Senior Clinical Research Associate II

Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance...

Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance...

Job Overview Perform 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...

Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

**Job Overview** Perform 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...

**As a Statistical SAS Programmer in our Clinical Development Services (CDS) business unit, you are central to the successful delivery of complex clinical trials for renowned, innovative and global top pharmaceutical and biotech companies. Oftentimes you will have the opportunity to lead studies through various phases of the clinical development plan and...

Purpose: Provides high quality, on-time input to client projects in the life sciences field. Assignments range in complexity from primary market research, basic analysis and problem solving. Will serve as project leader for small teams or work streams. Principal Accountabilities: Assists with the review and analysis of client requirements or problems...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programs RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a key customer Ability to...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programs RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a key customer Ability to...

IQVIA South Africa has a great opportunity for a Senior MC Consultant position in our Commercial Solutions team based in Centurion. Responsible for the on-time completion of projects or components of large, complex projects for clients in the life sciences field. Identifies and elevates potential new business opportunities and assists in the sales...

P Purpose: - Provides high quality, on-time input to client projects in the life sciences field. Assignments range in complexity from primary market research, basic analysis and problem solving. Will serve as project leader for small teams or work streams. - Principal Accountabilities: - Assists with the review and analysis of client requirements or...

**Position: Senior Scientist: Chromatography - NRL Esoteric** **AREA: CENTURION** Our very well-established client is looking for a SENIOR SCIENTIST that Specialise Analytical Techniques. Technical experience with the focus on method optimization & troubleshooting. Technical training of analysts. Methodologies (Chromatography &...

IQVIA South Africa has a great opportunity for a Senior MC Consultant position in our Commercial Solutions team based in Centurion. Responsible for the on-time completion of projects or components of large, complex projects for clients in the life sciences field. Identifies and elevates potential new business opportunities and assists in the sales...

QVIA is the Human Data Science Company™ oriented to drive human health outcomes forward. By joining us as a Informed Consent Form Lead ( ICF) you will perform tasks at a global level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project...

Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance...

Applicants are required to meet the following criteria: Eng. degree in Mechanical Engineering with PrEng registration 8+ years relevant experience in the built environment (Hospitals, Clinics, Commercial Buildings, Offices, workshops, stores, etc.). Engineering experience in large projects covering relevant divisional requirements. Experience in...

Applicants are required to meet the following criteria: Eng. degree in Mechanical Engineering with PrEng registration8+ years relevant experience in the built environment (Hospitals, Clinics, Commercial Buildings, Offices, workshops, stores, etc.).Engineering experience in large projects covering relevant divisional requirements.Experience in construction...

Applicants are required to meet the following criteria: Eng. degree in Mechanical Engineering with PrEng registration8+ years relevant experience in the built environment (Hospitals, Clinics, Commercial Buildings, Offices, workshops, stores, etc.).Engineering experience in large projects covering relevant divisional requirements.Experience in construction...

Under general supervision, develop and prepare grant budgets to be included in proposals for assigned customers, to support the global sales team. IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science...