We believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities that foster an inclusive environment. Instituto Grifols S.A. is seeking a Clinical Scientist for our Clinical Development team. This roles mission is to contribute to developing scientific strategies for new indications, evaluate scientific literature, and interpret data for regulatory documents. It supports MDs with clinical inquiries, ongoing trials, risk evaluation, safety narratives, and Advisory Boards, ensuring smooth regulatory and trial processes. What your responsibilities will be Participate in the design and development of study protocols/protocol amendments, supporting the lead physician in creating overall clinical programs for new therapeutic indications. Collaborate with Biostatistics, Clinical Operations, Pharmacology, and Pharmacovigilance teams to oversee ongoing programs with several clinical studies and to address various indications in development for business considerations. Synthesize literature and competitive intelligence to inform study designs and results within the assigned therapeutic area. Contribute to (and/or review) specific study documents managed or owned by clinical/regulatory groups, such as Investigator Brochures, Pediatric Plans, Briefing Books, Clinical Study Reports, clinical section reviews of BLAs, SAE narrative construction, etc. Support the Regulatory department in preparing for Health Authority meetings (e.g., pre IND meetings, and briefing meeting requests & packages). Support Clinical Operations throughout trial execution, providing an additional layer of quality and expertise to clinical programs through participant data reviews, protocol deviation assessments, and risk evaluations to aid mitigation efforts. Address clinical inquiries from all countries regarding marketed products or new submission dossiers. Help develop strategies to periodically update the clinical sections of core dossiers. Participate in the scientific review process during potential due diligence assessments of external opportunities, presenting and defending conclusions before appropriate committees. Facilitate the compliance and contractual agreement to onboard Key Opinion Leaders (KOLs) and external experts, as well as steering advisory boards, and participate in scientific exchange meetings. Who you are To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Bachelors Degree in Health Sciences or related field. 2+ years of experience as a Clinical Trial Scientist or 5+ years as a Clinical Program Leader (or equivalent). Significant experience in clinical document production and/or clinical trial feasibility and strateg