Clinical Associate

Associate Project 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 Associate Project Lead i

Job DescriptionWith support of Senior Clinical Research Associate/Clinical Research Associate and/or CRA Manager, the Associate CRA acts as primary site contact and site manager throughout all phases

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

Job DescriptionWith support of other Clinical Research Managers and/or Therapeutic Area Head/Clinical Research Director, this role is accountable for the end - to - end performance and project managem

We are looking for a Senior Regulatory Affairs Associate with working knowledge of Clinical Trial Applications (CTA) to join our team in South Africa! This role can be office based (Bloemfontein) or h

South Africa, Johannesburg - Home - BasedICON plc is a world - leading healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment driving innovation and

nd veterinary nursing students (including special emphasis on small stock/flock health management); Clinical and herd/flock health services through the Onderstepoort Veterinary Academic Hospital, surr

c and wildlife species, community and environmental health. This person will focus on the teaching, clinical service and research in fields related to veterinary reproduction.ResponsibilitiesThe succe

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

ding global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device

Job Title: Clinical Research Associate (CRA)Location: Johannesburg South AfricaCompany: ICON Strategic Solutions FSPAs a Clinical Research Associate, your primary focus will be on the end - to - end m

Description:Site Manager (Clinical Research Associate)Johnson & Johnson Innovative Medicine is recruiting for a Site Manager (Clinical Research Associate) located within commutable distance of Joh

Company: PPD, part of Thermo Fisher ScientificJob Title: Clinical Trial Associate (CRA)Countries: South AfricaLocation: Based on Preference (Remote / Hybrid / On - Site)Status: Full - time / Permanent

Company: PPD, part of Thermo Fisher ScientificJob Title: Clinical Trial Associate (CRA)Countries: South AfricaLocation: Based on Preference (Remote / Hybrid / On - Site)Status: Full - time / Permanent

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

IHCRA/in - house CRA JohannesburgICON plc is a world - leading healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment driving innovation and excellen

We are looking for an experienced Regulatory Affairs Professional with working knowledge of Clinical Trail Applications (CTA) to join our team in South Africa! This role can be office based (Bloemfont

cebased - Johannesberg/Durban or HomebasedICON plc is a world - leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing ou

nt process and development activities.INCIDENTSThe practical accompaniment of students at different clinical accredited facilities as allocated to the School of Nursing Science (Potchefstroom campus)

UP Posting - AcademicFACULTY OF VETERINARY SCIENCEDEPARTMENT OF COMPANION ANIMAL CLINICAL STUDIESSENIOR LECTURER/ ASSOCIATE PROFESSOR/ PROFESSOR: EQUINE MEDICINE (ONE POST) In pursuit of the ideals of

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

hensive trial and site administration and involves preparing, collating, distributing and archiving clinical documents. The Clinical Trial Coordinator supports clinical supply and non - clinical suppl

able for performance and compliance for assigned protocols in a country in compliance with ICH/Good Clinical Practice and country regulations, company policies and procedures, quality standards and ad

isation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touc

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

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

DescriptionYou will be permanently employed by Labcorp Drug Development working in our Clinical Development Services (CDS) division working across a wide range of Sponsors and multiple therapeutic are

DescriptionYou will be permanently employed by Labcorp Drug Development working in our Clinical Development Services (CDS) division working across a wide range of Sponsors and multiple therapeutic are

promoting protocols with us, working alongside our talented, bright and energetic teams. Our global Clinical department consists of colleagues with institutional knowledge, in - depth therapeutic expe

compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager or Clinical Research Director, the person ensures compliance of study conduct with ICH/Good Clinical Pr

RD, the person is responsible for Supporting budget/finance aspects, for execution and oversight of clinical trial country submissions and approvals.Responsibilities Include But Are Not Limited ToSupp

ry.Under the oversight of the CRA Manager, the person ensures compliance of study conduct with Good Clinical Practice and country regulations, company policies and procedures, quality standards and ad

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

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

As a Clinical Trial Associate you will be joining the worlds largest & most comprehensive clinical research organisation, powered by healthcare intelligence.Key ResponsibilitiesSupport country and sit

obal platform for the LGBTQ+ business community. Please do not contact the recruiter directly. As a Clinical Trial Associate you will be joining the worlds largest & most comprehensive clinical resear

ely status updates including issues & risks to DM and DMLs as neededAct as the Point of contact for Clinical Data Manager, working pro - actively to identify risks and provide mitigationsMay communica

ely status updates including issues & risks to DM and DMLs as neededAct as the Point of contact for Clinical Data Manager, working pro - actively to identify risks and provide mitigationsMay communica

ely status updates including issues & risks to DM and DMLs as neededAct as the Point of contact for Clinical Data Manager, working pro - actively to identify risks and provide mitigationsMay communica

nJOB PURPOSE To support in registration/approval of new products, line extensions, new indications, clinical trials, variations, support regulatory maintenance activities of the registered base portfo

nJOB PURPOSE To support in registration/approval of new products, line extensions, new indications, clinical trials, variations, support regulatory maintenance activities of the registered base portfo

Job OverviewProvide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data management products that meet customer needs. M

Job OverviewProvide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data management products that meet customer needs. M

siness One or another similar ERP system required Knowledge of foreign currency a plus Knowledge of clinical trial process a plus Strong PC skills (i.e. Microsoft Office) Strong organizational skills

ding global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device

pital (Thurso)This is an exciting post also open to recent graduates who may wish to increase their clinical skills.This post may incorporate a significant period of mentorship covering clinical techn

rea of responsibility Collects and organizes information on regulatory requirements for quality, preclinical and clinical data to meet applicable regulations. Prepares and submits regulatory submissio

s one of the largest healthcare systems in the UK employing around 40, 000 staff in a wide range of clinical and non - clinical professions and job roles. We deliver acute hospital, primary, community

s one of the largest healthcare systems in the UK employing around 40, 000 staff in a wide range of clinical and non - clinical professions and job roles. We deliver acute hospital, primary, community

isation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touc

s one of the largest healthcare systems in the UK employing around 40, 000 staff in a wide range of clinical and non - clinical professions and job roles. We deliver acute hospital, primary, community

evelopmentIn R&D, we're full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. With nine

ur career prospects. Opportunities exist for postgraduate studies that lead to rewarding careers as clinical, industrial and academic pharmacists.Main ObjectivesAll academics are responsible for disse

gulatory agenciesIQVIA 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 hu

graduate medical education.The post is part time to specifically enable the post holder to still be clinically/research active on their off days (usually Mondays) (to do locums, etc.) or do something

DescriptionRequired Minimum QualificationsClinical associate degree/ bachelors Clinical Medical Practice.VMMC Training course.Quality Improvement TrainingDesirable QualificationsClinical associate deg

A specialist Physician based in a private practice in Pretoria, is looking for a clinical nursing assistant or a clinical associate/technician who can perform general administrative duties, reception

Job title : Clinical Risk ConsultantJob Location : Gauteng, JohannesburgDeadline : April 10, 2025Quick Recommended LinksJobs by LocationJob by industries Job DescriptionClinical Risk Consultants are r

phases of the MBChB programme would require the establishment of a fully functional, world - class, Clinical Anatomy division. Therefore, the Professor/Associate Professor in Anatomy is expected to ex