Investigator

have the right capabilities and information to perform their duties.You will identify and map KOLs, investigators and research centres within the relevant therapy areas. Close collaboration with clini

Closing Date 2024/09/06Reference Number MMH240827 - 4Job Title Personal Lines Claims Investigator (KZN)Position Type PermanentRole Family Client ServicesCluster Momentum Insure Company LimitedRemote O

cal Director provides medical and scientific support to clinical research programs, study teams and investigators. The Medical Director also provides review, advice, and leadership for potentially or

ormed to the highest quality. Coordinates the site selection process by identifying potential sites/investigators, performing initial Site Quality Risk Assessment, and conducting Site Qualification Vi

responsibilities assigned to role are outlined in the task matrix. Essential Functions: - Monitors investigator sites with a risk - based monitoring approach: applies root cause analysis (RCA), criti

ies assigned to role are outlined in the task matrix.Essential Duties and Responsibilities:Monitors investigator sites with a risk - based monitoring approach: applies root cause analysis (RCA), criti

ents (e.g., patient diaries, instructions).Document proper destruction of clinical supplies.Prepare Investigator trial file binders.Obtain translations of documents. Regulatory & Site Start - Up r

vity Monitoring and Closeout: Perform routine tasks across assigned studies including site loading, Investigator Portal access, kit shipments, monitoring day - to - day study performance, overseeing L

pections, etc. Active interactions with external stakeholders during various meetings (e.g. meeting Investigators during various site visits, local Investigator meetings, local congress, etc.) and man

participant flow in the clinicClinical trial oversight or management as designated by the Principal InvestigatorParticipation in all phases/components of the research processData management excellence

ility - based and field - based staff and project logisticsWorking closely with the project Primary Investigator, Operations Manager, Primary Project Leads and Data Manager to ensure project governanc

vity Monitoring and Closeout: Perform routine tasks across assigned studies including site loading, Investigator Portal access, kit shipments, monitoring day - to - day study performance, overseeing L

lized Monitoring requirements.Perform routine tasks across assigned studies including site loading, Investigator Portal access, kit shipments, monitoring day - to - day study performance, overseeing L

y when requiredMust be able to work well under pressure and achieve deadlines.THE HATS YOU MAY WEAR Investigator: able to identify problems/concerns with execution of a job and inform relevant parties

ord About us: Leibold Consulting & Services (PTY) LTD was registered in 2004 as a Detective and Investigator consultancy. At the end of 2012 a strategic decision was made to broaden the services f

ted, motivated, suitably qualified and experienced clinician is required to work with the Principal Investigator and Clinical Site Research Leader in managing the clinical aspects of HIV prevention tr

ES ITS PEOPLE AND PROVIDS CAREER GROWTH AND OPPORTUNITIES. OTHER RELATED: NURSE - HEALTHCARE. CLAIMS ASSESSOR. CLAIMS VALIDATOR. MERIT INVESTIGATOR. Submit CV and current earnings plus expectations 

rsity degree in journalism/ law; Email CV or WhatsApp for fast response. About company: TLD PRIVATE INVESTIGATOR provides private investigation services for individuals, Insurance companies, law firms

ni Baragwanath Academic Hospital Soweto, JohannesburgKey Performance AreasOversight of clinical and investigator - led trialsAssist research administration manager with oversight of all trials in conj

A vacancy exists for a Armoury Auditor / Investigator at our Robertville Branch reporting to the National Armoury Manager. The overall purpose of this position is to ensure that the company policies a

Main Purpose Of The JobUnder direct supervision of the study principal investigator(s), to lead the study site teams, manage day - to - day activities of the study, and provide clinical guidance in th

Ps, ICH GCP guidelines, appropriate regulations, ICON systems and the principles of and assist with investigator recruitment Maintain timelines and ensure accuracy and completeness of data entered int

ions and advisory boards.Identify and develop speakers for the companys TAs & products.Identify investigators appropriate for clinical trials.Act as a conduit for unsolicited, investigator - initi

and the clinical trial project management process, with a special emphasis on early phase studies, investigator sites and capabilities.EducationA university/college degree (preferably in Life Science

gress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents.Qualifications And SkillsGrade 12 with 1 - year clinical re

Clinical research and development Explains ongoing research programs and future developmentsManages Investigator Sponsored Study, assesses study proposals, and recommends a decision on these proposals

line with the study protocol. The Project Coordinator will work with the Project Manager and Study Investigator to oversee project staff performing participant screening and consenting, and data coll

ion activities.Discussing research projects with external experts in case its needed.Facilitate the Investigator Initiated Trail (IIT) process in case its needed.Discussion of developmental studies or

