...Pharmacovigilance Associate Responsibilities:
Process and manage adverse event reports: This includes reviewing AE reports from healthcare professionals, patients, and other sources. They need to assess the seriousness of the event and determine whether it needs to be...
...complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality compliance, pharmacovigilance, medical information, and RD technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de...
...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...
...and accurately.
• Serve as Functional Lead on case processing or medical information projects as assigned; coordinates teams of Pharmacovigilance associates on project level and serves as the Pharmacovigilance point of contact for project teams.
• Effectively maintains...
Remote job
...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...
...Responsibilities for pharmacovigilance scientist
- Act as core member for assigned products
- Ensure timely, quality reports/safety analyses... ...preparation of aggregate safety reports for newly launched Novartis products to meet regulatory requirements
- Alert the Medical...
...Role & responsibilities
Conduct and execute all pharmacovigilance related activities in Unichem lab.
Train PV Team, corporate office, manufacturing plants and other vendors as applicable in timely manner.
Ensure preparation and maintenance of pharmacovigilance...
...education, outreach and 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...
...Director of Professional Services Pharmacovigilance
LocationNoida
Experience 15 to 20 years
Must have
Experience in Pharma CoVigilance.(Minimum 5 Years)
Experience in a leadership role
Experience in Jira
Experience in project management
Experience in...
...Position : MICC Executive (Pharmacovigilance)
Experience : 0-3 Years
Qualification : M. Pharm /B. Pharm/ B.sc/ M.sc
Location : Gota Ahmedabad
Salary - Up to 4 Lacs
JD:
- Receive and process assigned voicemails
- Update the Voicemail Tracker
- Receive information...
...Company Description
We are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider initially established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and...
...Identify, track and resolve Protocol Deviations (PDs) as per Novartis processes. Detect potential PDs based on regular clinical data... ...experience in Clinical Data Management,
relevant experience in Pharmacovigilance
relevant experience in Clinical Project Management....
...innovation in order to improve patients’ lives and impact on overall Novartis results. As a member of the Medical Safety organization,... ...Safety Lead in submission activities as required by providing pharmacovigilance inputs to initial development and updates of core data sheet (...
...scientific inputs at study and program level, thereby supporting Novartis in reimagining medicine for patients worldwide.”
Your... ...documents for study CSR activities, and publications.
• May support pharmacovigilance activities (e.g., reviewing/contributing to aggregate reports/...
...include, but are not limited to:
1. Efficiently manage contracted pharmacovigilance services outsourced to ESP covering all operational aspects (... ...audit compliance with closure of finding (if any), alert Novartis management of pending compliance issues, audit findings at partner...
...About the role
Millions! Novartis made a decision to pursue early discovery research internally to allow us to quickly translate... ...patients. With the ever-evolving global regulations in the field of pharmacovigilance, with a focus on pragmatic approaches to protecting patient...
...Global QA (e.g. medical risk assessments for escalations) and Pharmacovigilance (e.g. RMP/pregnancy prevention program/plan, DHPC); Technical... ...career opportunities, join the Network here: Sandoz Talentpool (novartis.com)
#Sandoz
Commitment to Diversity & Inclusion:
We...
...combines responsibilities in Medical Safety Operations (addressing pharmacovigilance (PV) needs) with broad Project Management activities.... ...internal key stakeholders/customers/partners through exhibiting Novartis values (inspired, curious, unbossed & self-aware) in Medical Safety...
Rs 6 - 8 lakhs p.a.
...firm in the Pharmaceutical & Life Sciences sector, trusted for its expertise and commitment. Specializing in Regulatory Affairs, Pharmacovigilance, and GxP Compliance, we offer tailored solutions through our unique Commit-Collaborate-Carry Model, aimed at enhancing patient...
Rs 8 - 9 lakhs p.a.
...Company Overview:
Pharmazone is a leading Consulting company specializing in Regulatory Affairs, Pharmacovigilance, and GxP Compliance solutions for global clients. With a strong legacy of trust, we strive to improve patients' lives through our unique Commit-Collaborate...
...on delivery
Resolution of escalations
Zero non-conformance on security or compliance requirements
3.
Team Management
Team attrition %, Employee satisfaction score, %technical trainings, %general trainings
Pharmacovigilance & Drug Safety(Pharma)
...Preferred: 01 year work experience in job areas such as: o Clinical trial coordinator at site
Clinical data management
Pharmacovigilance
Records management
Key Personal Attributes:
Highly personable nature that fosters teamwork
Excellent communication skills...
...publication in peer-reviewed journals on original research and review article.
Work in Clinical Trials, Regulatory Affairs, Pharmacovigilance etc.
Involves coordination with R&D, QA department, CROs for submission of dossiers for product registration.
Participates...
...and ensures timely close out w/ all proper documentation in Astellas systems.
Actively collect as well as guide PS to collect pharmacovigilance information such as adverse events (“AE”), special situations
KOL Relationship Management
Engage with potential...
...in the pharmaceutical industry.
Familiarity with digital health, competitive intelligence, disease understanding, statistics, pharmacovigilance, non-clinical and clinical pharmacology.
Knowledge of patient access, real-world evidence, and proficiency in written and...
...project.
• Support creation of post-marketing safety activities, such as PSMF, RMP and PBRER
• Support Qualified Person for Pharmacovigilance as required.
• Liaise with investigational site, reporter, and/or Sponsor as necessary regarding safety issues.
• Liaise with...
Remote job
...a bachelor’s degree in relevant subject with 12+ years of experience having 3+ years of practical experience in GLP/ GMP/ GCP/ pharmacovigilance areas.
~ Good to have experience as an ISO 9000 Lead Auditor or equivalent IT quality auditing experience.
~ Strong knowledge...
...and understanding of business management principles.
Knowledge of R&D value chain, digital health, competitive intelligence, pharmacovigilance, clinical pharmacology, market access, and real-world evidence generation preferred.
About the Department
The RA Labelling...
...ethnicities. We recognize this is our strength and celebrate it.
Key words: Aggregate Report Physician, MD, Medical Doctor, MBS, Pharmacovigilance, PV, GVP, Signal Management, Risk Management, Aggregate Report, PBRER, Clinical Research, CRO, Contract Research Organisation,...
...systematic errors, and potential lack of compliance or fraud across trials.
The Position: (Note: This is not a role within Pharmacovigilance)
The Key Responsibilities in this position will be to perform a Medical Review of all trial subjects of all assigned...