LogoFresh Jobs Ahead
Precision For Medicine
Precision For Medicine
1,001 – 5,000 Employees
ConsultingHealthcareLogistics
Precision For Medicine is a healthcare and life sciences services organization that helps pharmaceutical and biotechnology companies develop and commercialize therapies, with expertise spanning oncology, rare diseases, and autoimmune conditions. Its work combines clinical trial management, laboratory services, biospecimen collection, biomarker capabilities, and manufacturing support to coordinate complex development programs. By connecting these services across the clinical research process, Precision For Medicine helps teams address operational challenges and advance potential treatments toward patients.
LinkedIn
Company Jobs

Senior Clinical Research Associate – Oncology (Hong Kong, Remote)

Precision For Medicine is seeking a Senior Clinical Research Associate to oversee oncology and global clinical trials in Hong Kong. The role covers site monitoring, regulatory coordination, patient safety, and clinical data quality.

HKHong KongRemoteFull-timeSeniorEnglish RequiredClinical Research
Google Cloud Platform

Description

  • Lead study site management activities that safeguard patients and support reliable clinical data
  • Advise teams on audit readiness, preparation, and follow-up actions
  • Create, monitor, and maintain trial management systems, tools, and status reporting
  • Coordinate site start-up, investigator feasibility and recruitment, EC/IRB submissions, regulatory records, informed consent materials, notifications, translations, and meetings
  • Support study budget negotiations and investigator contract execution as needed
  • Assess informed consent procedures, patient safety, data integrity, protocol deviations, and pharmacovigilance matters
  • Complete pre-study, initiation, routine monitoring, close-out, and oversight visits in line with protocols, local regulations, ICH-GCP, and SOPs
  • Produce monitoring reports, confirmation and follow-up letters, trip reports, communication logs, and related project documentation
  • Contribute to patient recruitment, retention, and awareness initiatives
  • Review, reconcile, and properly archive Investigator Site Files and Trial Master Files
  • Escalate study issues and risks to site staff and Precision project and clinical trial management teams
  • Oversee investigational product inventory, reconciliation, storage, security, dispensing, administration, labeling, importation, and returns
  • Review EDC/CRF records and patient profiles, resolve queries, and address data discrepancies
  • Identify and process Serious Adverse Events in accordance with study procedures
  • Prepare for and participate in investigator, sponsor, global monitoring, and clinical training meetings
  • Contribute to developing protocols, study documents, CRFs, clinical trial reports, presentations, and training materials
  • Coach and train new hires and junior monitors
  • Support client and proposal work, including client presentations
  • Submit investigator payment requests
  • Travel as required by project demands
  • Complete additional responsibilities assigned by management

Requirements

  • Bachelor’s degree or international equivalent, or a comparable combination of education and experience, ideally in business, science, or healthcare
  • At least 3.5 years of on-site monitoring experience
  • Experience working on oncology studies
  • Experience with global clinical trials
  • Advanced proficiency with Microsoft Office, including Outlook, Word, Excel, and PowerPoint
  • Fluent written and spoken English
  • Working knowledge of the drug development process
  • Willingness to travel 60–70%
  • Sustained attention to detail and a high level of accuracy
  • Customer-focused approach with flexibility and a collaborative working style
  • Legal authorization to work in the country of employment without employer sponsorship

Benefits

  • Regular full-time employment
  • Remote work arrangement in Hong Kong
  • Equal Opportunity Employer
  • Reasonable accommodation available for applicants with disabilities
  • Option to opt out of AI use during the application process

Related Jobs

Machina Labs

Director of Defense Business Development, Europe and Middle East

Machina Labs
51 – 200 Employees
ConsultingDefenseLogistics
DEGermanyGBUnited KingdomITItalyNONorwaySESwedenRemoteFull-timeLeadEnglish RequiredBusiness Development Rep

Lead Machina Labs’ defense business development across European markets, expanding opportunities for its software-defined manufacturing factories. Build relationships with defense primes and advance technical engagements into proof-of-concept, qualification, and production programs.

Open
Verisys

Senior AWS Cloud Infrastructure Engineer

Verisys
201 – 500 Employees
USUnited StatesAZArizonaCOColoradoFLFloridaILIllinoisKSKansasKYKentuckyMDMarylandMAMassachusettsMOMissouriNCNorth CarolinaOHOhioOKOklahomaPAPennsylvaniaTNTennesseeUTUtahVAVirginiaWIWisconsin
$145,000 – $155,000 / year
RemoteFull-timeSeniorEnglish RequiredInfrastructure Engineer
AWSCloudDNSEC2LinuxPythonSMTPTCP/IP

Build and secure AWS infrastructure for Verisys’s healthcare credentialing platform. The role spans Linux and Windows systems, Nutanix, containers, certificates, and compliance.

Open