Project Manager (Clinical Trials)

Skip to ContentServicesAboutOur Specialization StrategyDrug SafetyRegulatoryIND PreparationClinical StrategyProject ManagementBiostatistics & ProgrammingSite MonitoringData ManagementMedical WritingClinical ExpertiseAreas of ExpertiseOncologyRespiratoryEndocrinologyRadiopharmaceuticalsAboutOur TeamOur PhilosophyOur LocationOur CapabilitiesCareersCertified Diverse BusinessContact UsServicesAboutOur Specialization StrategyDrug SafetyRegulatoryIND PreparationClinical StrategyProject ManagementBiostatistics & ProgrammingSite MonitoringData ManagementMedical WritingClinical ExpertiseAreas of ExpertiseOncologyRespiratoryEndocrinologyRadiopharmaceuticalsAboutOur TeamOur PhilosophyOur LocationOur CapabilitiesCareersCertified Diverse BusinessContact UsFolder: ServicesBackAboutOur Specialization StrategyDrug SafetyRegulatoryIND PreparationClinical StrategyProject ManagementBiostatistics & ProgrammingSite MonitoringData ManagementMedical WritingFolder: Clinical ExpertiseBackAreas of ExpertiseOncologyRespiratoryEndocrinologyRadiopharmaceuticalsFolder: AboutBackOur TeamOur PhilosophyOur LocationOur CapabilitiesCareersCertified Diverse BusinessContact UsProject Manager (Clinical Trials)Project Manager (Clinical Trials)Position: Full TimeLocation: RemoteJobDuties:• Evaluate and train investigators• Attend investigator meetings• Conduct pre-study initiation visits• Orient site personnel to study protocol and procedures• Perform on-site and remote monitoring activities from study start-up through close-out• Verify accurate transcription of data from source documentation to CRF/EDC• Oversee drug accountability• Ensure regulatory inspection readiness at assigned clinical sites• Perform all duties and responsibilities in adherence to protocols, FDA regulations, ICH/GCP guidelines, and company / client SOPs• Minimal travel may be required, based on study specifications• Perform other related duties as neededKnowledge & Skills:• Extensive knowledge of FDA regulations and GCPs• Computer proficient with EDC experience• Detail oriented• Excellent verbal and written communication skills• Ability to work independently with minimal supervision• Ability to proactively identify issues that may impact enrollment and recruitment timelinesEducation andExperience:• BS/BA in Life Science or Nursing (or equivalent foreign education / experience) required• Minimum of 3 years CRA experience within the pharmaceutical or biotechnology industry• This position can be contract, full-time, or part-time.To apply, send resume and cover letter to [email protected] with subject line "Project Manager". ContactEmail : [email protected] : + 1 (215) 623-9900Corporate642 Newtown Yardley RoadSuite 200Newtown, PA, 18940, USA Apply tot his job