Regulatory Manager, Clinical Trials Regulatory Expert

About the RoleWe are seeking a Clinical Trial Regulatory Affairs Specialist to join our global Regulatory Affairs department – Regulatory Science team. This is a fantastic opportunity to further develop your regulatory career and expertise in a global clinical trial setting.Job DescriptionIn this role, you will be a pivotal team member with regulatory...

Thermo Fisher Scientific, a leading global biotechnology company, is seeking an experienced Regulatory Affairs Specialist to join our Global Clinical Trial team. With a competitive salary of $120,000 per annum, this role offers a unique opportunity to contribute to the development and implementation of regulatory strategies for clinical trials...

Job OverviewWe are seeking a highly skilled Clinical Trials Project Manager to lead our site management efforts in the development of life-changing therapies.As a Clinical Trials Project Manager, you will be responsible for overseeing the implementation of clinical trial projects from initiation to close-out. Your expertise will be crucial in ensuring...

Embark on a challenging career opportunity as a Regulatory Affairs Specialist at Icon Plc, a leading healthcare intelligence and clinical research organization.We are seeking an experienced individual to lead the preparation and submission of regulatory documents, including clinical trial applications, ethics committee submissions, and regulatory agency...

Unlock your potential as a Senior Clinical Study Manager at Mygwork - LGBTQ+ Business Community, where diversity and inclusion thrive. We are seeking an experienced professional to lead clinical trials with moderate complexity, providing quality oversight and driving decision-making.Job SummaryAs a Senior Clinical Study Manager, you will be responsible for...

About Us: Fortrea is a leading global contract research organization (CRO) dedicated to revolutionizing the development process for pharmaceutical, biotechnology, and medical device customers. With decades of clinical development experience and a passion for scientific rigor, we provide a wide range of clinical development, patient access, and technology...

Job SummaryWe are seeking a highly motivated and experienced Clinical Trials Project Manager to join our team at Fortrea. The successful candidate will be responsible for site monitoring, site management, and ensuring the integrity of clinical trials.Responsibilities:Responsible for all aspects of study site monitoring, including routine monitoring and...

About the RoleClinical Trial Administrators at Iqvia Argentina play a vital role in ensuring the success of our clinical trials. As a Sr Clinical Trial Assistant/Start-Up, you will be responsible for coordinating and administering daily administrative activities to ensure a complete and accurate Trial Master File delivery.Key Responsibilities:Assist Clinical...

ICON plc is a world-leading healthcare intelligence and clinical research organization. Our mission is to shape the future of clinical development.We're looking for a Senior Clinical Trial Operations Manager to join our team in EMEA. As a key member of our team, you will be responsible for advancing clinical trial start-up activities by understanding client...

Job Summary">We are seeking a highly motivated Senior Clinical Research Associate II to join our global clinical trial management team. As a key member of the team, you will be responsible for site monitoring and site management for clinical studies according to Fortrea Standard Operating Procedures and Regulatory Guidelines.">About the Role">The Senior...

OverviewFortrea, a leading global contract research organization, offers a unique opportunity for a skilled Clinical Trials Project Manager to join our team. With a passion for scientific rigor and decades of clinical development experience, we provide pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development,...

TFS HealthScience is a leading global Contract Research Organization (CRO) partnering with biotechnology and pharmaceutical companies throughout their clinical development journey. We provide full-service capabilities, resourcing, and Functional Service Provider (FSP) solutions, helping bring life-saving treatments to patients worldwide.Sponsor: You will be...

About Noesis PortugalNoesis Portugal is a leading organization in the industry, continuously investing in training and development of its talented professionals. We are seeking a highly skilled Regulatory Projects Manager to join our team.Job Summary:We are looking for a Regulatory Projects Manager with a strong background in project management and...

Company OverviewMai Fortrea Development Limited is a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience. We provide pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20...

Role OverviewWe are seeking a seasoned Regulatory Projects Manager to lead the implementation of regulatory changes and oversee COREP/Pillar 3 reporting projects for our organization.About the RoleThis is a challenging opportunity to utilize your expertise in project management, risk analysis, and regulatory compliance to drive operational excellence within...

About the RoleWe are seeking an experienced Strategic Regulatory Projects Manager to lead our team in Lisbon. This is a challenging role that requires strong regulatory, prudential, and accounting skills.Key ResponsibilitiesManage HR topics such as recruitment, target setting, appraisals, and coach new joiners.Develop good working relationships with...

Regulatory Projects Team Leader Job DescriptionFórum Selecção is a prominent player in the recruitment industry, and as such, we are looking for a highly skilled Regulatory Projects Team Leader to join our Corporate Client team in Lisboa. The successful candidate will be responsible for managing a team of Project Managers and ensuring the efficient...

About Iqvia LlcIqvia Llc is the Human Data Science Company oriented to drive human health outcomes forward.As a sponsor-dedicated Senior Clinical Research Associate, you'll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers.You will be responsible for:Performing site...

Job OverviewThe Associate Principal Scientist, Regulatory Affairs, Chemistry Manufacturing and Controls position at Organon is a key role in facilitating and implementing global regulatory strategies for small molecule products. This expert will work closely with the CMC Product Lead to ensure the successful execution of project...

Unlock Your Potential as a Regulatory Excellence Manager with Sanofi Consumer Healthcare!About the RoleWe are seeking an exceptional Regulatory Excellence Manager to join our team in Neuilly-sur-Seine, France / Barcelona, Spain / Lisbon, Portugal / Athens, Greece / Bucharest, Romania. As a key member of our Regulatory Excellence team, you will play a...