Investigators

We have job vacancies for Private Investigators/Detectives. Positions available, Must have: Own Reliable Vehicle Experience in Private Investigations Start Immediately Basic Salary of R12 800 with pet

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

- led trialsAssist research administration manager with oversight of all trials in conjunction with investigators and study coordinatorsProvide comprehensive support of all operational aspects of tria

s. Regulatory & Site Start - Up responsibilitiesIn a timely manner, provide to and collect from investigators forms/lists for site evaluation/validation, site start - up and submissions.Obtain, tr

ifies and shares best practices. Responsible for collaboration with functional outsourcing vendors, investigators, other external partners in assigned studies. As a customer - facing role, this positi

ations of counterfeit selling/manufacturing of parts in for the assigned market;Assist a network of investigators to address counterfeit activities.Coordinate third party covert investigations and coo

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

al commitments and objectives especially during study start - up. Required to in/directly influence investigators, external partners and country operations and adheres to budget targets and agreed pay

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

al commitments and objectives especially during study start - up. Required to in/directly influence investigators, external partners and country operations and adheres to budget targets and agreed pay

er grade level, performing duties such as:Supervising supervisory and/or non - supervisory criminal investigators, with oversight of complex and sensitive criminal and administrative investigations; p

ss.Must meet and maintain medical requirements as stated in the TSA Medical Guidelines for Criminal Investigators.Physical Demands: Must be able to perform the essential job functions described in the

emptions apply). You must have a valid driver's license prior to your final job offer. ICE Criminal Investigators may use deadly force when necessary, in accordance with the law and agency policy. You

emptions apply). You must have a valid driver's license prior to your final job offer. ICE Criminal Investigators may use deadly force when necessary, in accordance with the law and agency policy. You

emptions apply). You must have a valid driver's license prior to your final job offer. ICE Criminal Investigators may use deadly force when necessary, in accordance with the law and agency policy. You

emptions apply). You must have a valid driver's license prior to your final job offer. ICE Criminal Investigators may use deadly force when necessary, in accordance with the law and agency policy. You

ebacksLiaising between various internal and external stakeholders including legal, law enforcement, investigators, banks and victimsReviewing alerts, accounts and transactions for potentially fraudule

methodologies;Mentoring and assisting in the professional development of less experienced criminal investigators; andAssessing and evaluating performance and providing feedback on employee developmen

l or electronic evidence to support criminal investigation and/or legal action, engaging specialist investigators or subject - matter experts where necessary. Review the evidence gathered and recommen

y network to mobilize fraud prevention and prosecution efforts On determined fraud cases work Fraud Investigators and law enforcement officials to ensure successful prosecution of perpetrators Qualifi

eld. To maintain 24 - hour communication with all sites and with all supervisors/reaction officers, investigators and managers. Supervise control room vehicle tracking and guard patrol system to insur

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requirements.Ability to write scientific documents e.g. Investigational Medicinal Product Dossier, Investigators Brochure, clinical trial justifications with minimum support of senior staffInteracts

ministration, liaising with service providers. Handling of admin and/or call requests from outlying investigators. Handling and resolving all queries and problems from any service providers and/or cli

d/or enhanced processes that will improve the functioning of stakeholders' businesses.Interact with investigators and external stakeholders to gain an understanding of their analytical support request

atory documentation for study start - up, study maintenance and study close - out.Communicates with Investigators and site staff on issues related to protocol conduct, recruitment, retention, protocol

is managing core financial data implementation for contracts with CROs, clinical sites, clients and investigators and oversees the site reimbursement process of invoicing and accounts payables. This p

t applications.Stay abreast with relevant data analysis advances and collaborate closely with other investigators on related studies.Publish scientific publications.Compile conference presentations.Su

ompleteness of data entered into ICON systems Serve as the primary in - house contact for sites and investigators participating in studies Conduct and completes remote site management activities, with

