Clinical Research Associate

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 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 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...

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 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...

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...

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...

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...

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...

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...

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...

**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...

Our client is a well-established medical group of companies in Irene, Centurion. They are looking for a **QA and Regulatory Officer** to join their dynamic team. **Qualifications**: Tertiary degree required in the Natural Sciences or Engineering Minimum of 2 Years working experience **Competencies**: - Good communication skills in writing, presentation,...

My client - a leader in Financial Advisory is looking for a Development Economist. Must have Advanced Degree (Economics) with minimum 5 years experience providing advise and solutions to government and private sector clients & sourcing and leveraging data for cost-benefit analysis. You will be involved in: - undertaking the economic analysis workstream of...

Our client is searching for a Pharmacovigilance Physician to join their team in Irene Centurion.  Job Profile  This role will play a key role in bringing deep clinical understanding and judgement in benefit-risk assessments for the Organisation and their Client’s products. This role will support the medical components of Pharmacovigilance (PV) for the...

Our client is searching for a Pharmacovigilance Physician to join their team in Irene Centurion. Job Profile This role will play a key role in bringing deep clinical understanding and judgement in benefit-risk assessments for the Organisation and their Client’s products. This role will support the medical components of Pharmacovigilance (PV) for the...

Our client is searching for a Pharmacovigilance Physician to join their team in Irene Centurion. Job Profile This role will play a key role in bringing deep clinical understanding and judgement in benefit-risk assessments for the Organisation and their Client’s products. This role will support the medical components of Pharmacovigilance (PV) for the...

Qualifications:Tertiary degree required in the Natural Sciences or EngineeringMinimum of 2 Years working experienceCompetencies:Good communication skills in writing, presentation, and interpersonal communication (Good writing skills is essential)High ethical standardsGood understanding of statisticsComputer literate: Microsoft OfficePrimary...