Mohammed

With a robust background as a clinical research specialist, I bring a wealth of hands-on experience to the table, ensuring tasks are completed accurately within set deadlines. My firm grasp of medical terminology and unwavering dedication to confidentiality underpin my ability to provide precise, timely documentation that aids healthcare professionals in delivering top-notch care. My expertise in documentation is enhanced by exceptional communication skills, facilitating my smooth integration into medical teams.

I am fervently dedicated to continuous professional development, keeping abreast of the latest industry advancements to uphold the utmost standards of accuracy and efficiency in all clinical research endeavors.

Clinical Operations Manager - AL MANDOOB MEDICAL CARE SERVICES - Abu Dhabi

(2021-01)

Physician Assistant/Clinical Trial Specialist - CITIZENS HOSPITALS - Hyderabad

(2014-01 - 2020-12)

Coordinator - CARE HOSPITALS, BANJARA HILLS - Hyderabad

(2008-01 - 2013-12)

Job Profile: Job Involves Assisting the consultant into various aspects clinical as well as in the administrative areas.

• Updating the in-patient status
• Following the clinical rounds with the Consultant
• Take medical histories, perform physical examination, treat patients, order and interpret diagnostic procedures and record the data in Out-patient Chart
• Following the rounds of Inpatient care setting, develop and implement patient management plans and record progress notes
• Instruct and counsel patients regarding compliance with prescribed therapeutic regimens health maintenance and disease prevention
• Facilitate referral of patients to other medical or surgical specialties when appropriate
• Admissions, discharges, and out-patient pt care
• Format the discharge summaries
• Assist the Physician in various Research Trials and Medical Audits
• Medical statistics of the ongoing research programs
• Interpreting the various diagnostic procedures
• Collaborated with cross-functional teams to align project objectives and business goals

Coordinator - CARE FOUNDATION, INSTITUTE OF CARDIAC RESEARCH AND EDUCATION - Hyderabad

(2008-01 - 2013-12)

Responsibilities as a Coordinator

• Provide subject care and data collection procedures in adherence with the assigned study protocol and in accordance with good clinical research principals
• Recruitment and co-ordination of trial subjects covering informed consent, screening and visit coordination
• Ensure that IRB approval of protocol and informed consent form is obtained prior to initiation of the study
• Performs other study related tasks as assigned by Principal Investigator & CRO
• Review subject charts, database records, and other sources to screen and identify potential subjects for inclusion in study based on criteria described in the protocol
• Confer with subject and physician to explain purpose of study. Coordinate to obtain written consent for subject to participate in a study prior to initiation of any protocol procedures
• Maintain accurate records of the receipt, inventory, and dispensation of study drug and materials
• Obtain and coordinate subject blood samples, cultures, tissues, and other specimens for laboratory analysis as described in study protocol
• eCRF filling (Inform, Mednet, Oracle base Data management)
• Case Record Form filling
• Serious Adverse Event Reporting to the IRB and Sponsor
• Communicates with the sites on administrative matters such as Ethics Committee communication and site agreements and payments
• Well versed in using the IVRS system for studies

Post Graduate Diploma in Physician Assistant (PGPA) - Physician Assistant - CARE FOUNDATION, INSTITUTE OF CARDIAC RESEARCH AND EDUCATION

Master of Science (M.Sc) - SUJATHA POST GRADUATE COLLEGE, HYDERABAD

Bachelor of Science (B.Sc) - OSMANIA UNIVERSITY