Clinical Research Associate Ii

**Company Description**PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.As a Clinical Research Associate at PSI you will enjoy a...

Job Title: Clinical Research CoordinatorWe are seeking a highly skilled and detail-oriented Clinical Research Coordinator to join our team. The successful candidate will contribute to the success of our clinical trials by performing independent monitoring activities, ensuring patient safety and data integrity.The ideal candidate will have an undergraduate...

Job Title:Clinical Research Assistant IKey Responsibilities:Provide operational support to the core study team for assigned studies from start-up to closeout and submission.Manage and oversee shared spaces, TMF, and study management platforms.Ensure compliance with regulatory requirements and follow up on information tracking.Required...

Job OpportunityWe are seeking a Clinical Research Manager to oversee the planning, execution and successful completion of clinical trials. This critical role requires ensuring adherence to timelines, budgets, and regulatory guidelines.Key Responsibilities:Plan and manage all aspects of clinical trials, ensuring quality standards.Collaborate with...

Study Manager OpportunityKey to delivering high-quality clinical research programs is our Study Managers.The ideal candidate will provide strategic guidance and oversight to site management team members throughout the study lifecycle. They will serve as the primary point of contact for clinical monitoring and site activities within the project.Provide...

As a Regulatory Affairs Associate at Parexel Consulting, you will support clinical trial submissions to regulatory authorities, focusing on projects in Brazil. This role offers an opportunity to develop skills in regulatory affairs and clinical research while working with experienced professionals. **Key Responsibilities**: - Contribute to high-quality...

Job Overview: As a highly skilled Regulatory Specialist, you will be responsible for maintaining awareness of regulatory legislation, guidance, and practice in assigned countries. You will coordinate, collect and organize data and information required by regulatory authorities, including the preparation of study documentation such as country application...

OverviewClinical Trial Psych Rater - Portuguese Speaking role at IQVIA. Remote/virtual location with approximately 10-16 hours per month. Role: Clinical Specialist with focus on ensuring standardized administration and reliability of assessments in clinical trials.ResponsibilitiesParticipate in all orientation, training and calibration activities as...

Clinical Specialist Consultant -PortugueseSpeakingLocation: Remote/virtualHours: Estimated 10-16h/monthRole: Clinical SpecialistJob Description:The Clinical Specialist reviews scales administered by raters in a clinical trial to ensure that assessments are being conducted in a standardized manner to ensure data reliability. The quality of assessments is...

A Clinical Research Associate is a professional who contributes to accelerated drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity. You will be joining a program takes an extensive co-monitoring approach that enables a supportive and collaborative work environment. Frequent, consistent...