Clinical Research Medical

Samar Al-Saleh

Dubai, United Arab Emirates +971*********, adc17n@r.postjobfree.com

Nationality: Saudi

Profile

Clinical Technologist background and Master of public health degree holder, with ten years experience in clinical research related field.

Diligent, dedicated, organized, thorough and well-ordered professional, with experience with clerical responsibilities in medical organizations.

Practiced in basic statistical tools in research and data analysis, Can use logic and critical thinking to effectively solve problems. An excellent communicator: offering two languages, can communicate confidently and effectively at all levels. A dedicated team member who can work independently and thrives in a team environment to work closely with others. Objective

Seeks opportunities working in Public Health, Biostatistics, Clinical Research and data analysis within an internationally recognized organization that can facilitate further training and professional development within those fields . Education

• DATA SCIENCE Nov 2019 - Feb 2020 Online course Data Mining, Modeling, Tableau and Visualization of large dataset.

• MASTER OF PUBLIC HEALTH NOV 2014 UNIVERSITY OF NEW SOUTH WALES SYDNEY, AUSTRALIA

The program consists of extensive study in topics including health promotion epidemiology, bio-statistics, quantitative and qualitative research methods, health promotion, strategy policy and change services management, tropical disease, outbreak investigation, as well as a systematic review of public health issues

• BACHELOR DEGREE OF CLINICAL LABORATORY SCIENCES DEC 2007 KING SAUD UNIVERSITY RIYADH, KSA

· Major: B.Sc. Clinical laboratory sciences

• ACADEMIC ENGLISH LANGUAGE (OCT 2012 – DEC 2012 UNSW INSTITUTE OF LANGUAGES SYDNEY, Australia

• CLINICAL RESEARCH COORDINATION COURSE MAR 2008- FEB 2009 ACCREDITED BY BARNET UNIVERSITY

RIYADH, KSA

• INTENSIVE ENGLISH LANGUAGE COURSE JULY 2010 THE EDGWARE ACADEMY LONDON, UK

• MICROSOFT OFFICE APPLICATION COURSE 2002 - 2003 NEW HORIZON RIYADH, KSA

Experience

• RESEARCH SPECIALIST – CLINICAL RESEARCH COORDINATOR Al Jalila Children’s Specialty Hospital April 2017- TO DATE

DUBAI, UAE

• Responsible for the coordination and administration of clinical, develop, implement, coordinate research and administrative procedures for the successful management of clinical trials. Performing diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study specific protocols.

• Carrying out data collection and using basic statistical tools in research to draw meaningful interpretation and reporting of the research findings .

• In collaboration with other statisticians and scientists, contribute to analyze data and statistics on living things collected during medical research studies to draw conclusions and execute research studies.

• Writing and implementing Standard Operating Procedure’s for the research department.

• Planning and Leading meeting affectively for research advisory committee members.

• Supervising clinical data collection and analyzing the data for research purposes.

• Sample Processing for clinical trials purposes by performing specimen processing, sample storage, and shipping the samples to the core laboratory as required by the protocol.

• CLINICAL RESEARCH ASSOCIATE MCT-CLINICAL RESEARCH ORGANIZATION NOVEMBER 2015- March 2017

DUBAI, UAE

Participant in the design, implementation and monitoring of clinical trials, preparation of integrated medical reports, INDs, periodic reports, New Drug Applications (NDAs), etc. Participates in design and writing of protocols, case report forms and informed consent forms for clinical trials. Productive in recruitment/selection of new investigators, contract research organizations and outside vendors. Responsible for planning and implementing all activities required to conduct and monitor complex clinical trials and ensures that Good Clinical Practices (GCP) are followed. Conducts site visits pre- study, at study initiation, at regular intervals during the study and at study closeout. Monitors investigator performance and adherence to protocol, and proactively addresses conduct issues and enrollment problems, auditing, source data verification and creating corrective action plans as necessary. Ensures that Case Report Forms (CRF) are reviewed in a timely fashion and submitted to the data management group. Involved in the compilation/writing of integrated medical reports and clinical sections of INDs, New Drug Applications (NDAs) etc. Assists in preparation of presentations and manuscripts of scientific meetings and technical journals. Attends scientific/professional meetings and training courses as appropriate.

• CLINICAL RESEARCH COORDINATOR NATIONAL GUARD HEALTH AFFAIRS DEC 2007- SEP 2012 RIYADH, KSA

• Planning, overseeing and organizing medical research projects at Saudi Arabia’s first BioBank facility.

• Researching and souring viable research subjects. Conducting investigative interviews to collect necessary data. Ensuring consistent accuracy, confidentiality and diligence throughout.

• Representing the center in a public relations capacity, promoting its services and facilities.

