Doha, Al Wakrah, Qatar
$10/hr · Starting at $25
Considerable drug safety knowledge and experience in pharmacovigilance/drug safety profile. More than 9 years of experience in Pharmacovigilance (PV) with expertise in management of Individual Case Sa…
Greater Noida, Uttar Pradesh, India
$10/hr · Starting at $100
Ensuring Individual Case Safety Report (ICSR) case processing and related activities are carried out to enable compliance with applicable regulatory requirements, company procedures, at a local/region…
New Delhi, Delhi, India
$12/hr · Starting at $60
B.Pharma and MBA worked with 3 multinational firms.Can do End to end PV including data entry in ARgus Arisg , narrative writing, literature article ICSRs litigation End to end processing of literatur…
Mysuru, Karnataka, India
$8/hr · Starting at $25
Authoring and reviewing of PBRER, PSUR and PADERs. Also expert in performing end to end activities of ICSRs
Chandigarh, Chandigarh, India
$25/hr · Starting at $25
Five years of experience of ICSR review as per Client specific DEG and ICH guidelines. MeDRA coding and Expectedness.
Pune, Maharashtra, India
$7/hr · Starting at $70
We are the best service provider in Pharmacovigialnce ICSR case processing. I'm a pharmacovigilance professional and having a more than 10 years of experience in ICSR case processing, quality review a…
Dehradun, Uttarakhand, India
$5/hr · Starting at $25
I have about 3 years of experience in Pharmacovigilance case processing, coding with Meddra, WHO DD. Worked with Pharma Giant. Well versed with the Argus database. End to end processing of ICSR. Causa…
Dakor, Gujarat, India
$50/hr · Starting at $30
Associate Manager Handling all the lead activities for the assigned project Responsible for prioritization of cases, ensure daily reconciliation activities and daily work flow management. Prioritizat…
Hyderabad, Telangana, India
$50/hr · Starting at $50
Physician with 2+ years of experience. Looking for Freelance Medical reviewer role. Expertise on Case processing and ICSR handling.
Mumbai, Maharashtra, India
I have more than 3 years of experience in Pharmacovigilance case processing, coding with meddra, WHO DD. Well versed with the Argus database. End to end processing of ICSR. Including the finalizations…
Ghaziabad, Uttar Pradesh, India
$11/hr · Starting at $25
hello, I have 2 years expereince in pharmacovigilance that is in case processing, case triaging, narrative writing, case processing from ICSR, spontaneous,FDA reporting.
wixom, Michigan, United States
ID Verified
My team offers a full range of pharmacovigilance consulting from small scale to large scale operations. We assist in creation, review, and finalization of documents (Aggregate Reports, contracts, SOP…
$10/hr · Starting at $30
Medical assessment of the case for seriousness, listedness/labeling, causality, adverse event MedDRA coding and narrative review. Highly efficient in working as per regulatory requirements. Review of
$15/hr · Starting at $100
I have more than 7.5 years of experience in clinical research industry. My experience includes, but not limited to, preparation of regulatory documents including PBRERs/PSURs, Addendum to PBRER/PSUR;
T'bilisi, T'bilisi, Georgia
$5/hr · Starting at $30
I had a very god experience in PV end to end processing. Expert in Argus safety database. Started my career in Accenture India operations. And i moved to Georgia, Worked as a freelancer for a while. I…
I have 6 years of experience in data entry of various types of cases including literature, non-literature and other types as well. I also have experience in triage of literature articles for ICSR, PSU…
Bengaluru, Karnataka, India
$55/hr · Starting at $45
I am a medical professional with 8plus years of experience in pharmacovigilance in the fields of ICSR processing, medical review, aggregate report writing, signal detection, RMP and pharmacovigilance
Gurgaon, Haryana, India
$15/hr · Starting at $50
I have over 5 years of experience in field of Pharmacovigilance Management with an immense knowledge of narrative writing for Clinical Study Report (CSR). I have lead and managed approximately 5-6 stu…
Lisboa, Lisboa, Portugal
Liason with quality team, production team, clinical team (~20 people) - Lifecycle management of Medicinal Products for Human use, Skills on Regulatory affairs (EudraLex Vol.2), Market access, Pharmaco…
$30/hr · Starting at $1,000
Processing and management of ICSRs including Case intake, Case entry, MedDRA and WHO-DD coding, Triaging, Quality Control, Medical review etc) Generation of Regulatory reports including Expedited, PSU…