Malek Najjar, Phd Email & Phone Number

Texas, United States

Houston, Texas, United States

Houston, Texas

Describes the biological function of gene products, the effect of genomic variants and the association with disease, using clinical vocabularies, ontologies and established guidelines. Works with genetic couplers and laboratory directors on single- gene experimentation and high throughput genetic testing. Provide accurate classification on genetic variants.

Pine Brook, New Jersey

• Direct new assay development. Design and validate amplicon based cancer panels on ion torrent platform for oncology (myeloid, lymphoid and solid tumor) and genetic testing (BRCA1/2, hereditary cancer) in CLIA- and.
• Variant interpretation and classification for NGS testing based on professional guidelines, literature and database search.
• Prepare clinical reports of actionable variants detected in NGS tests according to indications, panels ordered and other available clinical information.
• Create and maintain an in-house databases of clinically actionable variants.
• Validate operating system and bioinformatics software upgrade.
• Participate in new molecular test development, which include planning validations, assay design, data compilation and documentation of regulatory submission. Compose validation summaries with relevant description of.

Waltham, MA

• Oversaw and monitored activities of assigned investigative sites and clinical trial projects throughout the clinical study, ensuring high quality execution of clinical studies, safety, adherence and compliance to.
• Conducted on-site monitoring visits at investigators sites, including pre-study, site initiation, routine ongoing and close-out activity visits. Ensure that site protocol deviation and Serious Adverse Events (SAEs).
• Developed and maintained relationship with Principal Investigators (PIs) and research staff by arranging for WebEx teleconferences and preparing and sending out newsletters to provide the necessarily training.
• Served as back-up project manager and involved in planning and managing all aspects of clinical trial, including financial aspects of clinical study such as reviewing invoices, performing daily account tasks, preparing.
• Participated in collaboration with multidisciplinary submission team in writing and reviewing NIH-FDA Clinical Trial Protocol for a medical device to treat postoperative Acute Kidney Injury (AKI). Provided variety of.

Boston, MA

□ Pharmacology and Experimental Therapeutics, Sackler School of Biomedical Sciences.□ Over the course of PhD study, extensive classes in Biochemistry, Pharmacology and Biostatistics were taken. Being in Pharmacology program allowed students to attend postgraduate courses in clinical pharmacology, drug development and regulation in addition to the weekly.

Tucson, AZ

• Primary direct care provider for patients undergoing dialysis treatment. Won best employee in the clinic several times.
• Calibrated readings on instruments according to standards. Decreased rate of failure machine to the minimum.
• Prepared hemodialysis machines to be ready for patients. Put patients on dialysis machine in timely manner without affecting safety of patients.
• Provided hemodialysis care to patients under the direction of the nephrologist. Understood nephrologists order and were help to the charge nurses in dialysis clinic.
• Performed medical laboratory tests to provide data for diagnosis and dialysis efficiency for patients.
• Provided assistance to about 15 junior-level staff and mentored with general dialysis tasks, as directed by nephrologists and according to standard dialysis procedures.

Tucson, Arizona Area

Primary direct care provider for patients undergoing dialysis treatment

Doctor Of Philosophy (Phd), Pharmacology And Experimental Therapeutics, 3.78

Postgraduate Course In Clinical Pharmacology, Drug Development And Regulation

Clinical pharmacology, drug development, clinical trials, and regulation.

Doctor Of Medicine (Md), Medicine