The Associate Director, Clinical QA will provide Quality oversight for the end-to-end clinical process for the clinical trials under responsibility to ensure compliance with the Health Authorities requirements, the internal standards and a full adherence to patients' safety, rights and well-being. P...
Therapy Associates is hiring Clinical Fellows who are seeking placement to complete their required hours to receive their permanent license! We have experienced and dedicated supervisors on staff!. Therapy Associates takes pride in the relationships we have with our providers! Our admin staff is ava...
Clinical Research, Clinical Study Reports, Clinical Trial Management Systems (CTMS), Clinical Trials, Clinical Trials Monitoring, Communication, Data Integrity, Decision Making, Life Science. Proactively collaborates with the Clinical Project Manager (CPM) and CRA Manager as well as Medical Scientif...
Associate II, Vendor Outsourcing. Associate II, Vendor Outsourcing. Associate II, Vendor Outsourcing. This role responsibilities include: facilitating vendor selection, RFI, RFP, contracting, and negotiation with a focus on CRO services outsourced in support of clinical trials. ...
Budget Management, Clinical Research, Clinical Trial Protocol, Clinical Trials, Coaching, Cross-Functional Teams, Data Analysis, Learning Design, Lifesciences, Risk Management, Risk Monitoring. The Associate Director CD DEI CoE will support the Head, CD DEI CoE in defining and implementing the Novar...
The Senior Clinical Research Associate (CRA) will act as a liaison between Ferring (the study Sponsor) and the sites/clinics that conduct their assigned clinical studies. Ensure site(s) maintains an acceptable inventory of clinical supplies and associated documentation. Focused primarily on ensuring...
Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. Good knowledge of, and skill in applying, ...
Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. Good knowledge of, and skill in applying, ...
Must be licensed as a Licensed Clinical Psychologist, Licensed Marriage and Family Therapist (LMFT), Licensed Clinical Social Worker (LCSW) or Licensed Professional Counselor (LPC). We’ll help you craft a provider profile that highlights your specialities and clinical approach, making it easier for ...
Clinical Study Associate Manager Hematology/Oncology. The successful candidate will be supporting the clinical study lead on multiple phase 2/3 hematology/oncology trials. ...
Must be licensed as a Licensed Clinical Psychologist, Licensed Marriage and Family Therapist (LMFT), Licensed Clinical Social Worker (LCSW) or Licensed Professional Counselor (LPC). We’ll help you craft a provider profile that highlights your specialities and clinical approach, making it easier for ...
The Clinical Trial Capabilities (CTC) organization offers infrastructure, support, and solutions enabling the Clinical Operations and Development Organizations with rapid, efficient, and compliant clinical trial execution to deliver transformative medicines to patients. The Associate Director, will ...
Senior Clinical Research Associate. 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. ...
Under the direction of the Director, Study Management, the Clinical Trial Associate (CTA) Study Management, will be responsible for supporting the Global Clinical Trial Operations department, Study Directors and Study Managers in the conduct and oversight of the execution of Phase - studies, as well...
Job Description Summary: The Senior Specialist, Clinical Trial Associate provides clinical study and Trial Master File (TMF) support for clinical operations. The Senior Specialist, Clinical Trial Associate supports adherence to relevant regulatory requirements and company Standard Operating Procedur...
The Center for Social Justice (CSJ) has an opening for an Assistant or Associate Clinical Professor to teach the Family Law Clinic. The Assistant/Associate Clinical Professor will teach the Family Law Clinic. The Assistant/Associate Clinical Professor will teach the weekly two-hour seminar for the F...
Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. IQVIA is a leading global provider of adva...
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. ...
The Senior Clinical Research Associate (CRA) will act as a liaison between Ferring (the study Sponsor) and the sites/clinics that conduct their assigned clinical studies. Ensure site(s) maintains an acceptable inventory of clinical supplies and associated documentation. Focused primarily on ensuring...
Therapy Associates is hiring Clinical Fellows who are seeking placement to complete their required hours to receive their permanent license! We have experienced and dedicated supervisors on staff!. Therapy Associates takes pride in the relationships we have with our providers! Our ad...
Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. As a Sr CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Have a mini...
Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice. If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices accordi...
Primary responsibilities of a faculty member at the clinical site will include educating Fairleigh Dickinson University students, residents (if applicable), and pharmacy staff, providing and documenting pharmacotherapeutic interventions/pharmacy consultations, attending interdisciplinary rounds (whe...
We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development as a Clinical Research Associate II. ICON plc is a world-leading healthcare intelligence and clinical research organization. Cond...
Works with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to manage site trends through dashboard review and ongoing risk assessment to ensure quality standards and address concerns associated with study delivery at sites within established protocols and portfolio under gene...