Shanshan Lan Ph.D., M.D., Ccrp Email & Phone Number

Montreal, Quebec, Canada

Montreal, Quebec, Canada

• Regulatory affair expertise in clinical research protocol Research Ethic Board (REB/IRB) Reviewer |CIUSSS of Montreal | Montreal, QC, Canada
• Expertise in regulatory submission by reviewing clinical trial protocols, participating in REB/IRB meetings, presenting 1-2 clinical research protocols, reviewing over 5 clinical research protocols each month.

Montreal, Quebec, Canada

• On-site Clinical Research Monitoring Experience Clinical Research Associate |Jewish General Hospital | Montreal, QC, Canada
• Ability of on-site coordinating and monitoring Covid-19 Biobank Study (BQC19), with more than 1800 patients enrolled. Participated in McGill University Bio-portal study (Endocrinology) start-up, compose and modify ICF.
• An expert of productivity enhancer and make patient recruitment effective, by filtering 10 high-priority patients for recruitment, over 100 patients recruited within first three months, productivity increased by 20%..
• Ability to monitor project. Check consistence of protocols, SOPs, ICF, CRF, sample record monthly, and maintain and managing study documents, preparing for annual REB/IRB audit, to run the clinical study smoothly.

Montreal, Quebec, Canada

• Reviewed scientific literature in Nephrology to support knowledge background.
• Presented research data using graphics and statistical software at academic conferences.
• Cross-functional collaboration with physicians, scientist, and health professionals.
• Perform research project on Renal Transplantation.

Montreal, Quebec, Canada

• Filled-in CRF, IND/ FDA form 1571, CTA form, Informed Consent, AE/SAE reports, ConMed verification, Data SDV
• Prepared/verified documents for phase II/III Metabolic Syndrome and LDL-C studies
• Verified initial submission to IRB, Informed Consent Form
• Adapting CRF and ICF to study protocol
• Performed Data Entry of raw laboratory data from the above studies in the CRF template
• Performed data entry with Datatrack e-CRF/CTMS

Changchun, Jilin, China

• Clinical research monitor and managementClinical Research Physician (Dermatologist)|First Hospital of Jilin University|China
• Project management ability and expertise of collaborating with healthcare professionals, lead three clinical trials and assisting 7 clinical trials (pembrolizumab, dupilumab, tky2 inhibitor, Jak inhibitor, IL17/IL23.
• Ability of presenting scientific data and concept, as Interpreted clinical data and presented in national and international scientific conferences.

Changchun, Jilin, China

Technical transfer skill by performing flow cytometry diagnosis for 5-10 clinical leukemia patient and Rt-PCR respiratory virus infection test daily.

Ph.D, Biomedical Sciences

Activities and Societies: •2015.09: Canadian Donation and Transplant Research Program (CDTRP) trainee, Canada Ph.D. Biomedical Science.

Master'S Degree, Medicine, Plastic Surgery, Master

Plastic surgery training • Thesis: Isolation and differentiation of human primary adipose-derived stem cells.

Doctor Of Medicine - Md, Clinical Medicine

Clinical Reseach Professional

Activities and Societies: Systematic Approach to Effectively Manage Multi-Center Trials, • IND & CTA, IRB, SSU, TMF, CRF, AE/SAE, SDV.