Clinical Research Manager

TFSHealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full-service capabilities, resourcing, and Functional Service Provider (FSP) solutions.
JoinOurTeamasaClinicalResearchManager(CRM) - home based in Poland, Spain or Italy.
AtTFSHealthScience,youwillbepartofaglobalteamdedicatedtoadvancinginnovativetherapiesandimprovingpatientoutcomes.WearelookingforanexperiencedClinicalResearchManager(CRM)tojoinourOphthalmologyteamandplayakeyroleinoverseeingclinicaltrialoperationsacrossmultiplestudiesandcountries.

Thisisafull-time,home-basedopportunityopentocandidateslocatedinPoland,Spain,orItaly

Aboutthisrole

AspartofourOphthalmologyteam,youwillworkalongsidepassionateandinnovativeprofessionalstoensureourcustomersachievetheirclinicaldevelopmentgoals.

TheClinicalResearchManager(CRM)willberesponsibleforcoordinatingandoverseeingcountryandsitemanagementactivitiesduringstudyconductincompliancewithcompanypolicies,SOPs,ICH-GCPguidelines,regulatoryrequirements,andcontractualobligations.

YouwillworkcloselywithProjectManagers,ClinicalResearchAssociates(CRAs),sponsors,andinvestigativesitestoensurestudiesaredeliveredontime,withinscope,andtothehighestqualitystandards.

KeyResponsibilities

Manageday-to-dayclinicaloperationsactivitiesforassignedprojectsinaccordancewithstudyprotocols,contracts,SOPs,ICH-GCPguidelines,andapplicableregulations.

Serveastheprimarysponsorcontactforoperationalproject-specificissuesandstudydeliverables.

Lead,coach,andsupportCRAs,ensuringproject-specifictrainingrequirementsarecompletedanddocumented.

Overseesitequalityandmonitoringdeliverablesthroughdirectsupervisionandguidanceofstudyteams.

Developandimplementstudymonitoringplans,sitetrainingplans,andverificationinitiatives.

Coordinateinvestigatormeetingsandsupportsiteandcountry-levelstudyreportingactivities.

Ensurestudyprocessesandoperationalstrategiesremainpracticalandeffectivefromfeasibilitythroughstudycloseout.

ActastheprimarypointofcontactforCRAsandmonitoringteams,providingguidanceonsite-relatedchallengesandescalations.

Supportrecruitmentandmonitoringstrategiestooptimizestudyperformance.

Conductco-monitoringvisitstoensurequalityoversightandconsistencyacrossmonitoringactivities.

Reviewandapprovemonitoringvisitreports,ensuringtimelyresolutionandescalationofidentifiedissues.

Reviewmonitoringschedulesandsitevisitcalendarstoensurecompliancewithmonitoringplans.

Monitorprotocoldeviations,datalistings,andqualitymetricstoproactivelyidentifyrisksandimplementmitigationstrategies.

LeadstudyteammeetingsandprovideregularupdatestoProjectManagersregardingsiteandcountryperformance.

EnsureaccuratemaintenanceofstudydocumentationandTrialMasterFile(TMF)quality,whendelegated.

ReviewCTMSdatatoensuretimelyandaccuraterecordingofcountry,site,andsubjectinformation.

Supportinvestigatorpaymenttrackingandapprovalprocesseswhendelegated.

CollaboratewithProjectManagersonCRAonboarding,training,andhandoveractivities.

Contributetostudycommunications,newsletters,andoperationalupdates.

Provideprojectinsightsrelatedtoresourceutilization,revenuerecognition,andforecastingactivities.

ParticipateinInvestigatorMeetingsandpresentmonitoringrequirementsandexpectationswhenrequired.

Promoteproactiveissueresolutionandasolution-orientedapproachacrossstudyteams.

PartnerwithCRALineManagersregardingstudyassignments,workloadplanning,andperformancediscussions.

Supportbusinessdevelopmentinitiatives,proposals,budgetdevelopment,andbiddefenseactivitiesasrequired.

Qualifications

Bachelor'sdegreeinLifeSciences,ClinicalResearch,Nursing,Pharmacy,oranotherhealth-relatedfield.

Minimumof5yearsofclinicalresearchexperience,includingsignificantexperienceasaClinicalResearchAssociate(CRA)withindependenton-sitemonitoringresponsibilities.

Minimum 1 year experience as an Unmasked CRA / CRM in an Ophthalmology study.

Experiencecoordinatingoroverseeingclinicaltrialoperationsatastudy,country,orregionallevel.

Strongunderstandingofclinicaltrialprocessesfromstart-upthroughcloseout.

In-depthknowledgeofGoodClinicalPractice(ICH-GCP),regulatoryrequirements,andclinicalresearchstandards.

For candidates based inItaly

Salary: €63,000 – €65,000 gross/year, in line with CCNL Terziario-Servizi (Level III), plus benefits (lunch vouchers, health insurance, pension, and car allowance where applicable).

We welcome applications from candidates belonging to protected categories under art. 1 L. 68/99.

WhatWeOffer

Weprovideacompetitivecompensationpackage,comprehensivebenefits,andtheopportunityforpersonalandprofessionalgrowthinarewardingenvironment.You'llbejoiningateamthatvaluescollaboration,innovation,andmakingadifferenceinthelivesofpatients.

AtTFSHealthScience,you'llhavetheopportunitytoworkondiverseandimpactfulclinicaldevelopmentprogramswhilecollaboratingwithtalentedcolleaguesacrosstheglobe.

ABitMoreAboutUs
Ourjourneybeganover25yearsagoinSweden,inthecityofLund.AsaglobalCROwiththeultimategoalofensuringpatients'safetyandwell-being,weprovidebiotechnologyandpharmaceuticalcompanieswithtailoredclinicaldevelopmentsolutions.Wecurrentlyoperatein17countriesacrossEurope,NorthAmerica,AsiaPacific,andtheMiddleEast.
OurcorevaluesofTrust,Quality,Flexibility,andPassionarewhatmakeTFSHealthSciencethesuccessfulcompanyitistoday.Thesevaluesshapeourculture,reflectwhatwestandfor,andguidehowweworkeveryday.

#TogetherWeMakeADifference

Originally posted on Himalayas