Jana Nathan, Ccrc, Ccrp, Csm Email & Phone Number

Mississauga, Ontario, Canada

Ontario, Canada

Ontario, Canada

Canada

Toronto, Canada Area

Toronto, Canada Area

Acted as a consultant/expert resource to guide, advise, educate and train CRCs to maintain high standards of quality across LMC sitesDeveloped and maintained templates/resources to guide research staffs in the conduct of clinical research to facilitate regulatory complianceConducted routine and random QA audit across the sites to ensure compliance to SOPs, ICH-GCP and ProtocolDeveloped and disseminated new policies/CAPAs in response to emergent issues impacting quality/riskGuided CRCs with SIV, trial conduct and final close out visits Collaborated with the QC team for quality improvement, SOP revision and company-initiated goalsPromoted and educated research team on regulations, guidelines and best practices to conduct research

Toronto, Ontario, Canada

Conduct Early and Late phase Clinical research studies in accordance with Study Protocol, GCP, and the LMC Research SOPResponsible for recruiting, informed consent procedures, screening, study coordination and study completion of multiple early and late phase studiesMonitor, record and report all AEs and SAEs to the Investigator, sponsor and IRB as requiredTrain Investigators and study staffs on protocol and IC amendmentsAssist QA department with audit preparation and quarterly review for CRCs

Scarborough

PHARMA MEDICA RESEARCH INC Screening Medical Data Reviewer (Quality Control)Ensure that all screening files for each study are accurate and legible according to the study protocol and relevant SOPs.Ensure accurate preparation of screening Case Report Forms (CRFs).Review study files set up for recruiting and subjects screening file in subject database.Review of other study related documentation, protocols.Provide report on the reviewed data to the supervisor of the study and follow-up upon resolution.Inform Screening Coordinator related issues and give suggestions for the accuracy and quality of data.Interact with other departments to improve the accuracy and quality of data.Perform other assigned duties as directed by Director, Subject Selection or designate.Assist in SOP revisionEnsure proper documentation of clinical activities according to SOP, GCP, Health Canada, FDA or other regulatory agency guidelines.Participate regularly in all training program and evaluations in all PMRI training including SOP, GCP testing and PMRI in-home training modules. Ensure Health and Safety rules and regulations are adhered at all times.

Toronto, On

Maintain recruiting accuracy of qualified candidates to meet protocol requirementsCapture medication and medical history of study participants and document in CESRPrepare, check and update screening files accurately and ensure legibility according to study protocolExperienced in auditing clinical study protocolComplete clinical activities according to GCP, SOP guidelines and ETD/TPD regulationFollow Joint Health and Safety rules and regulations at all timeVerify subject identification and document screening packages as a screening receptionistParticipate in training programs including GCP, SOP training and PMRI in-house training modulesPreserve subject confidentiality and minimized risk in keeping with Privacy and Confidentiality Policies and Procedures, as well as other applicable organizational/program guidelines

Active Brain Center

•Create an optimal learning environment and engage kinesthetic, visual and auditory learners through mental arithmetic and brain training exercises for the implementation of programs specially designed to encourage whole brain development among children

Sunnybrook Health Science Center

Contribute, as part of a team, to helping patients improve the quality of their lifePrioritize, organize and prepare patients for their medical appointments with specialists/ oncologists while ensuring their comfortWeigh and record patient weight in an accurate mannerOrganize and prepare patient files for the oncologist, including tracking and locating missing filesAssist in other areas, adapting readily to changing demands to ensure operational efficiency

Clinical Research Associate Certification, Clinical Research

Communication skills and the use of technology to effect the communication Ethical theory and ethical issues related to clinical research.

Human Biology Specialist Bsc., Biology

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