Medical Data Review Specialist II

As a leading global contract research organization (CRO), Fortrea provides pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas.The Medical Data Review Specialist II is a senior member of the Global Medical Data Review Team...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas.The Medical Data Review...

Job Summary: We are seeking a skilled Medical Data Review Specialist II to join our Global Medical Data Review Team. The successful candidate will be responsible for the execution of key Central Medical Review activities and will assist senior staff and Medical Monitors in the execution of their responsibilities.Key Responsibilities:Collaborate with the...

Job Title: Medical Data Review SpecialistJob Summary: We are seeking a highly skilled Medical Data Review Specialist to join our team at MUM Fortrea Development India Pvt Ltd. As a Medical Data Review Specialist, you will be responsible for executing key Central Medical Review activities and assisting senior staff and Medical Monitors in the execution of...

At MUM Fortrea Development India Pvt Ltd, we are seeking a highly skilled Senior Medical Data Review Specialist to join our team of experts in clinical trials. As a senior member of our Global Medical Data Review Team, you will be responsible for executing key Central Medical Review activities and assisting senior staff and Medical Monitors in their...

Job Title: Certifier II - Medical Devices SpecialistAbout the RoleWe are seeking a highly skilled Certifier II - Medical Devices Specialist to join our team at CSA Group. As a key member of our certification team, you will play a crucial role in ensuring that medical devices meet the highest standards of safety and performance.Key ResponsibilitiesProvide...

Position Overview Lilly is seeking a highly skilled Clinical Review Specialist to join our Medical Affairs team. As a Clinical Review Specialist, you will play a critical role in reviewing and approving medical content to ensure it meets the highest standards of accuracy, quality, and regulatory compliance. You will collaborate closely with...

Job Summary:The Associate Medical Data Review Manager is a critical role within IQVIA that requires a strong understanding of clinical data and medical terminology. The successful candidate will serve as a Subject Matter Expert in clinical data sciences, providing medical, clinical, and scientific advisory expertise.Key Responsibilities:Serve as a Subject...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas.The Central Medical Review...

About the Role:Department – Centralised Monitoring Unit (CMU)We are seeking a skilled Senior Medical Reviewer to join our Centralised Monitoring Unit (CMU) team. The successful candidate will be responsible for conducting comprehensive medical reviews of clinical trial data across various therapy areas within our drug development portfolio.Key...

As a leading global contract research organization (CRO), Fortrea is committed to delivering high-quality clinical development solutions to pharmaceutical, biotechnology, and medical device customers. We are seeking a highly skilled Medical Data Review Associate Manager to join our Global Medical Review Team.Key Responsibilities:• Collaborate with...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas.The Associate Medical Data...

Job SummaryWe are seeking a highly skilled and detail-oriented Clinical Data Analyst II to join our team at Parexel. As a Clinical Data Analyst II, you will be responsible for performing clinical data validation activities on assigned projects, ensuring compliance with corporate quality standards, SOPs, ICH-GCP, and international regulatory requirements.Data...

Clinical Data Analyst IIAbout the Role:The Clinical Data Analyst II is a key member of the Clinical Study Team, responsible for performing clinical data validation activities on assigned projects. This role requires strong technical aptitude, attention to detail, and excellent problem-solving skills.Key Responsibilities:Perform data validation activities,...

At MMS Holdings Inc., we are seeking an exceptional Medical Case Reviewer to join our team.We are a leading clinical research organization (CRO) that prides itself on being a Great Place to Work certified organization, recognized for our exceptional culture and industry-best employee retention rate.As a Medical Case Reviewer, you will be responsible...

About the Role:The Central Medical Review Associate is an integral part of our Global Medical Review Team, responsible for the execution of key Central Medical Review activities within the Central Monitoring strategy. This involves collaborating with stakeholders to ensure effective execution of Central Monitoring/Central Medical Review Plans and meeting...

Job Summary:CSA Group is seeking a highly skilled and experienced Product Safety Certifier-II in the Healthcare segment to provide high-quality certification in accordance with medical device product safety standards.This role requires a strong understanding of safety standards for North America, Canada, and IEC, particularly for medical devices and testing...

Quality Assurance for BaxterBaxter is a leading company in the development of medical devices and pharmaceuticals. As a Quality Assurance Specialist II, you will play a crucial role in ensuring the quality of our products and processes.Key Responsibilities:Implement and maintain quality systems to ensure compliance with regulatory requirements.Ensure quality...

The OpportunityWe are seeking a skilled Medical Content Specialist to join our team at Snaphunt. As a Medical Content Specialist, you will be responsible for creating high-quality medical and scientific documents, including clinical study reports, regulatory submissions, journal articles, abstracts, posters, and white papers.Key Responsibilities:Content...

Job Title: Medical, Legal and Regulatory Reviewer (MLR)The Medical, Legal and Regulatory (MLR) review process is a critical component of healthcare marketing, ensuring that advertising, promotional, and non-promotional content is accurate, compliant, and ready for publication. As an MLR Reviewer, you will play a key role in rigorously controlling and...