Clinical Project Coordinator: Drive Study Timelines

**Summary of the Position**: The Clinical Research Associate II (CRA II) manages clinical study sites and monitors site activities to assure adherence to Good Clinical Practices (GCPs), Standard Operating Procedures (SOPs), study protocols, and applicable regulatory requirements. Reviews regulatory documents as required and prepares site visit reports. May...

Job OverviewIQVIABiotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative treatments to patients faster.The Clinical Project...

Job Overview IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. Agile structure, collaborative culture, and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative treatments to patients faster. The Clinical Project...

A global leader in clinical research services is seeking a Project Lead in Centurion, Gauteng. You will oversee the delivery and management of clinical studies, ensuring project quality and financial success. Ideal candidates have a Bachelor's degree in life sciences and at least 5 years of relevant experience, including project management. Strong knowledge...

Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients' lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and...

**Job Overview** Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs,...

**Summary of The Position**: The Statistical Programmer will perform statistical and database programming (typically in SAS) related to clinical projects undertaken by FHI Clinical, according to the relevant trial protocol and other trial-related documentation, ICH GCP (and local adaptations thereof), local legal requirements, relevant FDA, EMA, and other...

**Summary of The Position**: The Contract Statistical Programmer will perform statistical and database programming (typically in SAS) related to clinical projects undertaken by FHI Clinical, according to the relevant trial protocol and other trial-related documentation, ICH GCP (and local adaptations thereof), local legal requirements, relevant FDA, EMA, and...

Typical Accountabilities - Has the overall responsibility for the study commitments within the country and for timely delivery of data to required quality. - Leads Local Study Team consisting of CRA(s), CSA(s), for assigned study/studies - Leads and optimizes the performance of the Local Study Team(s) at country level ensuring compliance with sponsor...

**ASSIGNMENT PROFILE** **Clinical Trial Coordinator (CTC)** **Description of Roles and Responsibilities** - **Trial and site administration**: - Tracking (e.g. essential documents) and reporting (e.g. Safety Reports) - Ensure collation and distribution of study tools and documents - Update clinical trial databases (CTMS) and trackers - Clinical supply &...