...better access to treatment.
Every day, we rise to the challenge to make a difference and here’s how the Pharmacovigilance (Senior Manager) Senior Safety Medical Reviewer role will make an impact:
The Senior Medical Reviewer will be responsible to assist in the global...
...TCS is hiring for Pharmacovigilance professionals!
Skill - Pharmacovigilance
Work Location - Pune
Experience Range - 1 to 7 Years... ...local procedural documents and local implementation of Patient Safety objectives, policies, processes, and procedures.
*Responsible...
...Bangalore, is a department within the Clinical Drug Development area. It is a perfect blend of skilled medical professionals (Medical reviewers) and technical programmers (Functional... ...with a focus on ensuring overall patient safety and wellbeing of all clinical trial participants...
...Medical Reviewer, ICSR
at ClinChoice (View all jobs)
Bengaluru or Hyderabad - India... ...current knowledge of product portfolio and safety profiles for products across... ...manage as appropriate.
Maintain Pharmacovigilance expertise and understanding of international...
...TCS is hiring for PV Drug Safety!
Role: Pharmacovigilance
Work location: Mumbai
Experience: 1 - 7 years’ relevant experience in Pharmacovigilance
Qualification: Bpharm/ Mpharm/ BHMS/ BAMS/ BDS/ Msc (Biotechnology, Zoology)
Job Description:
*Ability to...
...Drug Safety Physician (DSPs)
Job duties of a Drug Safety Physician include:
Reviewing and analyzing adverse event reports, clinical trial data, and other safety information... ...authorities
Preferred Qualifications
A medical degree (MD or DO)
Experience in drug...
...position is a member of Global Patient Safety – Pharmacovigilance Compliance and Safety Operations -PV... ...areas as well as vendor resources to review and implement medium to complex change... ...disabilities globally. If, because of a medical condition or disability, you need a reasonable...
...Wipro Kolkata is hiring for Drug Safety Physician.
Work Location - Kolkata
qualification... ...or MBBS/MD degree from recognized Indian Medical College / Foreign Graduate Students must... ...Experience – 2 Yrs to 4yrs in PV as Medical reviewer
Immediate joiners are preferred....
...Department : Global Safety GBS (GS - GBS).
Does your motivation... ...The Position
A Senior Drug Safety Associate will perform initial... ...required.
~ Sound knowledge of Pharmacovigilance is expected.
~ Knowledge of medical terminologies and clinical pharmacology...
...business requirements or for company/team events.
Responsibilities
Evaluate manuscripts posters slide decks educational material medical literature provided by clients for data accuracy
Check documents (mentioned above) developed by medical writers for scientific...
...Responsibilities for pharmacovigilance scientist
- Act as core member for... ...Ensure timely, quality reports/safety analyses related to core... ...information, etc), contribute and review Informed Consent Forms (ICF),... ...of the clinical trial medical team, represent PVRM in SAE reconciliation...
...Responsibilities for Global Patient Safety (GPS) Medical Review1.Medical support of individual... ...staff in ensuring appropriate follow-up, reviewing assessments providing review for the... ...European Union Qualified Person for Pharmacovigilance (QPPV)
Ensure support is provided...
...Job Description
Medical reviewers at Analyst/Senior Analyst level review or audit the medical records for completeness and accuracy by looking... ...and insurance guidelines. They should have basic knowledge on drugs medical devices common medical treatment procedures at Primary...
...research solutions, quality compliance, pharmacovigilance, medical information, and RD technology,... ...accelerate our partners most high-profile drug and device programs.
Job Summary... ...Responsible for case processing or quality review of coding all medical history, events,...
...collaboration with the Global Program Safety Lead (GPSL) provides robust... ...evaluation expertise and medical innovation in order to... ...activities such as literature review, evaluation of individual cases... ...activities as required by providing pharmacovigilance inputs to initial development...
...be the partner of choice in drug development.
Roles & Responsibilities... ...and programs, and the main pharmacovigilance point of contact for assigned... ...own service area through review of project specific plans and... ...such as but not limited to Safety Management Plans (SMP) or SAE...
...be the partner of choice in drug development.
That’s our vision... ...line listings and applicable safety information to clients,... ...quality and compliance metric review, finance tracking and oversight... ...Maintenance of project information or Pharmacovigilance intelligence information with...
Remote job
...Central Report Reviewer
Syneos Health® is a leading fully integrated... ...translate unique clinical, medical affairs and commercial... ...defined, with a focus on patient safety, protocol/GCP/regulatory compliance... ...Sponsor’s requirements and pharmacovigilance issues documented in the...
...to be the partner of choice in drug development.
That’s our... ...Roles & responsibilities:
• Review and process serious adverse events... ...reactions and/or other medically related information per assigned... ...Provide input and review relevant safety tracking systems for accuracy...
Remote job
...the role
This role combines responsibilities in Medical Safety Operations (addressing pharmacovigilance (PV) needs) with broad Project Management activities... ...supported processes (and IT systems) by way of regular reviews to identify gaps / issues and/or improvement needs (...
...Job Title: Medical Content Reviewer
Location: Hyderabad Telangana
Job Type: Fulltime (onsite)
Job Overview:
We are seeking an experienced and detailoriented Medical Content Reviewer with minimum 56 years of clinical experience to join our dynamic medical content...
...Pharmacovigilance Associate Responsibilities:
Process and manage adverse event reports: This includes reviewing AE reports from healthcare professionals, patients, and other sources. They... ...to regulatory authorities.
Maintain safety databases: Pharmacovigilance Associates...
...About this Job:
Are you passionate about medical academics and teaching Do you have excellent written communication skills Can you... ...Office) then we have an exciting opportunity for you as a Medical Reviewer.
The Medical Reviewer is responsible for ensuring...
...Conduct and execute all pharmacovigilance related activities in Unichem... ...PV team to prepare periodic safety update reports (PSURs) and submitting... ...timely manner.
Work with medical, scientific, clinical and... ...marketplace.
Mentor in writing review article, case study and post...
...customer success. We translate unique clinical, medical affairs and commercial insights into... ...SAS programming background – Medical and Safety Data Analytics Preferred. SAS programming... ...worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 2...
...Pharmacovigilance Associate- Freshers
Essential Duties and Responsibilities
Collect and evaluate adverse event reports from various sources, including healthcare professionals, patients, and drug company representatives
Assess the severity and causality of adverse...
...In short, to be the partner of choice in drug development.
That’s our vision. We’re driven... ...to the pharmaceutical, biotechnology and medical device industries. This individual will... ...documentation, preparing periodic reports and reviews of certain cases, identify potential...
Remote job
...position typically refers to any employee within the EPD Medical organization with medical /scientific qualifications and... ...Medical Advisors; Medical Information team / specialists; EPD Pharmacovigilance / drug safety personnel
•Marketing department across therapeutic...
...coordination and delivery of safety writing services for multiple... ...activities within a highly regulated pharmacovigilance environment driven by strict... ...: project management data review authoring and quality review.... ...reports; Periodic Adverse Drug Experience Reports (PADERs))....
...solutions drive job opportunities and satisfaction for all stakeholders.
Role Description
This is a full-time on-site role for a Pharmacovigilance Trainer. The Pharmacovigilance Trainer will be responsible for developing and delivering training programs on pharmacovigilance...