Creative Template Designer for Case Studies and Audit

+ Peer-review style audit for medical study research project · + Conduct comprehensive pre-submission peer-review audit · + Assess methodology and identify potential desk-reject risks. · + Ensure high-quality standards and successful submission of manuscriptes review. · Mandator ...

Lead/manage Good Clinical Practice (GCP) audits, including clinical investigative site audits, clinical vendor audits, · Clinical Study Reports (CSRs) · ...

This position is responsible for providing QA oversight and auditing of activities related to clinical and preclinical studies. · ...

This position is responsible for providing QA oversight and auditing of activities related to clinical and preclinical studies. · Assess and assure study, project, and process compliance with protocols, controlled documents, and applicable regulations. · ...

This position is responsible for providing QA oversight and auditing of activities related to clinical and preclinical studies. · Audit systems, studies, processes, reports, records, and data for accuracy and compliance with applicable regulations. · Detect Quality Issues and ass ...

+We are seeking a detail-oriented Quality Assurance professional to join the Merck Animal Health (MAH) Global Research and Development team. · ...

+Job Summary · This position is responsible for providing QA oversight and auditing of activities related to clinical and preclinical studies.Examples of activities within the scope of oversight and auditing include but are not limited to: preclinical animal studies, sample analy ...

The CCTRO is seeking an experience research study coordinator quality auditor who will join the CCTRO quality team and assist the team with clinical trial quality assurance and quality control activities including study auditing and monitoring as primary responsibilities but will ...

The Quality Associate tasks include: CW shadows ongoing studies and supports them to provide Quality oversight and recommend best practices. · Consults on major and critical quality issues with Senior GCP Level 1 members. · Supports risk assessments for the annual GQM Audit Plan. ...

Prepares grant applications manuscripts Institutional Review Board IRB applications research papers and assists with complex research papers. · ...

The Clinical Research Coordinator will work with investigators, study staff, and regulatory agencies to ensure compliance with study protocols and data documentation. · Schedule all protocol required evaluations (physical exams, radiology, labs). · Coordinate patient appointments ...

The CCTRO is seeking an experience research study coordinator quality auditor who will join the CCTRO quality team and assist the team with clinical trial quality assurance and quality control activities. · Perform routine monitoring of investigator-initiated trials. · Routine an ...

Manager of Clinical Quality Assurance position is an exciting opportunity to build upon solid clinical research experience to become a key member of the Clinical Quality Assurance team. · ...

+Job summary · The Quality Assurance Director ensures that all clinical trials are conducted in accordance with study protocols, · FDA regulations and ICH/GCP guidelines. · +ResponsibilitiesConduct audits of study documents. · Collaborate with Site Director and study PIs. · ...

The audit management specialist is responsible for managing the audit program and leading audits to ensure compliance and data integrity. · Minimum 3 years of relevant audit experience in a FDA Environment such as pharmaceutical or biotech company. · Comprehensive knowledge of th ...

This is a pivotal Quality Assurance role within the Global Research and Development Department at Merck Animal Health (MAH) in Rahway, NJ. · ...

As an Audit Associate in the Liverpool office, you will work closely with managers, directors and partners to deliver high-quality audits across a diverse client base. · ...

The Clinical Trials Office seeks a Clinical Research Associate to perform duties related to the coordination of clinical studies.The incumbent will work with the team to ensure the safety and well-being of trial participants and to document related data per protocols and SCI-CTO ...

The QA Auditor is responsible for ensuring the highest standards of regulatory compliance and data integrity within the facility.This role involves performing rigorous audits of laboratory processes, study data, and facility records, while managing the reporting lifecycle from in ...

We are seeking a Lead Clinical Research Coordinator (CRC) who is ready to take ownership of a new clinical research program and grow into a management role.This position offers the opportunity to be the backbone of a developing research department, balancing hands-on clinical tri ...