Senior Clinical Trial Activation Specialist

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...

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...

We are seeking a highly skilled Clinical Nurse Specialist to join our team at ICON Plc. This role is based in Ireland, with opportunities to work from home or the office.About ICON Plc:ICON Plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence.This...

**Job Overview**Iqvia Argentina is seeking a Clinical Trial Support Specialist to join our team. The ideal candidate will have high school or university diploma and clinical research administrative support experience.**Key Responsibilities:**

Role OverviewWe are seeking a Senior Biostatistics Expert to join our EMEA team. This role will involve designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

Job SummaryWe are seeking a highly motivated Clinical Research Associate to join our team in conducting global clinical trials. As a key member of our team, you will be responsible for the successful execution of clinical trials from initiation to closeout.

Senior Clinical Research AssociateWe are seeking an experienced Senior Clinical Research Associate to join our team in Portugal. As a key member of our Clinical Operations group, you will play a crucial role in delivering high-quality clinical trials across commercial and government contracts.About the RoleMonitor investigator sites with a risk-based...

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...

Job SummaryWe are seeking a highly skilled Clinical Trials Specialist - Contract Negotiator to join our team at ICON plc. In this role, you will play a vital part in driving the costings and contracts for clinical trials, responsible for negotiation and budgeting.About UsICON plc is a world-leading healthcare intelligence and clinical research organisation....

OverviewAt Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale.We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies.Salary and BenefitsThe estimated salary for this role is...

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...

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 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 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 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...

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...

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,...

About the RoleAs a Senior Site Activation Professional at ICON, you will be responsible for managing multiple projects and site activation personnel. This role requires exceptional leadership skills, with a collaborative approach to driving performance and success.We are seeking an experienced professional with a proven track record in project management 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...

MAI Fortrea Development Limited is a leading global contract research organization with a passion for scientific rigor and decades of clinical development experience.SalaryWe offer a highly competitive compensation package, including a salary range of $80,000 - $120,000 per year, depending on experience, as well as various local benefits such as pension...