SciPro are exclusively partnered with a global rare disease company, supporting their search for an experienced Medical Affairs Manager to join their small, collaborative team in Portugal. The role will be responsible for medical affairs across the whole of the country, and build strong relationships with healthcare professionals, support scientific exchange, and drive medical projects within the territory.  Key Responsibilities Communicate scientific and product knowledge clearly to support business objectives.Develop and maintain relationships with key opinion leaders and clinical investigators.Provide medical training and resources to commercial teams. Requirements 2–3 years’ experience in pharmaceuticals and/or clinical research (rare disease experience beneficial).Strong ability to translate complex scientific information into clear messages.Excellent communication, networking, organisational and interpersonal skills.Able to work independently in a dynamic environment.Willing to travel up to 60%.

  Fachreferent / Pharmareferent (m/w/d) – Innovative Therapien |3 Regionen: Südost (Niederbayern/Oberbayern Ost) · Südwest (Bayern West/BW Süd) · Nord-Südwest (Franken/Nordbaden/Stuttgart–Nürnberg) Das Unternehmen ist der deutsche Ableger eines international operierenden Pharmaunternehmens mit europäischem Hintergrund. Es entwickelt, produziert und vertreibt verschreibungspflichtige Arzneimittel und verfügt über ein breites Portfolio in mehreren europäischen Märkten.Schwerpunkte liegen in der Entwicklung innovativer Arzneiformen und kontrollierter Wirkstofffreisetzung zur Verbesserung der Therapietreue und Patientenversorgung.  Was sind Ihre Aufgaben als "Pharmareferent  (m/w/x)"?   Betreuung von Fachärzten in Kliniken und Praxen – persönlich und über digitale Kanäle.Umsetzung eines integrierten Gebiets- und Kundenplans zur erfolgreichen Positionierung der Marke.Erreichung vereinbarter Umsatz- und Strategieziele.Durchführung lokaler Marktanalysen (quantitativ/qualitativ) und Anpassung der Gebietsplanung.Aufbau und Pflege langfristiger, vertrauensvoller Kundenbeziehungen durch fachliche Expertise und nutzwertorientierte Kommunikation.Identifikation von Bedarf an wissenschaftlichen Projekten bzw. Fortbildungen und Planung/Umsetzung lokaler Aktivitäten.Initiierung und Durchführung lokaler Projekte und Veranstaltungen in Abstimmung mit internen Stakeholdern.Regelmäßiger Austausch zu Best Practices mit internen Kollegen und PartnernEnge funktionsübergreifende Zusammenarbeit mit Medizin, Marketing, Market Access und weiteren internen Bereichen.Sicherstellung der Einhaltung aller relevanten gesetzlichen und compliance-relevanten Vorgaben.  Welche Voraussetzungen benötigen Sie für die Position des"Pharmareferenten (m/w/x)"?  Sachkenntnis gemäß §75 AMG (deutschlandweit anerkannt)Ein naturwissenschaftlicher, pharmazeutischer oder medizinischer Hintergrund ist vorteilhaftErste Erfahrung (mind. 1-2 Jahre) im pharmazeutischen Außendienst mit Rx-ProduktenGrundlegendes Verständnis der Strukturen des deutschen Gesundheitswesens (z. B. Erstattung, Zugang)Nachweisbare Erfolge in der Zielerreichung im AußendienstSicherer Umgang mit Expertinnen aus Klinik und PraxisAusgezeichnete mündliche und schriftliche KommunikationsfähigkeitenFähigkeit zum eigenverantwortlichen Arbeiten und zur GebietsgestaltungGute PräsentationsfähigkeitenSehr gute Deutschkenntnisse in Wort und SchriftSicherer Umgang mit Standard-Office-AnwendungenStrategische und lösungsorientierte DenkweiseHohes Maß an Motivation, Engagement und KundenorientierungTeamplayer mit kooperativer Arbeitsweise   Interesse? „Ich freue mich auf Ihre Bewerbung und ein persönliches Gespräch mit Ihnen. Kontakt für die Bewerbung:  - E-Mail: p.roussos@sciproglobal.de  - Telefon: +49 (0)89 / 21 093938  

