Management Data

Riaz Bandali

**** ********** ***** **** *****: 250-***-****

Victoria, British Columbia, V8P 1Z1 E-mail:

********@****.**

EMPLOYMENT HISTORY

Clinical Research Coordinator (Level 1)

Pharmaceutical Research Associates (PRA) International, Victoria, BC

February 2011 – Present

Develop, implement, validate, review and/or maintain data management plans, study documents, case

report form modules and other related documents and guidelines in accordance with individual study

protocols. Responsible for clinical database, data entry screens and data validation programs. Ensure that

project deliverables are achieved in terms of timelines, quality and budget. Troubleshoot and propose

solutions to study design, process and technical issues. Provide constructive study feedback to peers, Lead

Clinical Data Coordinator (LCDC) and functional management. Demonstrate effective and diplomatic

communication strategies in internal team meetings, client meetings and project report and status update

meetings with management. These include queries to investigational sites, query resolution with

investigational sites and/or Clinical Research Associates and relaying of information to LCDC and

functional managements with regard to quality or process issues that may impact the study. Follow PRA

and client Standard Operating Procedures.

Sales Associate (Merchandise Expediting Team)

Home Depot Canada, Langford & Saanich locations, BC

October 2009 – February 2011

Operated and oversaw new employee training on forklifts, saws and other machines and tools used at

Home Depot. Worked with vendors and management to collectively agree on how to set up (planogram)

each merchandise bay. Qualified industrial first aid attendant and provided treatment as needed.

Presented seminars to the public on diverse “how to” projects.

Dive Instructor

Ogden Point Dive Centre, Victoria, BC

May 2006 – Present (satellite instructor)

Achieved PADI Open Water Dive Instructor certification through PADI Americas in 2006. Fully insured

and qualified for instruction in open water, advanced open water, rescue diver, dive master and additional

specialty courses.

CLINICAL TRIALS EXPERIENCE

• Oncology: Neuroendocrine Tumors – Phase III trial

• Neurology: Traumatic Brain Injury – Phase III trial

• Gastroenterology: Colorectal Cancer – Phase II trial

• Respirology: Moderate/Severe Asthma – Phase IIIB trial

• Rheumatology: Gout – Phase III trial

EDUCATION

• Clinical Research Associate Diploma (Honours), Clinical Research Training Centre, Montreal, QC,

March 2013

• Nursing (incomplete), Camosun College, Victoria, BC, September 2005 – June 2007

• Biochemistry (BSc), University of Victoria, Victoria, BC, April 2005

APPLICABLE KNOWLEDGE & SKILLS

• Certified in Oracle Clinical Database Software

• Certified & fluent in Datalabs and JReview programs

• Experience and expertise with Clinical Data Management systems and relational database

management systems.

• Able to achieve high quality and accurate clinical data by ensuring all identifiers are accurate and

developing edit checks and query specifications.

• Able to perform all aspects of data management tasks from clinical trial preparation to close-out

of study utilizing paper and/or electronic format.

• Experience in using relational databases as well as experience using Clinical Data Management

and Electronic Data Capture products

• Able to provide necessary training to clinical associates & able to guide teams on data capture

methods.

• Capable of preparing Case Report Form design including the development of requirements,

specifications, designs, annotations, and training materials for CRFs, utilizing paper and electronic

formats.

• Able to provide written specifications and procedures for loading non-CRF data into the database

in collaboration with data analysts.

• Able to ensure that user acceptance testing is completed prior to implementation and deployment

to clinical trial sites and ensure that the requirements for data transfers and integration with other

systems are defined.

• Able to oversee the review of incoming CRF’s and DCF’s (Data Clarification Form) for

completeness, consistency and clarity. Managing and tracking CRF flow, including scanning as

required. Enter and update data as needed.

• Able to collaborate with database analysts and CRAs in the requirements, specification, design,

development, testing, and documentation of Clinical Trial databases.

• Experience in coding processes as they relate to project needs

• Able to represent Clinical Data Management on the Clinical project team.

PROFESSIONAL AFFILIATIONS

ACRP Association of Clinical Research Professionals (Member)

SCDM Society for Clinical Data Management (Member)

PADI Dive Association (Member)

REFERENCES

Available upon request.

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