Senior Manager, Clinical Trials- Radiopharmaceuticals - Paramus, New Jersey, United States

The SCTM (Senior Clinical Trial Manager) supporting Radiopharmaceuticals will be independently responsible for ensuring the execution of more complex clinical studies in one or more geographic regions in Phases I–IV, in adherence to Good Clinical Practices (GCPs), appropriate SOP ...

Overview: · The SCTM (Senior Clinical Trial Manager) supporting Radiopharmaceuticals will be independently responsible for ensuring the execution of more complex clinical studies in one or more geographic regions in Phases I–IV, in adherence to Good Clinical Practices (GCPs), app ...

Auditor with experience in pharmaceutical industry and radiopharmaceuticals required. · Bachelor's degree in a scientific, health care, or related discipline. · Minimum 5+ years of experience in the pharmaceutical industry. · ...

We are seeking an experienced GCP Quality Assurance Auditor to join our rapidly growing biopharmaceutical company specializing in neurology and psychiatry therapies. · This role ensures GXP compliance drives quality management initiatives conducts internal external auditsacross c ...

The company is seeking to add a GCP Quality Assurance Auditor to their team.This position will be focused on ensuring GXP compliance with regulatory authorities and driving the Company's compliance directives and supporting quality management systems. · ...

The GCP Quality Assurance Auditor will report to the Director the GCP/PVG Quality Assurance and ensure GXP compliance with regulatory authorities. · ...

The GCP Quality Assurance Auditor will report to the Director of GCP/PVG Quality Assurance. This position will ensure GXP compliance with regulatory authorities, drive and implement compliance directives, and support quality management systems. · ...

We are seeking an experienced GCP Quality Assurance Auditor to play a key role in ensuring GXP compliance across global clinical programs. · Plan and conduct global clinical process audits and clinical vendor audits across all phases of clinical trials. · ...

· Our client is seeking an experienced GCP Quality Assurance Auditor to play a key role in ensuring GXP compliance across global clinical programs, with a specialized focus on radiopharmaceutical development. This role supports clinical operations, non‑clinical functions, and ma ...

+We are seeking an experienced GCP Quality Assurance Auditor to support quality and compliance initiatives within a regulated biopharmaceutical environment.+ · +Ensure GxP compliance with global regulatory requirements. · Strengthen quality management systems (QMS). · +This role ...

The GCP Quality Assurance Auditor will report to the Director the GCP/PVG Quality Assurance. · Plan and conduct scheduled global clinical process and clinical vendor audits across all clinical trials. · Plan and conduct audits of specific clinical processes based on risk. · ...

We are seeking an experienced GCP Quality Assurance Auditor to support quality and compliance initiatives within a regulated biopharmaceutical environment. · This role focuses on ensuring GxP compliance with global regulatory requirements, strengthening quality management systems ...

+Plan and conduct scheduled global clinical process and clinical vendor audits across all clinical trials+ · +Perform clinical vendor audits along with various SMEs (IRT, EDC etc.) to comprehensively assess all services provided by a vendor+ · +Review, understand, and audit clini ...

The GCP Quality Assurance Auditor will report to the Director GCP/PVG Quality Assurance ensuring compliance with regulatory authorities driving and implementing companys compliance directives supporting quality management systems. · Plan conduct scheduled global clinical process ...

The GCP Quality Assurance Auditor will report to the Director and ensure GXP compliance with regulatory authorities. · Plan and conduct scheduled global clinical process audits. · Develop audit reports and distribute them to stakeholders. · Review clinical related regulations and ...

A growing biopharmaceutical organization is seeking a GCP Quality Assurance Auditor to support global GXP compliance across clinical development, safety/pharmacovigilance, and vendor oversight. · ...

The GCP Quality Assurance Auditor will report to the Director of GCP/PVG Quality Assurance. This position will ensure GXP compliance with regulatory authorities and support quality management systems.Plan and conduct scheduled global clinical process and clinical vendor audits. · ...

· JOB DESCRIPTION: · The GCP Quality Assurance Auditor will report to the Director the GCP/PVG Quality Assurance. This position will be focused on ensuring GXP compliance with regulatory authorities, driving and implementing the Company's compliance directives and supporting qua ...

The GCP Quality Assurance Sr. Auditor will report to the Director the GCP/PVG Quality Assurance. · Plan and conduct scheduled global clinical process and clinical vendor audits across all clinical trials. · Plan and conduct audits of specific clinical processes based on risk. · ...

JOB DESCRIPTION: The GCP Quality Assurance Auditor will report to the Director the GCP/PVG Quality Assurance. This position will be focused on ensuring GXP compliance with regulatory authorities, driving and implementing the Company's compliance directives and supporting quality ...