Clinical Research Associate 2 Fsp

Job Overview: The South African National Blood Service is seeking a highly skilled Clinical Research Associate to join our team in Centurion. As a Clinical Research Associate, you will be responsible for ensuring that clinical trials are conducted according to Good Clinical Practice (GCP) guidelines and regulatory requirements.Responsibilities:Coordinate and...

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 Summary:We are seeking a skilled Clinical Data Associate to join our team at IQVIA. As a Clinical Data Associate, you will play a critical role in ensuring the success of our clinical trials by providing high-quality data management support.Key Responsibilities:Manage data from various sources, including clinical trials and external vendors.Ensure data...

**Clinical Data Manager** **South Africa | Remote** - DFnet provides data management, biostatistics, and software development services for industry, non-profit, and academic organizations worldwide. Since 2004, DFnet’s people, products, and services have helped our global clients with over 100 Phase I through Phase IV clinical trials. Our focus is global...

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...

We are looking for a **Clinical Research Specialist** with the following key knowledge areas: - Basic understanding of evidence-based medicine. - Knowledge of health data standards. - Knowledge of “managed healthcare” or financial risk assessment principles (environment). - Knowledge of standards within the health industry. - Knowledge of the...

**Essential Functions** - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines. - Assist the clinical team with the preparation, handling, distribution,...

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 clinical...

Labcorp is looking to recruit a SCTA (CTC) to join our sponsor in South Africa! **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 o Update clinical trial databases (CTMS) and trackers - Clinical supply &...

Base level rolePerform comprehensive data management tasks including data review, query generation and query resolution. This may also include, but is not limited to creation of eCRF completion guidelines, entry of test data for eCRF and the Data Review Model, testing of data validation rules, etc. Data Management tasks should be inclusive of Study Start-up,...

As a Clinical Support Associate at Nrc, you will be an integral part of our dialysis team. Your primary responsibilities will include providing patient care, maintaining a clean and safe environment, and supporting the overall operations of our dialysis units.Key Tasks:Ensuring that patients receive high-quality care and attention.Collaborating with...

We seek a meticulous Clinical Research Coordinator to manage day-to-day activities at MECS Africa.Responsibilities:The successful candidate will be responsible for organizing and managing health information data, developing reports, and maintaining stakeholder relationships. Strong analytical skills and attention to detail are necessary.Main...

**Summary of The Position**: The Biostatistician will be responsible for biostatistical aspects, as applicable, of clinical projects undertaken by FHI Clinical, in accordance with the relevant protocol and other trial-related documentation, ICH GCP (and applicable local adaptations thereof), other local legal requirements, relevant FDA, EMA, and other...

**Work Location**:180 Garsfontein Road, Ashlea Gardens, Pretoria (hybrid after 6 months) **Job purpose**: Conduct research, bench studies, and user studies with the required documentation, to prove the efficacy of products in accordance with regulatory and legal requirements. **Requirements**: **Minimum Education**: - M.Communication Pathology in...

**Job Advert Summary**: Applications are invited for the above-mentioned position, to be filled as soon as possible. **Minimum Requirements**: - Nursing qualification. - Clinical Auditing experience - Minimum of 2 years' experience in the managed care environment **Duties and Responsibilities**: - Conduct clinical audits on claims and costs to ensure...

Job Description:As a Clinical Data Associate at IQVIA, you will be responsible for performing comprehensive data management tasks, including data review, query generation, and resolution. This role involves creating eCRF completion guidelines, entering test data, testing data validation rules, and managing freeze/lock of eCRF.Responsibilities:Perform data...

You will perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. The role may also include maintenance activities. This is not a line management position but requires...

**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 &...

IQVIA has an exciting career opportunity for a Regulatory and Start Up Specialist within our FSP Team. This position is based in South Africa and is homebased. The individual will perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating...

Qualifications and ExperienceBachelors Degree/ Advanced Diploma in Health Sciences Nursing, Pharmacy related qualification.Valid registration with the relevant Statutory body (SANC, SAPC, HPCSA etc).Certification in evidence-based medicine and/or treatment protocol development will be an added advantage.Relevant 5 - 7 years experience in a Managed Healthcare...