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

ly.Identify potential research gaps and lead/contribute to local post market studies ( contact with investigators, creation and validation of study design, study monitoring, results analysis, etc.).He

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

nce systems. Support of local regulatory and financial compliance. Ability to communicate well with investigators, external partners and country operations and adheres to budget targets and agreed pay

, economical and expeditious manner.Working in a team of experienced lawyers, financial planner(s), Investigators and negotiators.Training on the financial planning process, insurance, investments, re

apy areasDevelop and maintain contacts with key opinion leaders (local and international), clinical investigators, policy makers and all potential stakeholders that influence the businessCollaborate w

fraud;Liaising between various internal and external stakeholders including legal, law enforcement, investigators, banks and victims; Reviewing accounts and transactions for potentially fraudulent act

ten virtual, multi - cultural, and multi - disciplinary Serves as the primary contact for sites and investigators participating in studies Conducts and completes remote site management activities, wit

ves to detect and prevent abuse.Your mission will involve:Hire, mentor and scale a team of talented Investigators to develop their technical skills and contribute to a high - quality and high performi

akeholders:Clinical Research Associates, Clinical Trial Administrators, Clinical Research Managers, Investigators and relevant site staffRegional CQM, RDQ, Internal/External auditorsTrial Managers, ot

holders.Collectively recommend appropriate mitigation actions and communicate trends to clients and investigators.Provide information on business initiatives in preparation of future fraud investigati

writing of research proposals and, when required, funding proposals. Collaborate closely with other investigators on related studies within the programmes managed by the unit and provide advice or gui

Support of local regulatory and financial compliance.Acquire knowledge how to in/directly influence investigators, external partners and country operations and adheres to budget targets and agreed pay

eholders (internal & external customers, suppliers, shareholders, communities) Internal stakeholders (all divisions) Auditors Law firms and external investigators Internal & External customers

identify further information needed and/or to allocate cases to the appropriate claims specialists/investigators.Document Management Create, organize and maintain files containing the correspondence

ts Manager.Work hand - in - hand with Clinical Trial Administrators, interacting independently with investigators, clinical site staff, vendors, and internal stakeholders.Follows up the contractual pr

as applicable. - Participates in investigator meetings as necessary. May help to identify potential investigators in collaboration with the client company to ensure the acceptability of qualified inve

shes and maintains good working relationships with internal and external stakeholders in particular investigators, trial coordinators and other site staff. May participate in the Health Authority (HA)

identify further information needed and/or to allocate cases to the appropriate claims specialists/investigators.Document ManagementCreate, organize and maintain files containing the correspondence a

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

Detection AdministratorJob PurposeTo register risk events; and provide support services to Forensic Investigators; thereby ensuring that risks are recorded; investigated; actioned and reported in term

s are raised accurately and timeously Appointment of attorneys, contingency agents, loss adjustors, investigators Providing all supporting documentation to attorneys and contingency agents Regular tra

y. Identify potential research gaps and lead/contribute to local post market studies ( contact with investigators, creation and validation of study design, study monitoring, results analysis, etc.). H

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

ists, certified fraud examiners, anti - corruption professionals and money laundering and sanctions investigators. We work with our clients' legal counsel (internal or external) and compliance and int

dings as applicable. Participates in investigator meetings as vital. May help to identify potential investigators in collaboration with the client company to ensure the acceptability of qualified inve

cellent interpersonal and communication skills, with the ability to build strong relationships with investigators and site staff. Problem - Solving: A proactive approach to identifying and resolving i

icle data correction, circumstance scrutiny by applying all relevant checks and provide feedback to Investigators.You Would :Minimizing fraud.Determining the merits of the claimFraudulent versus legit

ocol compliance, data integrity, and patient safety throughout the trial process.Collaborating with investigators and site staff to facilitate smooth study conduct.Performing data review and resolutio

ating procedures and improving team processes.Liaise with attorneys, loss adjusters, assessors, and investigators in ensuring fair outcomes.Manage the relationship between Guardrisk Group and the cell