Mahetab Negm’s CV 4 pages
Address: POB: 511, Riyadh, Postal code 11421
Tel:
Email:
+966-566250525
Maahetab.negm82@gmail.com,
N_toby82@yahoo.com ,
Negmma@ngha.med.sa,

Developing a long term Career in Research.
Communication skills
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Excellent communication, follow up and documentation with the IRBs, sponsors and their representatives, colleagues and Principal investigators.
Teamwork and Leadership skills
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Responsible for training newly hired employees either as a pharmacist or as a research coordinator.
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Handled several research projects.
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Inpatient In-charge pharmacist.
Time management skills
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Able to meet extreme deadlines and work under severe work condition.
Computer Skills
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Excellent handling of
1.
Microsoft Integrated Package
2.
Micromedex, WIPRO, KFH1, Cort-tex, Quadramed Health care systems.
3.
Oracle and other eCRF systems.
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Bachelor Degree in Pharmaceutical Sciences, Mansoura University-Egypt (2004-2005).

International General Certificate of Secondary Education-The British Council-Riyadh.

Manarat El-Riyadh Schools-Riyadh. (International Section).
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Mahetab Negm’s CV
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Project Management Professional Expected
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SOCRA Certification for Clinical Research Professionals
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ACRP Certification for Clinical Research Associates
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ACRP Certification for Clinical Research Coordinators
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IATA training for Transport of Hazardous Elements (Category B).
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Project Management Professional Exam preparation Course
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CITI online training program for IRB members
 Quintiles’ GCP online training
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11th Clinical Research Professional's Course-KFSH&RC-Riyadh.
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OHPR training for protection of human subjects

1 st
aid training
4 pages
Feb 2015
Sep 2014
Sep 2014
Sep 2013
Oct 2010
Nov 2014
Oct 2012
Feb 2011
Nov 2009
Nov 2009
2005

January 2013-Now: Clinical Research Coordinator at King Abdullah International
Medical Research Center-Ministry of National Guard- Health Affairs a.
Implementing, commenting and revising new protocols/protocol amendments/ appendices,
CRFs, informed consents, questionnaires, study budgets, agreements before submission to the IRB. b.
Preparing and attending (as a CRC for our site and as CRA for other sub sites) feasibility initiation/ monitoring/ close out visits/ Assuring appropriate filling of TMF. c.
Following up with patients / sponsor representatives / sub sites. d.
CRF and eCRF completion / Verification for sub sites /chart reviews e.
Processing, collecting and reporting AE within the timeline frames. f.
Screening patients for eligibility g.
Implementing new recruitment strategies/ Consenting patients.
Research activities:
Project manager and Co-I in a multicenter observational study in the ER settings.
Phase IV hepatobiliary, Ob-Gyn and Oncology studies.
Clinical Trial Unit Assistance
(Responsible for reviewing protocols before submission to the IRB) .
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Mahetab Negm’s CV 4 pages
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October 2012-January 2013: Clinical Research Specialist at King Fahd Medical City a.
Implementing and commenting on new protocols/protocol amendments b.
Preparing and attending site visits initiation/monitoring/close out. c.
Following up with patients / sponsor representatives d.
CRF and eCRF completion /chart reviews Data abstraction / Database updating. e.
Processing, collecting and reporting AE within the timeline frames f.
Assuring appropriate filling of TMF g.
Screening and consenting patients / implementing new recruitment strategies.
Research activities:

Responsible for all Comprehensive Cancer Care Centre Clinical trials
Phase II, III and IV Nasopharynx, Head and Neck, and Colon Oncology Clinical trials
Reason for leaving: Failure of Sponsorship transfer
June 2012 –September 2012: Clinical Research Coordinator in Clinserv International a.
Implementing and commenting on protocol amendments b.
Preparing and attending site visits initiation/monitoring/close out/ Assuring filling of TMF c.
Following up with patients/ site. d.
Processing, collecting and reporting AE within the timeline frames e.
CRF and eCRF completion / chart reviews / Data abstraction/ Database updating. f.
Screening and consenting patients / implementing new recruitment strategies
Research activity: A phase III Clinical trial in genetics in KFSH&RC
Reason for leaving: Failure of Sponsorship transfer
 December 2011-May 2012: Clinical Research Coordinator in Ministry of National
Guard- Health Affairs a.
Patient recruitment/ chart review. CRF completion.
Research activity: An observational study in the ER settings
Reason for leaving: End of Study (Project based hiring)
 April 2011 to December 2011: Clinical Research Coordinator in King Faisal Specialist
Hospital and Research Center.
a.
Administering and explaining informed consents. b.
Patient recruitment/ chart review. c.
Following up with patients/ sponsor. d.
CRF completion/ processing and collecting of Questionnaires.(Ob-Gyn Oncology)
Research activity: An epidemiological study in OB-Gyn oncology
Reason for leaving: End of Study (Project based hiring)
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Mahetab Negm’s CV 4 pages
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March 2010 to March 2011: Clinical Research Coordinator at the Oncology
Department-Ministry of National Guard – Health Affairs a.
Implementing, commenting and revising new protocols/protocol amendment, their appendices, CRFs, informed consents, questionnaires, study budgets, agreements before submission to the IRB. b.
Preparing and attending (as a CRC for our site and as CRA for other sub sites) feasibility initiation/ monitoring/ close out visits/ Assuring appropriate filling of TMF. c.
Following up with patients / sponsor representatives / sub sites. d.
CRF and eCRF completion / Verification for sub sites /chart reviews e.
Processing, collecting and reporting AE within the timeline frames.
Research activity:
Phase II, III and IV Lung, Breast, Colon and Pancreatic Oncology Multisite Clinical trials.
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September 2008 to October 2009: Pharmacist in Al-Hammadi Hospital a.
Reviewing physician’s orders with patient profiles to ensure proper dispensing of pharmaceuticals. b.
Identifying and correcting potential allergic reactions, drug interactions and incompatibilities. c.
Preparing, checking and dispensing of medications and preparations. d.
Preparing various instruction guides including I) List of oral dosage forms that shouldn't be crushed, II)Refrigerated items in the hospital with their therapeutic indications, III)
Pediatric doses of antihistamines ,cough syrups, and nasal decongestants, IV) High alert medications in the hospital and their safety measures. e.
Taking part in the updating of formulary 2009-2010. f.
Taking part in safety of drugs in pregnancy and lactation project. g.
Participating in patient and pharmacist education programs.
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May 2006 to May 2007 : Pharmacist in Motherhood and Infancy Centre a.
Reviewing physician’s orders with patient profiles to ensure proper dispensing of pharmaceuticals. b.
Identifying and correcting potential allergic reactions, drug interactions and incompatibilities.
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