SciPro is partnered with a consulting firm seeking a Principal, Market Access to lead and expand its market access practice, partnering with pharmaceutical and biotech clients from Phase II through launch to shape payer strategy, readiness planning, and value communication. This leader will refine service offerings, oversee client deliverables, and drive business development by leveraging strong client relationships and deep knowledge of the payer and pricing landscape. The role requires the ability to synthesize insights into clear, actionable recommendations while managing and mentoring teams to execute high-quality deliverables that support launch and in-line product success. Travel up to 25% may be required. Responsibilities: Refine and expand market access service offerings. Lead client engagements on payer strategy, pricing, and access insights. Synthesize findings into clear, actionable recommendations. Manage and mentor teams to ensure high-quality deliverables. Drive business development with existing and new clients. Monitor market trends to inform client strategy and competitive positioning. Requirements: Bachelor’s in life sciences (MBA preferred). 10+ years in pharmaceutical market access, including 5+ in consulting. Proven track record in delivering results and driving business growth. Deep understanding of payer, pricing, and access strategy. Strong communication, leadership, and client management skills. Willingness to travel up to 25%.

Director, Real World Evidence United States – Remote We're currently partnered with a biotech company seeking a Director of Real World Evidence to lead RWE strategy across development and commercialization. This role will shape how data is used to support clinical development, regulatory submissions, market access, and ongoing product adoption. Key Responsibilities: Develop and drive RWE strategy for pipeline and marketed products. Design and oversee studies using diverse data sources (claims, EMR, registries). Generate evidence to support regulatory, payer, and HTA needs. Partner cross-functionally and with external stakeholders to ensure evidence informs access and clinical practice. Lead dissemination of findings through publications and conferences. Qualifications: Advanced degree (PhD, MD, PharmD, or Master’s) with 10+ years of relevant experience. Background in biotech or pharma; rare disease experience preferred. Strong expertise in observational research, study design, and global RWE/HTA requirements. Proven communication, leadership, and project management skills.

This innovative, late-phase biotech is seeking a Vice President, Head of Quality to define and lead all quality functions across the organization. This role will ensure compliance and operational excellence from early development through commercialization, supporting the company’s mission to bring advanced biologic therapies to patients globally. In this role, you will report to the C-Suite and play a pivotal role in quality strategy, regulatory readiness, and team leadership, overseeing all quality functions. Qualifications: Advanced scientific degree (Master’s accepted, PhD preferred) in a relevant life sciences discipline.Extensive experience (15+ years) in Quality Assurance within pharmaceutical or biotech organizations, with at least 8 years in executive leadership roles.Expertise in biologics development, including large molecule therapeutics and sterile manufacturing.Proven record of guiding products through late-stage development and market launch.In-depth knowledge of global regulatory standards, including FDA, EMA, and ICH, across GMP, GLP, GCP, and GDP.Experience managing and evaluating the performance of external partners such as CDMOs, CROs, and suppliers.Strong history of designing, implementing, and scaling Quality Systems to support organizational growth.  Key Responsibilities: Develop and implement a comprehensive quality strategy aligned with company goals.Build, mentor, and lead a high-performing Quality team, fostering accountability and professional growth.Create and maintain flexible Quality processes suitable for all stages of product development, from pre-IND through commercialization.Oversee global third-party partners to ensure adherence to quality standards and contractual obligations.Lead preparation for regulatory inspections and submissions, proactively addressing issues and mitigating risk.Collaborate with cross-functional teams to integrate quality considerations into operational and strategic decisions.Manage financial and resource planning for the Quality function, optimizing efficiency and impact.  This is a fully remote role with approximately 20% travel, including international travel and occasional evening meetings to coordinate with global teams. There is a strong preference towards candidates on Pacific time.