Bikram Kabir, Md Email & Phone Number
Who is Bikram Kabir, Md? Overview
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Bikram Kabir, Md is listed as Senior Medical Director | Drug Safety and Pharmacovigilance at Jazz Pharmaceuticals, a with 799 employees, based in Princeton, New Jersey, United States. AeroLeads shows a matched LinkedIn profile for Bikram Kabir, Md.
Bikram Kabir, Md previously worked as Associate Director | Drug Safety & Pharmacovigilance Physician | Medical Review Safety Expert at Genmab and Medical Review Safety Physician | Clinical Team Member | Liaison (Report Submitting) Health Agencies at Bristol Myers Squibb. Bikram Kabir, Md holds Md, Microbiology from Manipal Academy Of Higher Education.
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About Bikram Kabir, Md
As a trusted Drug Safety and Pharmacovigilance Physician, my goal is to facilitate medical review procedures and proper clinical safety measures across the entire healthcare organization.But my passion for making a difference in the medical community doesn’t begin with where I am today—it starts much earlier when I lost a loved one to leukemia less than a week before starting medical school.It's a big part of helping me become who I am today, and the important role medicine plays in my life today. It sharpens my focus and helps feed my hunger to learn more—driving my collaboration with other team members to achieve better patient outcomes.I am always looking for new answers and solutions through research and am excited by the prospect of using digital transformation to help cutting-edge science achieve even better outcomes for patients in the future.From remote patient monitoring, to data-generated modelling are just a few of the exciting new developments that assist with faster, safer drug development processes that decrease overall cost and enhance patient access.Although the role advanced technology will play in healthcare and wellness is quite promising, it’s also important to remember the role compassion plays in medicine, especially when being separated from the bedside during long periods of research, development and review.Throughout my professional career I have developed a strong work ethic built around positively impacting healthcare by ensuring patient safety during the drug development process, while maintaining a strong sense of compassion for those we are serving.As a physician who understands drug safety, pharmacovigilance and the regulatory requirements of medical review and report submissions—I am excited to see what’s next. With emerging digital technologies real positive impacts can be made through collaboration and establishing meaningful partnerships built on shared knowledge—together.If you would like to learn more about my professional medical drug safety and pharmacovigilance leadership and medical expertise, or how we can work together, I would like to hear from you—please feel free to send me a request to connect.
Bikram Kabir, Md's current company
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Bikram Kabir, Md work experience
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Associate Director | Drug Safety & Pharmacovigilance Physician | Medical Review Safety Expert
CurrentIn my current Associate Director role, I function as the Drug Safety and Pharmacovigilance) Physician for Genmab US Inc, a biotech turned pharmaceutical company that manufactures antibody therapy for patients suffering from cancers and other serious diseases.I was recruited to Genmab as a result of a referral by an ex-colleague and was excited to learn the mid-sized pharma company had launched at least three products with several innovative compounds in the pipeline.As a safety physician on the compound team my primary responsibility is to monitor the overall safety profile of the compound itself. This involves routine medical review and reporting of cases (ICSRs).Most important is the cumulative analysis of these reports—done periodically that provide any emerging signals and/or trends that need immediate intervention or further monitoring.Notable accomplishments:➤Active preparation and participation in regular FDA and EMA filing activities.➤Being part of the “submissions and inspection” team grants access to represent and participate in the inspection, including responding and answering questions (live and written).➤Fostered initiative (currently under implementation) involving the use of Artificial Intelligence (AI) to automate queries helping solicit missing information in patient reports, greatly improving the quality of the queries and the efficiency and effectiveness of site interactions.
Medical Review Safety Physician | Clinical Team Member | Liaison (Report Submitting) Health Agencies
Prior to being recommended for the role I currently hold at Genmab, I was a Medical Review Safety Physician at Bristol Myers Squibb in Princeton, New Jersey. BMS is a publicly traded, multinational pharmaceutical company with annual revenues in the tens of billions.More specifically, my role focused on the review and analysis of adverse event reports and then the submission of said reports to the proper health authorities and governmental officials. This involved the complex medical liaising between clinical team members.During this process, our team discussed significant case reports and partnered with appropriate team members to conduct routine safety surveillance and analysis measures to evaluate the risk/benefit ratio of the compound.Our analysis, oversight and findings were routinely presented in joint functional meetings of which I was an active participant and contributed significant safety data and research.Working for BMS was a significant opportunity to showcase my skills and abilities as a Medical Review Safety Physician for a large multinational pharmaceutical organization. I was able to establish credibility and build trust within the team—leading to better outcomes for patients.
