Usman Ghani Resume Clinical Research

1. USMAN GHANI (M.D)
9467 w Longview pkwy Kansas City, MO 64138
913-523-5414 (cell)
usmanghani1984@aol.com
Willing to relocate. Nearest airport MCI 38 mins away.
OBJECTIVE
Dependable and hard-working foreign country CRA-MD is seeking CRA position.
Highly motivated team player, with excellent organizational, interpersonal, verbal and
writing communication skills.
Strong attention to detail, functioning well under work demand, prioritizing and
recognizing timely work requirements.
Strongly interested in conducting research in an ethical and safe manner.
PROFESSIONAL EXPERIENCE
 Study Coordinator: PSCHIATRY ASSOCIATE OF KANSAS CITY
(PAKC)2017-2018
 EHRHARDT CLINICAL RESEARCH, BELTON, MO 2017
Performed duties of Study Coordinator in conducting 4 research studies of CNS
therapeutic areas, i.e. PPD, Depression, Tourette syndrome, TMS.
Entering patient records in EHR system, helped Sub-I and PI to develop Research center
in Kansas City region.
Developing ICF, and source documentation according to protocol, patient screening, I/E
criteria, labs collection and processing, phlebotomy, audit reports, patient visits, EDC
Data entry and query resolution, IRB submission and follow up, AE and SAE recording
and SAE submission to IRB, IMP accountability and re-ordering, communication with
Sponsor, CRO, and vendors.
CRA EXPIRIENCE:
Rx Pharmaceutical, LTD, Lahore, Pakistan-2010-2014
Therapeutic Areas:
Oncology, solid tumors-Phase II-III
Oncology liquid tumors-Phase III
Hepatitis-C-Phase III
Endocrinology/Diabetes mellitus Type II
GI-Gastro-enterology- Phase II
Cardio-vascular Phase III

2. Respiratory-Asthma and Allergy-Phase III
CNS/Depression, PPD-II-III
Responsibilities:
As a field CRA conducted all 4 different visits, i.e. Site Selection Visits-SSV, Site
initiation Visit-SIV, Routine Monitoring Visits-IMV, and Closing Visits-COV. In
addition, conducted multiple SWAT SSVs and co-monitoring visits
Responsibilities included but not limited to: Identifying and selecting sites for
participation, training site personnel on protocol during SIV, and re-training upon
necessity, conducting monitoring visit with 360 degrees data verification between source
documents and CRF, both paper and electronic, remote monitoring via EDC, queries
resolutions, working with study coordinators and PIs for clean and accurate data
submission, performing drug accountability as blinded monitor, monitoring SAEs and
assure timely submission to IRB, identified deviations to protocol and work with sites to
their resolutions, working with Data Management during data clean up, preparing sites
for Sponsor Audit, writing Confirmation letters, reports and follow up letters after each
visit, identifying site weak enrollment and performance issues, and supporting them for
successful improvement, review regulatory documents preferably during each IMV when
possible, work with sites to improve enrollment and retention numbers, submitting
documents to TMF, attending Investigator Meeting.
Timely completed required SOPs and training courses.
QUALIFICATION S
Highly motivated, dedicated, and detail-oriented professional with over 10 years of
healthcare experience including patient management at both in and out-patient facilities
and years of experience in conducting clinical research under PI/Sub-I supervision.
Driven by new challenges and desire to be successful, offers superior communication,
leadership, management and organization skills.
PROFESSIONAL STRENGTHS
ICH GCP
FDA REGULATION
IRBs
Data collection and processing, attention to detail
Clinical trials. Phase(s) II-III
Large group presentation
Team management
Superior communication skills
Cross-functions working capabilities
Great learning abilities
Medical terminology expert
US CERTIFICATION

3.  NIH (National Institute of Health) Current
 GCP (NIDA clinical trials) Current
EDUCATION
CLINICAL RESEARCH FASTRACK AZ, USA 2017, CRA
FRONTIER MEDICAL SCHOOL, Abbottabad, Pakistan
 Bachelor of Medicine and Bachelor of Surgery, 2010 GPA:3.24
 Conducting and assisting in Researchduring the years in Medical school.
PERSONAL ATTRIBUTES
Detail-oriented, timeline driven, good listener, eager and fast learner.
Excellent communication and client/vendor service skills.
Perform and travel well under tight and demanded schedule.
Perform well as an individual and team player, always keeping satisfactory goal
completion in mind.
Analytical and respectful, work well in multicultural settings.
SKILLS
EHR System, EDC, EMR
 Microsoft Word, Microsoft Outlook
 Microsoft Excel
 Microsoft PowerPoint, Skype.
REFERENCES
Status: US Permanent Resident.
All Diplomas and Certificates are translated and evaluated in USA by WES, and
available upon request.
Professional references:
 CJ Anderson (president at FINDING PHARMA) -Mentor (480)-355-5278.
 Lauren Ballina - CCRC, NATIONAL DIRECTOR OF CLINICAL RESEARCH
FASTRACK AZ Instructor-Mentor (724)-575-2342
 Jody Ehrhardt (CEO EHRHARDT CLINICAL RESEARCH BELTON, MO)
Supervisor (816)-405-6076
 Dr Sherman Cole MD (913)-385-7252
 Dr Dennis P. Owens MD (913)-385-7252
Personal Reference:
Vita Gredinberg, Sr. CRA-408-410-7876

4. Personal interests: Quality time with family and friends, outdoors, listening to classical
music, meditation. Non- smoking.