Work from home Clinical research Jobs

Navitas Life Sciences hiring Senior Clinical Research Associate (SCRA) in Thailand & Work from home option is available

cNavitas Life Sciences. Thailand (Remote)

Senior Research Associate -(SCRA)

Functional superior: Sr./Clinical Project Manager-Clinical Deveopment Operations

Responsibilities and functions:

Working in accordance with ICH E6 principles and with applicable SOPS (either Navitas Life Sciences or

Sponsor’s SOPs) & local regulatory norms.

Accompanied visit as a part of mentoring a new CRA

Conduct of Feasibility assessments

Project set up activities:

Conduct of site selection activities Negotiation & facilitating Investigator/site contract
execution Development & local adaption of study specific documentation
Set up of the trial master file

Project conduct
Maintenance of TMF
Facilitating Regulatory submission

Prepare, conduct & participate in Investigator’s
meeting

Conduct Site initiation and site monitoring

Remote Monitoring, Central Monitoring and Risk Based Monitoring related activties

Maintain communication with study teams at site Maintain communication with clients and vendors as back-up for a project manager/project team lead based on the requirements

Resolution of site level issues & where necessary escalation of issues to PM
Support PM/PTL with project updates

Participate in client meetings/teleconferences interdepartmental meetings

Support in vendor selection, agreement and
co-ordinatiion

CRF retrieval & Query turnaround

Facilitate site payments

Registration Link check below

Navitas Life Sciences hiring Senior Clinical Research Associate (SCRA) in Thailand & Work from home option is availablecNavitas Life Sciences. Thailand (Remote)Senior Research Associate -(SCRA)Functional superior: Sr./Clinical Project Manager-Clinical Deveopment OperationsResponsibilities and functions:Working in accordance with ICH E6 principles and with applicable SOPS (either Navitas Life Sciences orSponsor's SOPs) & local regulatory norms.Accompanied visit as a part of mentoring a new CRAConduct of Feasibility assessmentsProject set up activities:Conduct of site selection activities Negotiation & facilitating Investigator/site contract
executionDevelopment & local adaption of study specific
documentation
Set up of the trial master fileProject conduct
Maintenance of TMF
Facilitating Regulatory submissionPrepare, conduct & participate in Investigator's
meetingConduct Site initiation and site monitoringRemote Monitoring, Central Monitoring and Risk Based Monitoring related activtiesMaintain communication with study teams at siteMaintain communication with clients and vendors as back-up for a project manager/project team lead based on the requirementsResolution of site level issues & where necessary escalation of issues to PM
Support PM/PTL with project updatesParticipate in client meetings/teleconferences interdepartmental meetingsSupport in vendor selection, agreement and
co-ordinatiionCRF retrieval & Query turnaroundFacilitate site paymentsRegistration Link check below
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