Medical Review Safety Physician | Clinical Team Member | Liaison (Report Submitting) Health Agencies
Before moving to Bristol Myers Squibb (BMS), I held a similar role at Otsuka Pharmaceuticals, a smaller, medium-sized, Japanese-based pharmaceutical company with a primary focus in the area of psychiatry therapeutics.As Medical Review Safety Physician with Otsuka Pharmaceuticals, I again was overseeing and managing the reporting and submissions of adverse advents related to overall drug safety and pharmacovigilance.This included working closely with clinical team members to identify, discuss and elevate significant cases reports—looking for similarities or trends among adverse events that need further investigation.As an active participant in this process, we routinely presented our data, research and findings during regularly schedule function meetings designed to help determine the efficacy of a potential compound—weighing the potential risks and rewards of moving forward.
Medical Review Safety Physician | Member People Engagement Team | Drug Safety & Pharmacovigilance
My tenure as a Medical Review Safety Physician for Accenture was the first opportunity that gave me direct exposure to drug safety and pharmacovigilance.Accenture is a global consulting and outsourcing company with offices all around the world and I was hired to be a Medical Review Safety Physician for one of their practices.In this role, I was able to work as part of the people engagement team which helped form the necessary foundation for the drug safety, medical review and reporting responsibilities I currently perform today.
Manager, Scientific Writing
Manager, Scientific Writing
Colleagues at Jazz Pharmaceuticals
Other employees you can reach at genmab.com. View company contacts for 799 employees →
Marloes Hoff - Van Den Broek
Colleague at Jazz PharmaceuticalsThe Randstad, Netherlands
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Virginia (Ginny) Crooks
Colleague at Jazz PharmaceuticalsNew York City Metropolitan Area, United States
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Cornelia Tolman
Colleague at Jazz PharmaceuticalsThe Randstad, Netherlands
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Jessica Kim, Pharmd
Colleague at Jazz PharmaceuticalsNew York City Metropolitan Area, United States
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Frederik Dahl
Colleague at Jazz PharmaceuticalsCopenhagen, Capital Region Of Denmark, Denmark
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Stefanie Smit
Colleague at Jazz PharmaceuticalsAmsterdam, North Holland, Netherlands
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Lea Costes
Colleague at Jazz PharmaceuticalsNetherlands
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M.Deborah Font Juliá, Md.
Colleague at Jazz PharmaceuticalsThe Randstad, Netherlands
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Mohammed Hussein
Colleague at Jazz PharmaceuticalsCopenhagen, Capital Region Of Denmark, Denmark
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Carly C. Rowland
Colleague at Jazz PharmaceuticalsDenver, Colorado, United States
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Bikram Kabir, Md education
Md, Microbiology
Bachelor Of Medicine, Bachelor Of Surgery (Mbbs), Medicine
Frequently asked questions about Bikram Kabir, Md
Quick answers generated from the profile data available on this page.
What company does Bikram Kabir, Md work for?
Bikram Kabir, Md works for Jazz Pharmaceuticals.
What is Bikram Kabir, Md's role at Jazz Pharmaceuticals?
Bikram Kabir, Md is listed as Senior Medical Director | Drug Safety and Pharmacovigilance at Jazz Pharmaceuticals.
Where is Bikram Kabir, Md based?
Bikram Kabir, Md is based in Princeton, New Jersey, United States while working with Jazz Pharmaceuticals.
What companies has Bikram Kabir, Md worked for?
Bikram Kabir, Md has worked for Jazz Pharmaceuticals, Genmab, Bristol Myers Squibb, Otsuka Pharmaceutical Companies (U.S.), and Accenture.
Who are Bikram Kabir, Md's colleagues at Jazz Pharmaceuticals?
Bikram Kabir, Md's colleagues at Jazz Pharmaceuticals include Marloes Hoff - Van Den Broek, Virginia (Ginny) Crooks, Cornelia Tolman, Jessica Kim, Pharmd, and Frederik Dahl.
How can I contact Bikram Kabir, Md?
You can use AeroLeads to view verified contact signals for Bikram Kabir, Md at Jazz Pharmaceuticals, including work email, phone, and LinkedIn data when available.
What schools did Bikram Kabir, Md attend?
Bikram Kabir, Md holds Md, Microbiology from Manipal Academy Of Higher Education.
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