Our clinical operations activities are growing rapidly and we are currently seeking full-time, Regulatory Submissions Technical Advisors to join our Site Activation and Maintenance team, within Clinical Operations.This role will be office-based in Madrid.This position plays a key role at Medpace, p reparing and reviewing regulatory documents and providing strategic regulatory advice to support clinical trial submissions .Medpace specialises in supporting mid-sized biopharma companies giving you the opportunity to work on complex and challenging trials, often involving new technologies and novel therapies.If you want an exciting role where you use your previous expertise and can develop and grow your career even further,then this is the opportunity for you.Responsibilities- Provide regulatory submissions strategic advice and guidance to the Regulatory Submissions Manager (RSM), Medpace project team and Sponsor to ensure submissions compliance with appropriate regulations and requirements;- Prepare and / or review core trial documents for compliance with relevant guidelines / regulations and for trial suitability;- Prepare and maintain Part I EU CTR submissions- Review pertinent regulations and guidance to develop proactive solutions to regulatory issues and challenges;- Independently interact with Sponsors, regulatory agencies and Medpace colleagues; and- Present during bid defences, general capabilities meetings and audits, as required.Qualifications- Bachelor's degree in Life Sciences - Master's / PhD preferred;- Significant experience in regional / global regulatory submissions;- Strong understanding of regulatory documentation, guidelines and legislation;- Ability to review regulatory guidance and develop proactive solutions to regulatory issues and challenges;- Experience in reviewing and / or writing core regulatory documents;- Strong communication, critical thinking and problem-solving skills;- Ability to independently interact with national / regional regulatory agencies.Medpace OverviewMedpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries.Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach.We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.Headquartered in Cincinnati, Ohio,employing more than 5,000 people across 40+ countries.Why Medpace?People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas.The work we do today will improve the lives of people living with illness and disease in the future.Medpace Perks- Hybrid work-from-home options (dependent upon position and level)- Competitive PTO packages- Company-sponsored employee appreciation events- Employee health and wellness initiatives- Flexible work schedule- Competitive compensation and benefits package- Structured career paths with opportunities for professional growthAwards- Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibilityWhat to Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.EO / AA Employer M / F / Disability / VetsHace 2 díasEscribe tu dirección de correo electrónico, te permitirá de estar al tanto de los últimos empleos por: (sdj646) | regulatory submissions technical advisor (regulatory affairs, study start-up) Escribe tu dirección de correo electrónico, te permitirá de estar al tanto de los últimos empleos por: (sdj646) | regulatory submissions technical advisor (regulatory affairs, study start-up)#J-18808-Ljbffr