• Offering analytical skills and quality control measures to ensure continued excellence across research projects.

• Creating and designing educational medical brochures for the center; providing information to people in an understandable and clear manner.

• Proof-reading, analyzing and editing medical research papers and published articles for medical journals

• Institutional Review Board (IRB) Coordinator: Secondary regulatory resource for investigators and staff for clinical and non- clinical investigations as directed by the IRB Manager. This works in accordance with the processes and procedures that are established by IRB Leadership in accordance with ICH-GCP guidelines.

• Patient enrollment, Database management, Specimen collection, Data Collection, Source document completion and case report form filling (data retrieval)

• Attending meeting, taking minutes of meeting and submit reports that’s serves as an official record.

• LABORATORY TECHNOLOGIST KING KHALID EYE SPECIALIST HOSPITAL JUN 2006 - JUN 2007 RIYADH, KSA

• Based on Phlebotomy and Haematology benches; receiving, processing and analyzing

• Conducting variety of laboratory test services including routinely or experimental processes

• Using, cleaning and maintaining various types of laboratory equipment

• Handling and storing chemicals and related materials

• Carrying out administrative tasks such as maintaining notebooks, documenting procedures,

• RESEARCH ASSISTANT CALGARY LABORATORY SERVICES JAN 2005 - MAR 2005 CALGARY, CANADA

Working as a volunteer based in Immunology Research laboratory. Providing assistance and acting as co-investigator on research paper

(details below)

PUBLISHED PAPERS:

• Influencing factors of knowledge, attitude, and practice regarding antibiotic use in children with upper respiratory tract infections in Dubai

https://onlinelibrary.wiley.com/doi/abs/10.1111/jep.13188

• Knowledge, attitudes, and practice of healthcare workers toward influenza vaccination at Al Jalila Children’s Specialty Hospital (AJCH), Dubai, UAE

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6602923/

• Knowledge and Attitudes Towards AIDS Among Female College of Nursing Students in NGHA, Riyadh, KSA http://sgo.sagepub.com/content/3/3/2158244013499163

• The Prevalence of Cw*0409N Allele and Associated HLA Antigen in Bone Marrow Patients from Alberta http://www.ashi-hla.org/abstracts/2006/view/2384/

ACKNOWLEDGMENT PAPERS:

• Awareness, Attitudes and Practices Related to Swine Influenza Pandemic Among Saudi Public http://www.biomedcentral.com/1471-2334/10/42

• Public Attitude Towards Biomedical Research at Outpatient Clinics of King Abdulaziz Medical Centre – East Mediterranean Health Journal, World Health Organisation http://trove.nla.gov.au/work/153624543?versionld=167419404

• Quality of Informed Consent for Invasive Procedures at King Abdulaziz Medical Centre http://www.ncbi.nlm.nih.gov/pubmed/22505825

• FURTHER PROFESSIONAL DEVELOPMENT:

Attended Workshops at King Abdullah International Medical Research Centre from 2007 – 2012, in the following topics:

• Quality management system (2002)

• Diabetes Care working together for prevention and control (Mar 2002)

• Immunology workshop (May 2003)

• Bio- bank ethics (Feb 2008)

• Therapeutic Updates (Mar 2009)

• Good Clinical Practice Course (Feb 2009)

• Data management and data manipulation using SPSS (Mar 2009)

• Advanced Statistics (Apr 2009)

• Work ethics (Mar 2010)

• Bio-bank ethics workshop (Apr 2010)

• Effective communication (Apr 2010)

• Customer service in healthcare organization (May 2010)

• Tissue bank and its leadership for medical research workshop (May 2010)

• Public health informatics course (Jun 2010)

• Good Clinical Practice (Dec 2010)

• Quality Control.

• Research Methodology.

• Basic Life Support

• Completed one year Internship at Riyadh Medical Hospital from 2005 -2006 in Clinical Laboratory Department.

• Received training in Histocompatibility and Immunogenetics from Calgary Laboratory Services 2005.

• Undertook summer training in Laboratory Departments at Kingdom and King Abdulaziz Medical City in 2004 and 2007- 2012 respectively.

• Declaration of Helsinki (Dec 2015)

• ICH GCP Guidelines (Dec 2015)

• ICH GCP Basic Monitoring Skills (Jan 2016)

• ICH GCP IMP Handling and accountability (Jan 2016)

• Informed Consent Process (Feb 2016)

• Safety Reporting (Feb 2016)

• Fraud and Misconduct (Mar 2016)

• NIH Protecting Human Research Subjects (Mar 2016) OTHER DETAILS

• Languages: Arabic writing and reading (Native); English writing and reading (Fluent)

• Others: Driving license, Qualified in First aid, Computer skills.

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