Clinical Trials Assistant

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...

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...

**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...

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...

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...

Job Overview Perform monitoring and site management work for a variety of protocols, site and therapeutic areas. Essential Functions - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International...

**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...

Advert Reference: P7987 Project Co-Ordinator: ACT - Centurion Job Title: Project Co-Ordinator: ACT - Centurion Closing Date: 2023/12/01 Position Available From: 2023-11-27 Area: Centurion Actual Place Of Work: Centurion Position Type: Full-Time Weekly Hours: 40 Time Conditions: 5 day Work Week (South Africa) Purpose of Position: To coordinate the...

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 Under general direction, manage all laboratory aspects of assigned clinical trial projects for a Customer or a specific program for a Customer. May have responsibility for a specific Customer, drug program, indication or drug compound. Acts as the main point of contact for the Customer after study award and throughout the entire study lifecycle...

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...

Site Activation Manager Global Site Activation - GSA The GSA unit within IQVIA has the vision to be the clear market leader in clinical trial site activation, driving best in class employee, site and customer experiences and we are looking for passionate people to join our team. The Site Activation Manager (SAM) position within GSA team in IQVIA is our...

Overview: The Project Services Intern will provide support to the Project Team and related team members by performing generic procedures and tasks associated with the day to day running of projects throughout the entire study lifecycle (e.g., start-up, maintenance, and close-out); Ensure work is conducted in line with standard operating procedures, policies,...

**18th March, 2023**: **Responsibilities**: - Deliver effective pharmaceutical care in both hospital and retail environments. - Ensure effective management of patient pharmaceutical care in the absence of the Pharmacy Manager and the Operational Assistant Pharmacy Manager. - Maintain pharmaceutical standards, quality assurance, and risk management within...

We are seeking an Assoc. Lab Project Services Managerto join Q2 Solutions, IQVIA’s laboratory business in the UK or other location in EMEA. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and...

WE ARE HIRING //We are expanding our national footprint and looking for concierges to join our team at META-CLINIC Pretoria.The following are the duties and responsibilities required by the concierge to ensure the smooth and effective operation of Meta-Clinic: Manage the opening and closing of Meta-Clinic, including locking the facility. Ensure accurate...

Our Project Leadership Interns are an integral part of our global team and work in partnership with Project Management Analysts and Project Leaders in one of our therapeutic areas including Internal Medicine, Central Nervous System, Gastroenterology, Immunology & Women’s Heath, Cardiovascular Renal Metabolic, Early Phase Oncology and Late Phase...

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...