Detalhes do anúncio |
|||||||||||||||||||||||||
|
Oferta: Senior Clinical Research Associate (FHI Clinical)Tempo Inteiro:Descrição do emprego:
Senior Clinical Research Associate (FHI Clinical)Full-TimeNEW
FHI 360 - FHILogin to Send MessageThe FHI 360 is hiring a Senior Clinical Research Associate (FHI Clinical). Summary of the PositionThe Senior Clinical Research Associate (Sr. CRA) monitors activities at clinical study sites to assure adherence to Good Clinical Practices (GCPs), Standard Operating Procedures (SOPs), study protocols and applicable regulatory requirements. Reviews study documents as required and prepares site visit reports. May be responsible for multiple projects and must work both independently and in a team environment. Participate in the study development and start-up process including reviewing protocols, designing and/or reviewing Case Report Forms (CRF), preparing Informed Consent Forms (ICF's), developing study documents, organizing and presenting at investigator meetings, working with management on a monitoring strategy, and/or developing project-specific CRA training. S/he may participate in clinical training programs and maintain consciousness of developments in the field of clinical research as needed. S/he may provide a benchmark of monitoring competence to inpracticed/less practiced colleagues. Prepares clinical documents, business correspondence, and procedural manuals. Maintain systems and process necessary to report trial status and activities; and to help ensure that quality, regulatory-compliant clinical projects are conducted on time and within budget. Depending upon the level of practice, may become involved, when required, in other areas of study management and staff training and contributes to the review of sponsor/client's and/or FHI360's systems and procedures as appropriate. Responsibilities» Assists in the preparation of routine protocols, informed consent/assent forms, SOPs, and other appropriate study documentation; » Monitors clinical trials to ensure subject safety and compliance with the study protocol, applicable regulations and ICH/GCP Guidelines, may be done with manager; » Coordinates necessary activities required to set-up, monitor, and close-out clinical trials sites; » Conduct site evaluation/assessment, initiation, routine, and close-out monitoring visits may require minimum supervision; » Complete accurate monitoring visit reports; » Develops training materials and conducts training for study implementation located on company policies and SOPs; » Contributes to the development of and implements protocols and informed consents/assents for research studies; » Provides guidance on any protocol-related issues; » Manages budget to ensure CRA activities are completed as per contract; » Develops, reviews, and maintains key study documents to ensure adequate resource and reference documentation; » May serve as a liaison with internal and external partners to ensure effective collaboration efforts; » supervises planning of meetings, site visits, and drafting necessary documents; » Ensures compliance with applicable government regulations when writing and reviewing protocols, analysis plans, reports, and manuscripts; » Provides input with CRF development, analysis, study design, and material management; » Performs and coordinates all aspects of the clinical monitoring and site management process in conformity with ICH Good Clinical Practices, applicable regulations and FHI Clinical SOPs; » Conducts site visits to assess protocol and regulatory compliance and manages required documentation; » Updates and maintains study-specific tracking tools; » May function as project manager on assigned projects taking on a lead function of achieving specific milestone goals to completion; » Responsible for ensuring that data will pass international quality assurance audits; » Represents FHI Clinical in the global clinical research community and develops and maintains collaborative relationships with investigational sites and clients. expertise, expertise and Abilities» May review and approve the work and written reports of team members; » Proven clinical monitoring expertise; » Development and preparation of applicable study tools and documents; » Demonstrates effective management expertise to at least one staff member; » Demonstrates project management capabilities including planning, tracking of milestones/deliverables, and monitoring of resources and budget requirements; Problem Solving and Impact» Works on complex problems that require analysis or interpretation of various factors; » Exercises independent judgement in determining methods and techniques to accomplish results; » Decisions could have a major impact on management and operations of an area within the department; » Determines and develops plans and procedures on new assignments and may direct the work of others. Requirements»suitable education Bachelor’s Degree or its International Equivalent (Education, Health, Behavioral, Life or Social Sciences, International Development, Human Development or Related Field.); »Preferred Job-related practice: Requires 7+ years of clinical research practice including assisting with protocol development, clinical monitoring, study implementation, study closeout, project management, analysis, and reporting. ACRP or SoCRA certification required. Project or technical leadership abilities practice required. Articulate, professional and able to communicate in a clear, positive manner with clients and staff; »Additional Eligibility Appropriate qualifications: Technology to be used: Personal Computer, Microsoft Office (i.e. Word, Excel, PowerPoint, Outlook, SharePoint, etc.), e-mail, telephone, printer, calculator, copier, cell phones, PDAs, and other handheld devices; »Preferences: Must be able to read, write and speak fluent English and French. Advanced degree or its international equivalent preferred. managery or management practice preferred. Global clinical research work preferred; »Physical Expectations: Typical office environment. capability to sit and stand for extended periods of time; capability to lift 5-50 lbs. Travel Requirements» Expected travel time is greater than 25% for this position. How to submit the application:Link: https://shre.ink/IQC Grade: Bachelor, Graduation Employment Type: Full-Time →More jobs at Mozambique →All listings by FHI360 →Explorare vacancies at Associate Anúncios em PortuguêsJob Overview»Date Published: Posted 3 mins ago»Expiration date: June 29, 2022 »Job location: Mozambique »listing title: Senior Clinical Research Associate (FHI Clinical) Apply for job Apply For This JobTo apply for this job please visit shre.ink. Competências:
|
|||||||||||||||||||||||||
Bem-vindo! Registe-se ou Entre na sua conta
December 24 2024
   
|