Masood Ahmed

**** ********* ******

Norcross, GA 30093

Day Phone: 770-***-****

Immig.Status: Permanent Resident

Email; adir5l@r.postjobfree.com

OBJECTIVE Clinical / Medical Healthcare/ Research, Job (Part time/ Full Time)

EDUCATION

Completed “ACE 6-Day Surgical Skill Lab” For Surgical Assistant

– in Aug.2016

Completed 27 Credit Hrs. In BSN Program from Georgia.

MB.BS, (Equivalent to MD in USA)

BRD Medical College, (University of Gorakhpur),Gorakhpur, INDIA

B.Sc., (Bachelor of Science)

Ewing Christian College, (University of Allahabad), Allahabad, INDIA.

CERTIFICATION

BLS Course for health care providers (CPR & AED) on 04/2013.

Registered Medical Assistant (R.M.A.) from “American Registry of Medical Assistants”. Registration No.111406, Dated; Jan.25,2006

WORK EXPERIENCE

Hearing Aid Outlet Since May/2019 till Sep.8th,2019 5900 Sugarloaf Pkwy, Suite-423, Lawrenceville, GA 30043 Phone; 404-***-**** Worked as Hearing aid Tech (Under Training).

MAGNOLIA MEDICAL CLINIC Since 2009 till 4/24/2018

1235 Indian Trail Norcross, GA 30093

Phone; 770-***-**** Fax; 770-***-****

Worked as Clinical Assistant / Quality Control person

My responsibilities mainly included to;

oAssist physician and physician assistant in exam rooms

oEscort patients to exam rooms, interviews patients, measure vital signs, including weight, blood pressure, pulse, temperature, and document all information in patient's chart

Give instructions to patients as instructed by physician or physician assistant

oTriage and process messages from patients and front office staff to physicians and physician assistants

oEntering all the Patient’s charts in EMR (eCW) regularly.

oAll other duties as assigned by clinical coordinator or practice administrator.

IN-QUEST MEDICAL RESEARCH, LLC 11/01/2010 to 6/21/2011

and 10/2018 to 05/2019

5245 Buford Highway, Peachtree Corners, Georgia 30071,

Phone; 770-***-****

Worked as “Clinical Research Coordinator” in Clinical Research Trials. I worked on

few projects independently which are;

1."Evaluation of Long-Term Safety of PA 32540 in Cardiac patients Who Are at

Risk for developing Aspirin-Associated Gastric Ulcers” from POZEN Company.

2.“Cardiovascular Safety and Efficacy of Febuxostat and Allopurinol" in Patients with

Gout and Cardiovascular Comorbidities” from TAKEDA Company.

My responsibilities mainly included to;

oHaving a working knowledge of protocol and adhering to the sponsor’s protocol specific requirements to meet all study timelines.

oAcquire knowledge of study contacts such as study monitor, study manager and medical monitor.

oAttend sponsor investigator meetings.

oDevelop the source document worksheet (if it is not provided by the sponsor) based on study protocol and EDC system for completion of study data collection.

oObtaining and reviewing the “Informed Consent form (ICF)” from the study subjects and documenting the consent process in the chart.

oScreening and assigning the subject number to study subjects per protocol requirement.

oCompletion and review of all the study specific “Inclusion and Exclusion criteria” and review the source documents to confirm subject’s eligibility prior to randomization into clinical trial.

oRecording vitals and ECG, performing phlebotomy, packing and shipping all the lab specimen.

oWriting notes into the subject’s charts and follow-up on the issues as required for completion of CRF and to meet trial enrollment goals.

oEntering all the data from paper CRF into the electronic data system which included EDC and IVRS.

oPromptly record any potential safety issues or protocol deviations and report them to sponsor and IRB as needed.

oIdentify and resolve the study related issues and queries in EDC in a timely manner and reporting them to the director.

oComplete study subject’s follow-up study visits as required per protocol.

oCompletion of dispensation, collection and return records of all investigational medications.

oComplete and report the AEs and SAEs as required per protocol.

oMaintain an accurate and updated trial screening and enrollment logs.

oComplete the data clarification form (DCFs).

oEnsure the adequate supplies on hand as required to conduct study.

oConfirming that the front office has the accurate information to schedule the subject’s next appointment and compensate subjects for study visits.

oCompletion of all items as outlined in the monitor visit follow-up letter.

oReview regulatory binders to ensure that all documents are in order and up to date.

oContribute to the development of recruitment strategies and study specific enrollment plan.

oWork as an integral team member with respect to patient’s safety, quality and integrity of data and reporting status of study requirement goals and communicate these to the office manager /director.

BEST CLINICAL RESEARCH 03/15/2010 to 10/16/2010

3009 Rainbow Drive, Suit#146, Decatur, GA 30034

Phone; 404-***-**** Fax; 404-***-****

Worked as “Clinical Research Coordinator” in Clinical Research Trials. I worked on

few projects independently which are;

1.“Cardiovascular Safety and Efficacy of Febuxostat and Allopurinol" in Patients with

Gout and Cardiovascular Comorbidities” from TAKEDA Company.

