Clinical Research Assistant

Ramanjot Kaur

**** ******* ***** *, ***** BC Phone : 236-***-****

Vancouver, B.C V4M 4C4 Email: ************@*****.*** Summary

Quality-focused health care professional with 10 plus hands-on experience in clinical research

(Hospital set up as well as CRO cum SMO set up). Talented at developing and actualizing strategies which streamline workflows and improve quality standards. Proven effective at guiding multidisciplinary healthcare teams to succeed in achieving patient outcome goals. Skills

● Training

● Patient Relations

● Comprehensive Problems Solving Abilities

Experience

CIDP India, New Delhi

Assistant Clinical Trials

Manager

06/2021- 02/2022

· Delegated tasks to each member of staff and oversaw task completion, offering assistance to promote success.

· Collaborated with healthcare professionals to deliver high quality patient care.

· Oversaw daily activities and interaction with patients

· Managed clinical operations and procedures and enforced adherence to applicable regulatory requirements

· Interacted with patients, asked appropriate questions and listened carefully to deliver high level of clinical care.

· Coordinated weekly work schedules for department employees.

· Developed and initiated Standard Operating Procedures, policies and other departmental goals.

· Preparation and/or review of any kind of study documents such as protocol, ICD, CRF and any other related documents. Dr. Meena Chhabra's

Medical and Diabetes

Clinic, New Delhi

Research Assistant

(Voluntary)

07/2016-02/2020

· Reviewed new research literature to remain current with examination procedures.

· Used Microsoft Word and Powerpoint to prepare reports, presentations and research results.

· Completed research assignments by organizing data, generating spreadsheets and drafting reports.

· Assisted in research for development of new processes and implementation of usage of new softwares.

· Participated in meetings and other events.

· Met specific confidentiality requirements for all research, data and projects.

· Screened potential subjects to determine suitability for studies.

· Carried out the Informed Consent Process and all trail related activities as per the protocol.

Auriga Research Pvt. Ltd.

Clinical Research

Associate

01/2016-05/2016

· Monitored compliance with applicable guidelines.

· Adhered to standards in areas involving data collection, research protocols and regulatory reporting.

· Collaborated with sponsors and investigators to carry out efficient and fully compliant research trials.

· Preparation and/or review of any kind of study documents.

· Preparation of submission of EC Dossiers.

· Participated in site selection/feasibility and conducted site qualification visits also.

· Conducted site initiation, monitoring and close out visits. Medanta-The Medicity,

Gurugram, Haryana

Clinical Research

Coordinator Group

Lead

11/201*-**-****

· Developed departmental SOPs

· As a team leader trained the CRC's and supervised their work.

· Ensured timely and correct SAE reporting.

· Adhered to standards in areas involving data collection, research protocols and regulatory reporting.

· Obtained informed consent of research subjects or guardians to explain possible side effects and potential outcomes of research.

· Assessed records of each patient, reviewed databases to locate potential research study participants.

· Assisted in collection and processing of specimens from trial participants.

· Managed clinical Trials in multidisciplinary therapeutic areas such as Cardiology, Rheumatology and Oncology.

· Spearheaded all trails from initial visits and meetings (Site Initiation Visits, Monitoring Visits and Site Close out Visits) throughout the completion of trials.

· Prioritize and organized tasks to efficiently accomplish goals. Christian Medical

College, Ludhiana,

Punjab

Clinical Research

Coordinator

07/2010-11/2011

· Adhere to standards in areas involving data collection, research protocols and regulatory reporting.

· Obtained informed consent of research subjects or guardians to explain possible side effects and potential outcomes of research.

· Collaborated with sponsors and investigators to carry out efficient and fully compliant research trials.

· Conducted informed consent presentations and maintained documentation.

· Assessed records of each patient, reviewed databases to locate potential research study participants.

· Kept patient care protocols and clinical trial operations in compliance.

Education and Training

Cranfield University (U.K.) (ICRI Collaborated), New Delhi Master of Science in Clinical Research Sep 2010

Institute of Clinical Research India, New Delhi

Post Graduate Diploma in Clinical Research July 2009 Hans Raj Mahila Mahavidyalaya, Jalandhar, Punjab

Bachelor of science in Biotechnology Vocational June 2008 GCP Certifications

· NIDA Clinical Trials Network 09 Apr 2022

· Good Clinical Practice: A Refresher Course 29 Jun 2021 Conferences and Workshops

· Nursing Research workshop Feb 2014

· HRPP The movement towards and Ethical Research Jun 2013

· Workshop on Clinical Research Ethics Dec 2011

· International Conference on Clinical Research in India Recent Trends, Opportunities & Ways Ahead. Nov 2011

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