Clinical Trials Compliance Specialist

We are seeking an experienced Clinical Trial Operations Specialist to join our team. As a Clinical Trial Operations Specialist, you will be responsible for the local management of clinical trials in countries around the world.This role is the primary point of contact at a country level for assigned studies and has operational oversight of assigned...

Delivering high-quality clinical trials requires a dedicated and skilled professional. As a Clinical Operations Specialist I, you will play a vital role in supporting the successful execution of these trials.

Clinical Trial Manager JobWe are seeking a highly skilled Clinical Trial Manager to join our team. This is an exciting opportunity for someone who wants to be part of a dynamic and fast-paced environment.This role will involve managing clinical trials from start-up through to database lock and closeout activities. The successful candidate will be responsible...

Clinical Trials Development SpecialistMilestone One supports global clinical study sites to achieve stronger study delivery.Key responsibilities include:Building and maintaining relationships with key stakeholdersIdentifying and capitalizing on business opportunitiesRequirements for success:Proven track record in business development or a related...

Clinical Trials Legal and Compliance Manager**Category**:Legal, Compliance & Audit**Location**:São Paulo, São Paulo, BR**The Position**- As a Clinical Trials Legal and Compliance Manager at Novo Nordisk, you will be responsible for overseeing all legal and compliance matters related to clinical trials in Brazil, ensuring adherence to laws, internal...

Clinical Research Associate Role OverviewThe Clinical Research Associate plays a pivotal role in ensuring the integrity and quality of clinical trials. As a primary CRA, you will conduct site visits, manage relationships with key site personnel, and monitor data quality to ensure patient safety and compliance with regulatory guidelines.

Medical ConsultantWe are seeking a highly skilled medical consultant to join our team. The ideal candidate will possess a strong background in clinical trials, with experience working in contract research organizations, pharmaceutical companies, or as a principal investigator.Key Responsibilities:Provide medical oversight of clinical trials to ensure...

Job Title: Clinical Trials Specialist">This role is responsible for managing the contract process for clinical trials, including negotiating and preparing contracts, budgets, and related documents.The successful candidate will have experience in a contract research organization or pharmaceutical industry and possess strong knowledge of the clinical...

Site Monitoring SpecialistThis role involves conducting on-site monitoring activities at investigator sites to ensure compliance with clinical trial protocols and regulatory requirements. The successful candidate will apply a risk-based monitoring approach, utilizing root cause analysis (RCA) and critical thinking skills to identify site processes failures...

Objective:We are seeking a highly skilled Senior Clinical Research Associate II to support our clinical development activities. This key role involves conducting site visits and monitoring clinical research studies to ensure compliance with industry standards and regulations.">Key Responsibilities:Conduct on-site and remote monitoring of clinical research...