Clinical researchJob search results in: Jobs in Cape Town

OverviewIQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture

s Council of South Africa (HPCSA) or the South African Nursing Council (SANC) - (Desirable)KnowledgeClinical knowledge (e.g., knowledge of anatomy and physiology, which helps in understanding medical

ion focused on African genomics. Join us to leverage our extensive genetic, genomic, proteomic, and clinical data repositories with a focus on unique datasets generated through the Roche African Genom

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

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

mization Specialist to join our team and contribute to the planning, execution, and optimization of clinical trials. This role involves analyzing data, identifying key insights, and implementing strat

terial for online access.Supervision of internsMinimum RequirementsMasters degree in Counselling or Clinical PsychologyRegistered with the HPCSA as a Counselling or Clinical PsychologistMinimum of 3 y

/ specialist setting, within the anaesthetics arena.Strong understanding of anaesthetics within the clinical environment.Established relationships with KOLs within the Western and Easton Cape territor

agenda, advocating for equal access to quality healthcare for all, and fostering the advancement of clinical practice and health policy. They will build solid relationships with research communities t

ster and escalating critical issues to senior management when necessary.Ensure compliance with Good Clinical Practice (GCP), company SOPs, and regulatory guidelines.Prepare and deliver status reports,

erating procedures and work instructions and the ability to apply them in practiceKnowledge of Good Clinical Practices and relevant regulatory guidelinesExcellent communication, interpersonal, custome

are seeking an experienced and strategic leader to join our team in Africa as a Senior Director of Clinical Operations. In this role, you will direct a team of clinical staff across a designated grou

nstitute, or equivalent.An understating of NHREC requirements and standards, guidelines relevant to clinical and research ethics.Proven report writing and minute - taking skills and working ability of

ient needs, is a role model in the delivery of evidence based care and will actively participate in Clinical Governance.ResponsibilitiesAudit of health records and implementation of corrective action

he collaborative agreement with the Provincial Health Department. This includes contributing to the clinical service delivery component, in line with the requirements of the service delivery model. Th

process Actively participate in ongoing and required knowledge assessments pertaining to strategy, clinical trials, product and competitor with an achievement of required company pass rates (80%) Tak

ation and analysis.        Combine qualitative results with clinical, demographic, and geographic data for integrative analysis.     &n

or as part of a team.An understanding of NHREC requirements, standards, and guidelines relevant to clinical and research ethics.Demonstrated experience and competence in the preparation of agendas an

process Actively participate in ongoing and required knowledge assessments pertaining to strategy, clinical trials, product and competitor with an achievement of required company pass rates (80%) Tak

g processActively participate in ongoing and required knowledge assessments pertaining to strategy, clinical trials, product and competitor with an achievement of required company pass rates (80%)Taki

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

sector expertise to increase the sustainability of the global healthcare system from early - stage clinical research, to acute and palliative care.Every day you willUse a centralised software deploym

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

support as requiredAct as a point of escalationQualifications Experience with ICF writing 1 year of clinical research experience in similar role at minimum or equivalent combination of education, trai

al Work at both Head Quarters and SitesAdvantageousExperience working in a research environmentGood Clinical Practice (GCP) CertificateAdvanced/Evasive Driving Course CertificationDangerous Goods Cert

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

iotherapy or any other relevant qualificationAt least 2 years assessment experienceAt least 3 years clinical experienceExcellent oral and written communication skillsAbility to produce quality work in

ng future.Minimum RequirementsThe main purpose of the position is to render efficient and effective clinical care to volunteers on research studies and clients at the Youth Centre. Please include a co

process Actively participate in ongoing and required knowledge assessments pertaining to strategy, clinical trials, product and competitor with an achievement of required company pass rates (80%) Tak