Our teams are growing!We are looking for a Clinical Operation Manager | Investigator Site Contracts Manager to work fully dedicated to one of our biggest sponsor.You will perform tasks at a country le

required documents such as questionaires, CDAs, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents. Requires advanced knowledge within a specific discipline t

required documents such as questionaires, CDAs, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents. Requires advanced knowledge within a specific discipline t

al development organizations Manage the field activities related to the submission and execution of Investigator Supported Studies (ISS) in line with Aspens existing policiesProvide scientific support

ay participate in site feasibility and/or pre - trial site assessment visitsAttends/participates in investigator meetings as needed.Responsible for performing activities within site initiation and sta

pections, etc. Active interactions with external stakeholders during various meetings (e.g. meeting Investigators during various site visits, local Investigator meetings, local congress, etc.) and man

engineer(loss prevention) to join their team .Following are the open positions under safetyIncident Investigator Safety engineer Safety Advisor Technical safety (Process safety )Your primary role as a

as determined by the Sponsors requirements.Essential FunctionsDevelop Coordinate the development of investigator grants and estimates, contracting strategies and proposal text to support the proposal

ldExperience DetailsWorking knowledge of clinical trial process, ideally with specific knowledge on investigator contracts and essential site documents;Experience in financial forecast and accrual rep

as determined by the Sponsors requirements.Essential FunctionsDevelop Coordinate the development of investigator grants and estimates, contracting strategies and proposal text to support the proposal

uct audits supporting the Internal Audit team. Conduct internal investigations when appointed as an investigator. Provide timely and adequate input for the reporting and other reporting requirements.

measurable, achievable recommendations/actions to prevent recurrence. Support and mentor line area investigators, monitoring progress, ensuring investigative standards are met and that root cause has

case authoring and UAT executionResponsible for creating site and subject facing documentation like Investigator Manuals, Patient Facing Guides, Site reference guidesResponsible for project managing t

case authoring and UAT executionResponsible for creating site and subject facing documentation like Investigator Manuals, Patient Facing Guides, Site reference guidesResponsible for project managing t

g and analysing information, asking the right questions, and thinking things through.Fact - Focused Investigator: You prioritise finding and documenting facts to understand the logic behind any proble

ensure that patients remain the ultimate focusAppropriately provide Medical support throughout the Investigator Sponsored Research (ISR) processCultivate research and therapeutic area expertise, incl

elines are met (for example, filing and archiving of study documentation, dispatching of queries to investigator sites for resolution, etc.).Mentor junior data coordinators, providing expert guidance

cedure and/or law of evidence.5 years practical experience as an attorney/advocate OR as a forensic investigator with full ICFP membership.A proven research track record with publications in accredite

Chair for Precision Medicine and Genomics in Africa is an opportunity for an energetic mid - career investigator to advance their career as an international leader in the fields of precision medicine

gy improvements and standards to enhance quality, increase productivity (internal and external with Investigator sites) and reduce data latency within Quintiles clinical trial systems inclusive of IVx

ns learned, best practices and frequently asked questions at the trial level.Presents and trains at investigator and monitor meetingsEducation/ExperienceBS/BA degree or higher preferably in Health Sci

cialists for assigned studies.Coordinates the site selection process by identifying potential sites/investigators, performing initial Site Quality Risk Assessment, and conducting Site Qualification Vi

ress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines.Provide local expertise to

of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form, and Investigator Pack release documents.You will also support the updating and maintenance of internal s

idence to support criminal investigation and/or legal action. Recommend further actions to the lead investigator.Fraud/Financial Crime ManagementAnalyze data to identify and track and report key trend

or Advanced Diploma) related qualification to discipline.Driver's License.Completed training as an investigator will be an added advantage.Being a certified fraud examiner will be an added advantage.

, stratified by original research and other.A description of previous grants secured as a Principal InvestigatorResearch plan (3 - 5 pages)A maximum 10 publications (pdf) to be considered in the asses

eetings, coordinating correspondence, and supporting budget tracking.Assist with the preparation of investigator meeting materials and local logistical arrangements.Participate in the archiving of tri

eetings, coordinating correspondence, and supporting budget tracking.Assist with the preparation of investigator meeting materials and local logistical arrangements.Participate in the archiving of tri

emergency management, stabilizing services in crisis and turnaround project management.Experienced investigator, planner and implementer.CareTech Community Services Ltd is a provider of specialist so

tion plans, maintain updated risk registers, and ensure preventative controls are in place.Incident Investigator: Lead or support incident investigations and implement corrective actions to prevent re