Training Clinical Research

MOHAMMAD BILAL

A-**/* Abul Fazal Enclave, Okhla, New Delhi-110025

CELL: +91-839********, +91-874*******

E-MAIL: *******************@*****.***

SUMMARY

A professional offering 6 months of experience in research coordination of clinical studies. Demonstrated ability to support the management and coordinate the tasks of multiple research studies. Expert in liaising between different departments. Special talent for creating and maintaining databases and reports.

AREAS OF EXPERTISE

Research Coordinator SAE Compensation and reporting ICMR Guidelines

Study data collection DCGI Guidelines Drug Study

Data Analysis and study IRB/EC Meetings GCP Guidelines

Medical Device Study Detailed Documentation Data Capture Enhancement

WORK EXPERIENCE

FORTIS ESCORTS HEART INSTITUTE

(Fortis Healthcare is a pioneer in the field of fully dedicated cardiac care facilities in India).

DEPARTMENT OF ACADEMICS AND RESEARCH (SIDCER RECOGNISED)

From JENUARY 2018 Research Coordinator /Assistant

Initiate, manage and monitor research projects and provide project specific administrative support.

Conducting independent study coordinating and screening potential patients for protocol eligibility.

Data Collection and follow up visits of patient.

Study gathered data to determine accuracy for trails. Review medical records to ensure completeness and accuracy.

Summarize research findings and make appropriate presentations.

Coordinating Ethics Committee meetings and performing review and analysis of submitted sponsored projects and other projects.

Liaising between medical professionals and help in understanding projects and thesis submitted by performing thorough review.

Reduce-IT: “A Multi-Centre, Prospective, Randomized, Double –Blind, Placebo-Controlled, and Parallel-Group Study to Evaluate the Effect of AMR101on Cardiovascular Health and Mortality Hypertriglyceridemic Patients with Cardiovascular Disease or at High Risk for Cardiovascular Disease”.

SPNC-ELCA-1016 Study : A Prospective, Open label, Non-randomized, Single-Arm, Multicenter Study to Evaluate the Procedural Safety and Efficacy of ELCA® in Treatment of Patients with Single or Multivessel Coronary artery disease (CAD).

MyVal-1: A prospective, metacentric, single arm, open label study of MyVal Transcatheter Aortic Valve Replacement System in the treatment of severe symptomatic native aortic valve stenosis.

Manage and solve the entire study related query, documentation, follow up with the subjects enrolled into the study.

Maintenance of each subject files and look for completeness for the subject records/documents as per visits.

Contact point for patients/sponsors local colleagues for trial related activities

IRB/EC meetings.

Communicate with DCGI regarding SAE’s occurred in study.

DISSERATION/TRAININGS

1 Month Training at Sun Pharmaceutical Industries, Majeedia Hospital, Hamdard Nagar and Auriga Research Private Limited, Kirti Nagar, New Delhi

1 April 2017- 28 April 2017

Training regarding BA/BE studies, Data management, Protocol writing and Documentation

GCP certified by NIDA Clinical Trials Network

1 Month Project on Prevention and Treatment of Tuberculosis at Hakim Ajmal Khan Memorial Hospital, Rampur-2015.

I start my dissertation on 1st Jan 2018 Fortis Escort Heart Institute.

Since 1st Jen-2018 I work as Clinical Research Coordinator in Fortis Escort Heart Institute, Okhla New Delhi. And also doing here my Thesis project.

Attend GCP training program at Meri Life Sciences Pvt. Ltd, Vapi Gujrat.

Attend ICTD on 19-May-2018 at Medanta Hospital, Medicity, Gurugram, Haryana.

Training Regarding ICD- Components and ICF process by Dr. Nandini K. Kumar

Former Deputy Director General Senior Grade (ICMR) at Fortis Escorts Heart Institute (08-Jun-18)

PROFFESIONAL SKILLS:

Trained in Good Clinical Practices and regulatory guidelines (ICH guidelines )

Experience of Regulatory practices concerned with DCGI and Ethics Committee work such as proofreading studies before initiated and record findings if any then scrutinize scientific validity and feasibility of the study under the guidance of PI.

Acquired sound knowledge of Ethics Committee/ Ethical Guidelines.

Acquired hands on experience in data management, Drug handling and maintaining trial related records/data.

Experienced with site Standard Operating Procedure and practices.

PESONAL SKILLS

Highly motivated and dedicated to my work.

Open to new learning opportunities and experiences.

Enthusiastic and positive.

Good communication skills and interpersonal skills.

EDUCATION

Jamia Hamdard University, New Delhi

2016 to present

Master of Science in Clinical Research

Mahatma Jyotiba Phule Rohilkhand University

2013-2016

Bachelor of Science –Chemistry and Zoology

Saraswati Vidhya Mandir, Rampur, Uttar Pradesh

2013

Senior secondary

Saraswati Vidhya Mandir, Rampur, Uttar Pradesh

2011

Secondary

TECHNICAL SKILLS

1.Good at Word Document, Power point And MS Excel

EXTRACURRICULAR

Attend ICH-GCP training in MERIL ACADEMY at Vapi Gujrat.

NABH training in Fortis Escort Heart Institute.

I hereby declare that all the above said facts are true to my knowledge.

Date: 28/06/18

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