Regulatory and Start-Up Specialist

Job Title: Regulatory and Start-Up SpecialistLocation: Madrid, SpainJob Type: Regular full-timeDivision: Precision for MedicineBusiness Unit: Clinical SolutionsRequisition Number: 4749Precision Medicine Group is a leading provider of clinical trial services. We are seeking a Regulatory and Start-Up Specialist to join our team in Spain. This position can be...

Regulatory and Start-Up SpecialistAt Precision Medicine Group, LLC., we are seeking a highly skilled Regulatory and Start-Up Specialist to join our team in Spain. This role can be offered fully home-based.Key Responsibilities:Deliver site activation readiness within assigned countries/sites, ensuring timeliness and quality.Prepare and submit Clinical Trial...

Regulatory and Start-Up SpecialistPrecision for Medicine is a leading Contract Research Organization (CRO) that combines innovative technologies, expertise, and operational scale to accelerate the development of life-changing therapies. We are seeking a highly skilled Regulatory and Start-Up Specialist to join our team in Spain. This role can be offered...

At Precision for Medicine, we're pushing the boundaries of what's possible in the life sciences. As a Regulatory and Start-Up Specialist, you'll play a critical role in helping us bring life-changing therapies to patients faster, cheaper, and with greater success. Your expertise will be key in integrating clinical trial execution with deep scientific...

Job OverviewAs a Regulatory and Start Up Specialist 2 at IQVIA, you will be responsible for performing tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements, and contractual/budgetary guidelines.Key...

Job DescriptionThe Study Start Up and Regulatory Specialist is a key member of our team, responsible for ensuring the successful initiation and execution of clinical trials. This involves collaborating with internal stakeholders, authorities, vendors, and investigative sites to plan, organize, and execute study start-up and regulatory deliverables.Key...

Study Start-Up Associate RoleThis challenging role involves leading the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.Key Responsibilities:Leading the preparation and submission of regulatory documents, including clinical trial applications, ethics...

Job Summary:As a Clinical Research Associate - Site Start-Up Specialist at Boston Scientific, you will play a critical role in supporting the Global Clinical Operations Center of Excellence. Your primary responsibility will be to conduct site start-up activities for clinical trials, ensuring compliance with regulatory requirements and company policies. This...

Job DescriptionPrecision for Medicine is a cutting-edge CRO that integrates clinical trial execution with scientific knowledge, laboratory expertise, and advanced data sciences. As we continue to grow, we are seeking a Regulatory and Start-Up Specialist to join our team in Spain. This position offers the opportunity to work fully from home. Key...

Regulatory and Start-Up Specialist OpportunityPrecision for Medicine is a pioneer in clinical trial execution, combining cutting-edge technologies, expertise, and operational scale to accelerate the development of life-changing therapies. We're seeking a skilled Regulatory and Start-Up Specialist to join our team in Spain, working closely with our...

About the RoleThe Clinical Research Associate (CRA) supports the Global Clinical Operations (GCO) Centre of Excellence, conducting activities consistent with GCO's mission of building a world-class shared clinical technology, process innovation and clinical operations team, in partnership with the company's divisions, through technology enablement,...

About the RoleThe Clinical Research Associate (CRA) supports the Global Clinical Operations (GCO) Centre of Excellence, conducting activities consistent with GCO's mission of building a world-class shared clinical technology, process innovation, and clinical operations team, in partnership with the company's divisions, through technology enablement,...

About Precision for MedicinePrecision for Medicine is a leading Contract Research Organization (CRO) dedicated to delivering high-quality services to the pharmaceutical and biotech industries.Job SummaryWe are seeking an experienced Start Up Lead/Senior Start Up Lead who has a passion for site start-up to join our team. The ideal candidate will work remotely...

About the RoleThe Clinical Research Associate supports the Global Clinical Operations Centre of Excellence, conducting activities consistent with GCO's mission of building a world-class shared clinical technology, process innovation, and clinical operations team, in partnership with the company's divisions, through technology enablement, high-touch customer...

Job OverviewErgomed Group is a rapidly expanding full-service CRO specializing in Oncology and Rare Disease. Our company offers employee visibility, creative contribution, and realistic career development in an international culture that values employee experience, well-being, and mental health.About the RoleWe are seeking a highly skilled Global Regulatory...

About RevolutAt Revolut, we believe that everyone deserves more from their money. That's why we're on a mission to deliver a financial super app that's faster, cheaper, and more secure than traditional banks. Our team is made up of brilliant people who love building great products, redefining success, and turning complexity into simplicity.About the RoleThe...

About the Role: Precision Medicine Group is seeking a skilled Site Start-up Expert to oversee the site start-up process and ensure timely delivery of site start-up activities.Key Responsibilities: Develop and implement an activation readiness strategy, coordinate critical path planning, and collaborate with stakeholders to secure input for milestone...

SIX Group Services Ltd. is at the forefront of transforming financial markets in Europe.Role OverviewWe are looking for a highly skilled Regulatory Framework Specialist to join our team in Madrid. As a Regulatory Framework Specialist, you will play a pivotal role in monitoring regulatory developments and ensuring compliance for SIX Clearing across the EU,...

OverviewIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. Our mission is to push the boundaries of human science and data science to make a significant impact in creating a healthier world.About the RoleWe are seeking an experienced Regulatory Start-up/Site Activation...

Regulatory Affairs Specialist Role:We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Ventós Group in Sant Just Desvern, Barcelona. As a Regulatory Affairs Specialist, you will play a key role in maintaining our product database, collaborating with suppliers to homologate new products, preparing technical documentation, and...