Clinical Research Associate
Employment Information
Report this job
Job expired or something wrong with this job?
Job Description
Clinical Research Associate monitoring oncology and dermatology clinical trials for global CRO TFS HealthScience. Ensuring participant safety, data integrity, regulatory compliance, and accurate study-site documentation.
Responsibilities:
- Function operationally as a member of a Project Team
- Initiate, monitor on-site and remotely, and close out study sites during study conduct
- Monitor clinical trials according to company and sponsor SOPs, GCP, ICH guidelines, and applicable regulations
- Perform monitoring activities to assess subject safety, data integrity, and quality
- Verify informed consent procedures and protocol compliance
- Review electronic or paper CRFs and subject source documentation for validity and accuracy
- Verify management and accountability of investigational product
- Prepare Monitoring Visit Reports, document findings and corrective/preventive actions, update tracking systems, and escalate issues
- Provide sites with identified issues and required action items
- Deliver site documents to eTMF or paper TMF and verify Investigator Site File maintenance
- Participate in audit or inspection preparation and follow-up activities
- Order, ship, and reconcile clinical investigative supplies when applicable
- Update CTMS and other project systems with accurate site-level information
Requirements:
- Bachelor’s Degree, preferably in life science or nursing; or equivalent
- Over 1 year of relevant clinical experience or relevant academic background around clinical trial or clinical development activities
- Ability to work in a fast-paced environment with changing priorities
- Basic medical terminology and science associated with assigned drugs and therapeutic areas
- Understanding of Good Clinical Practice regulations and ICH guidelines
- Ability to work independently and in a team matrix organization
- Strong written and verbal communication skills
- Fluent in English and German
- Excellent organizational skills
- Technology savvy with good software and computer skills
- Ability and willingness to travel up to 60-80%, including overnight and abroad travel if applicable
Benefits:
- Competitive compensation package
- Comprehensive benefits
- Opportunity for personal and professional growth
- Collaborative and innovative work environment
- Opportunity to make a difference in the lives of patients
Similar Jobs
Clinical Trial Manager
Clinical Trial Manager managing timelines, quality, vendors, and stakeholders for ICON’s sponsor-dedicated clinical research programs. Supporting trials that advance patient treatments.
Clinical Research Associate II
Clinical Research Associate II monitoring Phase 1–4 clinical trials for AbbVie, a medicines and healthcare solutions company. Ensuring site compliance, data quality, safety reporting, and regulatory readiness.
Clinical Monitor, Clinical Research Associate, CRA
Clinical Research Associate monitoring German clinical trials for ClinSol’s contract research programs. Coordinating sites, regulatory submissions, study data, and investigator communication.
Clinical Research Associate
Clinical Research Associate monitoring sponsor-dedicated clinical trials for ICON Strategic Solutions. Ensuring protocol compliance, data integrity, and patient safety across Greek study sites.
Clinical Trial Manager
Clinical Trial Manager overseeing sponsor-dedicated clinical trials for ICON Strategic Solutions. Managing protocols, stakeholders, compliance, vendors, and study delivery.
Senior Clinical Research Associate
Senior Clinical Research Associate overseeing clinical trial monitoring, site management, and recruitment for Alimentiv. Home-based in Portugal with regular travel to sites in Portugal and Spain.
Principal Biostatistician, FSP
Principal Biostatistician leading clinical-trial design, analysis, and regulatory support for Cytel’s pharmaceutical clients. Applying advanced statistics, R, SAS, and simulation methods across Phase I-IV studies.
Clinical Research Associate II/Senior – Oncology
Clinical Research Associate monitoring oncology trials for Thermo Fisher Scientific. Ensuring site compliance, data quality, essential documentation and audit readiness through frequent field visits.
Clinical Research Associate II
Clinical Research Associate II advancing AbbVie’s clinical trials for innovative medicines. Monitoring investigative sites, ensuring compliance, data integrity, patient safety, and recruitment performance.
Clinical Data Manager
Clinical Data Manager overseeing clinical trial data quality, EDC builds, and database lock activities. Supporting Telix Pharmaceuticals’ precision radiopharmaceuticals for cancer and rare diseases.
Clinical Research Development Analyst
Clinical Research Development Analyst supporting clinical trial strategies, protocols, and regulatory dossiers. Contributing to new medicine approvals and clinical data generation at Libbs Farmacêutica.
Early Clinical Scientist – Translational Medicine
Early Clinical Scientist coordinating early-phase clinical trials for Parexel’s clinical development services. Overseeing safety, data validity, CRO performance, and trial documentation.
Clinical Trial Manager, Class III Medical Devices
Clinical Trial Manager coordinating Class III implantable-device trials at Biogen, a biotechnology company. Managing sites, vendors, compliance, risks, and regulatory workflows.
Clinical Research Lead
Clinical Research Lead managing investigators, sites, enrollment, and vendor oversight for ICON’s sponsor-dedicated clinical research programs in the UK.
Clinical Research Associate II
Clinical Research Associate II monitoring oncology clinical trials for PSI, a contract research organization. Managing site visits, data integrity, regulatory documents, and investigator communications.
Clinical Research Site Manager, Neurology
Clinical Research Site Manager overseeing startup, enrollment, compliance, and performance across neurology clinical-trial sites for Johns Hopkins University. Remote role based in the Baltimore, Maryland area.
Biostatistician, Neurology
Biostatistician analyzing longitudinal neurology data for Johns Hopkins School of Medicine. Developing SAS/R analyses, datasets, statistical plans, and publication-ready results.
Senior Clinical Research Associate
Senior Clinical Research Associate monitoring clinical trials for Precision for Medicine, a specialized clinical research organization. Coordinating study setup, site visits, regulatory compliance, client support, and junior staff mentoring.
Senior Clinical Research Associate
Senior Clinical Research Associate monitoring clinical trials for Precision for Medicine, a specialized CRO. Ensuring protocol compliance, site oversight, and sponsor collaboration across Spain.
Senior Clinical Research Associate
Senior Clinical Research Associate monitoring clinical trials for Precision for Medicine, a specialized CRO. Coordinating study setup, site monitoring, regulatory activities, clients, and junior CRA mentoring.