Clinical Trial Coord

We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD part of TFS — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering...

**Description** **Clinical Trial Manager any therapeutic area-Home based LATAM** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and...

**Qualifications**: Education and Experience: High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification. Bachelor's degree preferred. Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 1 year). In some cases, an equivalency, consisting of a combination...

CTA - Clinical Trial Assistant page is loaded CTA - Clinical Trial Assistant Apply locations Mexico City, Mexico time type Full time posted on Posted 3 Days Ago job requisition id R1425119 Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and...

Provides administrative and technical support to the Project Team. Supports audit readiness by ensuring files are reviewed on schedule detailed in the organization's WPD and department guidance document. Essential Functions: - According to the specific role (Central or Local), coordinates, oversees and completes functions on assigned trials activities...

Job DescriptionThis position plays a key role in overseeing trial and site administration. Working closely with senior management, the individual is responsible for preparing, organizing, distributing, and archiving clinical documents. In addition, they provide vital support for clinical and non-clinical supply management, ensuring accurate tracking and...

Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...

Job DescriptionThis role is responsible for comprehensive trial and site administration. Under the oversight of the Senior COM or COMs or CTC Manager, the person prepares, collates, distributes and archives clinical documents.The CTC supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as...

**CTC-L** We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering...

IQVIA Biotech is committed and dedicated to the small biotech & biopharma companies we support. Opportunities available for an experienced Clinical Trial Manager II or Senior Clinical Trial Manager. Previous clinical trial management and CRO experience preferred. Therapeutic requirements/preference: any of the following Oncology/Hematology/CAR T/Cell &...

Oversees daily operational excellence for area of responsibility and/or assigned projects. Mentors and supports Associate Directors, Directors and other members of their project teams. Collaborates cross functionally with other departments to meet overall business objectives and provide strategic input to new services. Provides global strategic direction,...

**About the role**: Curebase is seeking a Clinical Quality Associate I who will thrive in a quickly scaling healthcare technology environment. Quality at Curebase is deeply cross-functional, and you will work with nearly every function at the company to conduct risk-based quality management (RBQM) surveillance of Clinical Operations activities at Curebase....

The primary purpose and objective of the Contract Coordinator position is to work with and assist the Contract Analysts in the completion and execution of contracts with clinical study sites and principal investigators ("Clinical Trial Agreements"). **The primary duties of the Contract Coordinator include**: (i) preparation and monitoring of Clinical Trial...

**Description** **SSU & Regulatory Specialist with experience in clinical trials-Client Based Mexico (CDMX)** Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market...

Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on...

Beitrag mit entsprechender Aufsicht zu allen Aspekten globaler klinischer Studien,s), um Studienergebnisse innerhalb von Zeitplan-, Budget-, Qualitäts-/Compliance- und Leistungsstandards zu liefern. Kann bestimmte Aspekte globaler klinischer Studien leiten. Kernmitglied des Clinical Trial Teams, trägt durch Prozessverbesserung und Wissensaustausch zur...

Operations Associate, Clinical Assessment Technologies - Mexico - Remote based Requisition Number 7914 Employment Type : Regular Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new...

Job Overview In-depth knowledge of applicable global, regional and local clinical research regulatory requirement; i.e. Good Clinical Practice (GCP) and International. Provide departmental support to Clinical Event Validation and Adjudication (CEVA) Management and project support to CEVA Project Managers/Leads. Support provided is typically broad in scope...

The SSO Clinical Project Manager (CPM) is accountable for the day-to-day planning, executing and reporting, (from first site initiation visit to and including study site close-out), of assigned Global Drug Development (GDD) studies in compliance with Novartis processes and regulatory requirements. The CPM is the single point of contact and study team lead,...

Job DescriptionThis position is responsible for ensuring performance and compliance for assigned protocols in a specific country, adhering to ICH/GCP and country regulations, company policies, quality standards, and adverse event reporting requirements both internally and externally. Under the guidance of the Head COMs, the individual will oversee the...