2."Evaluation of Long-Term Safety of PA 32540 in Cardiac patients Who Are at

Risk for developing Aspirin-Associated Gastric Ulcers” from POZEN Company.

My responsibilities included;

oHaving a working knowledge of protocol and adhering to the sponsor’s protocol specific requirements to meet all study timelines.

oAcquire knowledge of study contacts such as study monitor, study manager and medical monitor.

oAttend sponsor investigator meetings.

oDevelop the source document worksheet (if it is not provided by the sponsor) based on study protocol and EDC system for completion of study data collection.

oObtaining and reviewing the “Informed Consent form (ICF)” from the study subjects and documenting the consent process in the chart.

oScreening and assigning the subject number to study subjects per protocol requirement.

oCompletion and review of all the study specific “Inclusion and Exclusion criteria” and review the source documents to confirm subject’s eligibility prior to randomization into clinical trial.

oRecording vitals and ECG.

oWriting notes into the subject’s charts and follow-up on the issues as required for completion of CRF and to meet trial enrollment goals.

oEntering all the data from paper CRF into IVRS system.

oPromptly record any potential safety issues or protocol deviations and report them to sponsor and vice president of the facility.

oIdentify and resolve the study related issues and queries in EDC in a timely manner and reporting them to the director.

oComplete study subject’s follow-up study visits as required per protocol.

oCompletion of dispensation, collection and return records of all investigational medications.

oComplete and report the AEs and SAEs as required per protocol.

oMaintain an accurate and updated trial screening and enrollment logs.

oComplete the data clarification form (DCFs).

oEnsure the adequate supplies on hand as required to conduct study.

oConfirming that the front office has the accurate information to schedule the subject’s next appointment.

oCompletion of all items as outlined in the monitor visit follow-up letter.

oReview regulatory binders to ensure that all documents are in order and up to date.

oWork as an integral team member with respect to patient’s safety, quality and integrity of data and reporting status of study requirement goals and communicate these to the office manager /director.

STUDENT mid 2004 to end of 2006

(In Kaplan test preparation course for USMLE)

In Kaplan Center, Atlanta, GA

Ministry of Health, Saudi Arabia. Nov. 1990 to Nov.2003

RESIDENT DOCTOR

Work assigned: Attending Out patient clinic, looking after in-door Admitted patients in ICU and Wards and first on call for the calls from ER, ICU, and Wards. Participating in teaching and reorientation program for nursing staff.

Ministry of Health, Saudi Arabia. May 1986 to Oct.1990

GENERAL PHYSICIAN In Primary Health Care Centers. Work assigned: In addition to primary medical care I was Involved In Community healthcare along with Health education and survey work for NUTRITIONAL, COMMUNICABLE, CHRONIC DISEASES in several villages.

New-Delhi, India. Jan.1984 to Jan. 1986

Worked as RESIDENT MEDICAL OFFICER (in Private Hospitals)

New-Delhi, India Aug.82 to Jan.84

Worked as JUNIOR RESIDENT in Gen Surgery

Aligarh, India. June 1981 to Jun.1982

Worked as HOUSE OFFICER in Anesthesiology

BRD Medical College, Gorakhpur-India. Feb.1980 to Feb.1981

Completed Compulsory ROTATORY INTERNSHIP TRAINING.

JOB RELATED TRAININGS;

Completed “How to Coordinate Clinical Trials: The Basics”,

CITI (Collaborative Institutional Training Initiative)”Good Clinical Practice Curriculum”- Site Summit Solutions, Basic course passed on 11/26/2010.

CITI “Health Information Privacy and Security (HIPS)” CITI Test Curriculum for Coordinators. Basic course passed on 12/03/2010.

CITI “Human Subjects Research Curriculum”-Site Summit Solution, for Coordinators. Basic course passed on 12/09/2010.

Attended Course on EMERGENCY MEDICINE held on Jan.23- 24th, 2002 at Assir Central Hospital, ABHA, Saudi Arabia..

Attended RESEARCH METHODOLOGY COURSE held at College of Medicine & Medical Sciences, Saudi Arabia, on April-30th, 2001

REFERENCES

Lisa M Crandall, APRN, FNP-BC

Director and Sub-Investigator at In-Quest Medical Research, LLC 5245 Buford Hwy., Suite 106

Peachtree Corners, GA 30071

Phone; 770- 903-0148 / 678-***-****

Email; adir5l@r.postjobfree.com

Gulrukh Mughal, MD

Internist, Northside Hospital Duluth,

3620 Howell Ferry Rd NW, Duluth, GA 30096

Phone; 727-***-****

Email; adir5l@r.postjobfree.com

Shashank Patel, M.D (Internal Medicine and Pulmonary Medicine)

Physician at Magnolia medical clinic,

1235 Indian trail road, Norcross, GA 30093

(On staff at Gwinnett Medical Center and Emory Health System)

Phone; 678-***-****

Email; adir5l@r.postjobfree.com

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