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

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

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

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

ssionate about how technology can help progress your profession?If you have experience working in a clinical or high - performance setting and are a physiotherapist, athletic trainer, or strength and

insight/expertise to the Business Development and Scientific Strategies teams for the potential new clinical trial projects involving a genetic scope. The genetic scopes involves fee - for - service a

ncy, management of data analytics and customer relationship interactions. These services ensure our clinical research activities are of the highest quality. We proactively support our business partner

a venture - backed technology startup on an unstoppable mission to disrupt patient recruitment for clinical trials, a $100 billion dollar sector. Clinical trials need millions of qualified patient vo

aintain effective working relationships and communicate regularly with a wide range of individuals, clinical and non - clinical, internal and external to UKHSA.The duties/responsibilities listed above

Position: Group Financial ManagerLocation: Cape Town (office based)Our client is an international clinical research organization dedicated to enhancing global health and is seeking an ambitious and dr

aintain effective working relationships and communicate regularly with a wide range of individuals, clinical and non - clinical, internal and external to UKHSA.The duties/responsibilities listed above

aintain effective working relationships and communicate regularly with a wide range of individuals, clinical and non - clinical, internal and external to UKHSA.The duties/responsibilities listed above

aintain effective working relationships and communicate regularly with a wide range of individuals, clinical and non - clinical, internal and external to UKHSA.The duties/responsibilities listed above

aintain effective working relationships and communicate regularly with a wide range of individuals, clinical and non - clinical, internal and external to UKHSA.The duties/responsibilities listed above

aintain effective working relationships and communicate regularly with a wide range of individuals, clinical and non - clinical, internal and external to UKHSA.The duties/responsibilities listed above

aintain effective working relationships and communicate regularly with a wide range of individuals, clinical and non - clinical, internal and external to UKHSA.The duties/responsibilities listed above

aintain effective working relationships and communicate regularly with a wide range of individuals, clinical and non - clinical, internal and external to UKHSA.The duties/responsibilities listed above

n integral part of cross - functional brand team through the development working relationships with clinical, medical, regulatory affairs, sales and finance departmentsDevelops relations with Sales Ma

Manage engagement with external stakeholders relating to Medical Intelligence to understand current clinical practices, obtain medical guidance and maintain up - to - date knowledge in respective ther

n integral part of cross - functional brand team through the development working relationships with clinical, medical, regulatory affairs, sales and finance departments Develops relations with Sales M

a venture - backed technology startup on an unstoppable mission to disrupt patient recruitment for clinical trials, a $100 billion dollar sector. Clinical trials need millions of qualified patient vo

ification and procurement of an Electronic Health Records (EHR) system, as well as other IT related clinical applications, that meet the nursing end user as well as company clinical and patient care n

PURPOSE Site Enablement Solutions Lead (SESL) supports clinical study sites by providing two tailored services to sites:In collaboration with Patient Recruitment & Enablement (PRE) Team, SESL supp

ct work estimates and defined delivery methods.Works in conjunction with internal project managers, clinical application consultants, field service engineers, senior Technical Consultants, third - par

llsLateral creative thinkingAdaptive to change Ability to multi - taskAdvantageousKnowledge of Good Clinical Practices and Human Subjects Protections in researchValid code 8 drivers licensePrevious el

projects and grants, and provide financial administration support to Project Leaders and on - site clinical research staff. The ideal candidate should be professional, organised and capable of dealin

a venture - backed technology startup on an unstoppable mission to disrupt patient recruitment for clinical trials, a $100 billion dollar sector. Clinical trials need millions of qualified patient vo

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

igator(s), to lead the study site teams, manage day - to - day activities of the study, and provide clinical guidance in the management of patients with HIV - associated cryptococcal meningitis partic

a venture - backed technology startup on an unstoppable mission to disrupt patient recruitment for clinical trials, a $100 billion dollar sector. Clinical trials need millions of qualified patient vo

ling. Risk identification and mitigation as it relates to but not limited to Fraud waste and abuse. Clinical predictor analytics as it relates to medical risk factors and early detection of possible c