs, ensuring quality and compliance across sites. Responsibilities include adapting study...

Medicine moves forward here. So willyou. Ergomedis a specialist clinical research organization focused on rarediseaseand select oncology indications. We focus on the most complextrials,the studies where experience, judgement, and rigorous operational accountability make the biggest difference. We partner with small to midsize biotech companies to move...

Ergomed Group is a specialist clinical research organization focused on rare disease and select oncology indications, with global presence and a collaborative culture. The Specialist, Study Start Up and Regulatory Affairs leads and coordinates all activities related to achieving site initiation readiness and regulatory compliance. Role requires a graduate...

Resourcing Life Science Ltd. is assisting a Global CRO in Spain seeking a Start up Specialist to manage EC/CA submissions and ensure GCP compliance. You will coordinate translations, support phase II-III studies, and work closely with sponsors. Fluent English and Spanish, strong communication, and at least one year in EC/CA submissions are required; this...