Clinical research

Project Management Analysts (PMA) 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 PMA works in pa

tes based in France (good knowledge of the "convention unique" is needed). Ensure adherence to good clinical practice (GCP), standard operating procedures (SOPs), work instructions (WIs), quality of d

science a step beyond through research, development and delivery of life - changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical

science a step beyond through research, development and delivery of life - changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical

science a step beyond through research, development and delivery of life - changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical

science a step beyond through research, development and delivery of life - changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical

ICON plc is a world - leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biote

Develop and execute business development strategies tailored to the South African healthcare market.Clinical Liaison: Act as a liaison between clinical teams, sales teams, and leadership to ensure ali

ntry position dedicated to support development and implementation of emerging AI/ML technologies in clinical research protocol design. If you are interested in innovations and artificial intelligence

with the core project team. Accountable for the strategic development and execution or delivery of clinical studies in line with agreed upon contracts while optimizing speed, quality and cost of deli

with the core project team. Accountable for the strategic development and execution or delivery of clinical studies in line with agreed upon contracts while optimizing speed, quality and cost of deli

Job OverviewProject 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 ess

Job OverviewProvide management and service delivery excellence of projects, as assigned by Clinical Event Validation and Adjudication (CEVA) management, covering single or multiple EAM (Endpoint Adjud

G CLINICIAN SCIENTIST and EMERGING SCIENTISTS Location Johannesburg, ZA Organization Name School of Clinical Medicine Department DescriptionEMERGING CLINICIAN SCIENTIST and EMERGING SCIENTISTS .AC05/A

Job OverviewThe Forecast Analyst is responsible for becoming the subject matter expert for IQVIAs Clinical Trial Payment departments forecasting service and for driving the quality of forecast for the

n?Skilled at software and computer use, that enjoys technology applied to data analysis?Understands clinical trial conduct, and skill in applying applicable clinical research regulatory requirements a

n?Skilled at software and computer use, that enjoys technology applied to data analysis?Understands clinical trial conduct, and skill in applying applicable clinical research regulatory requirements a

n?Skilled at software and computer use, that enjoys technology applied to data analysis?Understands clinical trial conduct, and skill in applying applicable clinical research regulatory requirements a

ela School of Medicine in Durban, South Africa and undertakes research in HIV, TB and COVID at four clinical research sites in KwaZulu Natal.CAPRISA's goal is to undertake globally relevant and locall

Senior Clinical Data CoordinatorICON plc is a world - leading healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment driving innovation and excellenc

reMinimum Required Education And ExperienceTypically requires 3 - 5 years of relevant experience in clinical research. Equivalent combination of education, training and experience.Requires intermediat

ng plays a critical role in overseeing the delivery of accurate and timely payments forecasting for clinical studies contracted for this service. This global role involves managing a team of Forecast

ks independently under limited supervision. Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects.Resp

istrative teams makes sure our concepts become reality.The successful incumbent will support Global Clinical Trial Operations (GCTO) department in South Africa including the following responsibilities

science a step beyond through research, development and delivery of life - changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical

perience6 - 8 years Managed Care experience preferredAccountabilitiesContinuous improvement:Provide clinical inputs on ex - gratia funding requestsOpen, review and resolve all clinical queries and ass

from HCPs and customers.Ensure appropriate medical governance oversight and risk management for all Clinical studies conducted in the country, and that subjects and patients are not placed at unnecess

science a step beyond through research, development and delivery of life - changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical

perience6 - 8 years Managed Care experience preferredAccountabilitiesContinuous improvement:Provide clinical inputs on ex - gratia funding requestsOpen, review and resolve all clinical queries and ass

The IQVIA Global Site Activation team is one of the clear market leaders in Clinical Trial Site Activation, driving best in class employee, site and customer experiences. This position can be anywhere

The IQVIA Global Site Activation team is one of the clear market leaders in Clinical Trial Site Activation, driving best in class employee, site and customer experiences. This position can be anywhere

tics helps interpret and draw inferences from data collected on patients as they progress through a clinical trial and serves as the bridge between data capture and reporting.We have one of the larges

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programs.ResponsibilitiesActs as a Clinical Trial

ilities: Welcoming and assisting patients in a professional and compassionate manner Assisting with clinical procedures and patient care under supervision Coordinating appointments and managing electr

biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.O

g the development and execution of Proposals or Contracts. You will receive a good grounding in the Clinical Research industry, as well as project management skills, financial fundamentals, negotiatio

ced scientific exchanges with key external stakeholders by maintaining relevant, robust and current clinical / scientific knowledge of healthcare landscape and therapeutic area expertise. Ensures all

ding of the fundamental processes of business and the impact of the external/internal influences of clinical decision making.Experience in the management of medical protocols and the development and m

world. Every day our team develops evidence - based strategies that are used in published research, clinical guidelines, and market access decisions, to improve healthcare at every touchpoint. We desi

rnational relationships to contribute to understanding of diseases, research and scientific trends, clinical practice guidelines, treatment patterns in areas relevant to our business.Serve as a condui

lth promotion.ResearchHave published research articles in recognised and refereed movement science, clinical or health - related journals, with a focus on clinical research or movement education.Provi

ela School of Medicine in Durban, South Africa and undertakes research in HIV, TB and COVID at four clinical research sites in KwaZulu Natal.CAPRISA's goal is to undertake globally relevant and locall

ting as a lead on studies, you will directly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines and

PPD, now Thermo Fisher's clinical research business, is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management servic

Main Purpose Of The JobTo compile source documentation for the collection of clinical research data and ensure that clinical research data is entered into the data entry system timely, accurately, and

Senior Statistical ProgrammerICON plc is a world - leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced serv

e to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements.Assist with the creation an

e to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements.Assist with the creation an

Senior Operation Program Specialist - EMEAICON plc is a world - leading healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment driving innovation and

e Client Services Associate is managing core financial data implementation for contracts with CROs, clinical sites, clients and investigators and oversees the site reimbursement process of invoicing a

IA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory submi

point statistical programmers at Principal level to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory submi

xible and creative leadership through collaboration.Associate Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients lives by bringing new drug

very function, enabled by best - in - class technology and data analytics.Key collaborators are the Clinical Lead for site management, the Project Vendor Manager, the Project Management Analyst for pr

ime and within budget, to customer satisfaction. Provide comprehensive data management expertise to Clinical Data Management (CDM) team to provide high quality data management products that meet custo

ance with sponsor Procedural Documents, ICH - GCP and local regulations. Ensures, as required, that clinical and operational feasibility assessment of potential studies is performed to the highest qua

(ICF) and Investigator Pack (IP) release documents.Qualifications And SkillsGrade 12 with 1 - year clinical research, administrative or other relevant experience a healthcare environment or equivalen

ationsBachelor's Degree Computer Science, a related field, or equivalent experienceUnderstanding of Clinical trials is requiredExperience with Clinical research and eSource platform is preferredExperi

ationsBachelor's Degree Computer Science, a related field, or equivalent experienceUnderstanding of Clinical trials is requiredExperience with Clinical research and eSource platform is preferredExperi

as a Nurse Consultant with responsibilities related to the management, evaluation, and oversight of clinical and operational activities that are part of broad national VHA medical center programs supp