• Job Target: Drug Safety
• Employment Status: Employed - Actively Looking
• Experience Level: Mid Level
• Seeking: Full-Time
• Industry: Management Resumes

• Salary:
• Degree: Doctorate (PhD/MD/JD)
• Security Clearance: Confidential (Level I)
• Travel: Moderate
• Relocate:: No

Objective

Luljeta Istrefi MD
4100 Stevens Road Apt 4123, Wallington, NJ 07057
Cell: 973-851-0011
Email: luljetaistrefi@yahoo.com

Career Objective:

Seeking the position of a drug safety associate with a view to utilize my interest, credentials and work experience in the field of medical towards professional growth and development

Core Competencies:

Comprehensive knowledge of international drug safety and pharma co-vigilance principles and regulations
Extensive knowledge of drug safety and drug development process and procedures
In-depth knowledge of coding principles, submission criteria, regulatory time line requirements, technical requirements and guidelines
Possess sound communication skills both in verbal and written
Familiar with basic computer and database applications
Good leadership, analytical, problem solving and time management skills
Significant intercultural and international experience, including fluency in English, Albanian, Croatian.
Professional Experience:

Organization: Dendrite.

Duration: October 2004 till September 2009.
Designation: Medical Information Specialist

Handle responsibilities of reviewing and processing adverse events reported by investigators
Perform the tasks of conducting research and analyzing medical and scientific literature
Responsible for providing medical and scientific information to health care professionals
Perform the tasks of reviewing bio equivalence study protocols, clinical trial protocols, and provide support the clinical trial team
Handle responsibilities of developing concise, accurate and well-written case narratives
Perform the tasks of maintaining the safety database and perform coding of diseases as well as adverse events according to the project-specific coding conventions
Responsible for making presentation of safety process at clients and investigator meetings and Regularly meet with MIC Director to share product information.
Organization: Medi Media
Duration: April 2008 to December 2009
Designation: Physician advice

Medical Consultant providing study-related data to pharmaceutical company clinical practitioner involved in various drug research studies.
Handle responsibilities for Adverse Event reports during discussions with physician or pharmaceutical professionals.
Perform the tasks of checking patient eligibility for clinical trials
Handle responsibilities of entering data into the database and reporting systems
Perform the tasks of assisting comprehensive reviews of serious-adverse events
Responsible for drafting case narratives and processing case-related information
Educational Summary:

Medical Doctor Degree –February 1998

University of Medical & Dentistry of Pristine.

Achieved Master's degree in Public Health.
University of Medical School in Pristine.

Job Target

Drug Safety

Education

Skills

• Medical Doctor