Average salary: Rs900,000 /yearly
More statsSearch Results: 5,036 vacancies
...development with a thorough understanding of data to be collected and in alignment with the... ...in assigned studies and provide clinical input into the development of new and updated... ...schedule for rapid data availability and review. Act as facilitator / problem solver between...
...Position: Clinical Data Manager
Requirement: Immediate Joiner
Location: Hyderabad
Experience: 3 to 10 Years
Key Roles & Responsibilities... ...and provide technical expertise.
Conduct performance reviews establish annual expectations for the team and provide coaching...
...About the role
Clinical Data Scientist
Location – Hyderabad/ Mumbai
About the Role:
Provide timely and professional ongoing management... ...the eCRF, CCG’s where needed, Data Handling plan (DHP) Data Review Plan (DRP) and performimg user acceptance testing (UAT) as...
Position : Clinical Data Analyst EPIC ClarityLocation : Pune/Hyderabad/GurgaonExperience : 3+Job Description :We are seeking a skilled and experienced Clinical Data Analyst to join our team and support our Epic Systems implementation. The ideal candidate will have a strong...
...Designation: Clinical Data Manager
Full Time Opportunity
Location: Full Time
Job Description:
- Tasks have been carried out independently and the status is communicated back to all relevant parties.
- Ensuring that the electronic data generated is transferred...
...Designation: Clinical Data Management
Full Time Opportunity
Location: Multiple
Job Description:
- Understand and follow study start... ...the Service Provider for the studies as assigned
- Prepare/review eCRFs, Edit checks, and Custom Functions requirement document...
...We are hiring for our MNC Client
Role : Data Analyst {Clinical Data Management}
Total Work Experience Range : 3 yrs- 5 yrs {Must have relevant... ...aspects that spanned :
1. eCRF design / UAT
2. Data review / query management
3. Edit check / SAS check specs...
...Job Tittle-Clinical Database Programmer Years of Experience- 4 to 10
Lead Clinical Database Programmer
Mumbai, Bangalore, Hyderabad
• A person should have 7 - 10 years of experience in Medidata RAVE Custom Function
Programming.
• Should have good knowledge...
...external guidelines, to compile and add electronic navigation to clinical and regulatory documents. Support the timely submission of documents... ...Project Management.
Skills:
Clinical Study Reports.
Data Analysis.
Documentation Management.
Lifesciences.
Operational...
...Lead and manage a multidisciplinary cross functional Clinical Trial Team (CTT) (medical writing, statistics, data management, monitoring partner, drug supply,... ...ensure smooth study set up and smooth study conduct, reviewing site performance, protocol deviations, ongoing risk...
Rs 7 - 9 lakhs p.a.
...Deliver timely consistent, accurate and reproducible coding of clinical trial data using industry standard
coding dictionaries (MedDRA,... ...requirements
defining coding elements, dictionary versions and review timelines.
• Complete and submit Medidata Project Registration...
...Process Associate - Content Review - Gujarati + English - HIG017172
Genpact (NYSE: G) is a global professional services and solutions... ...industry knowledge, digital operations services, and expertise in data, technology, and AI.
We are inviting applications for the role...
...Chartered Engineer - Construction Projects Review
FinacPlus provides Virtual Business and Professional Services to overseas clients and... ...required and must have the ability to summarize and present data efficiently.
LOCATION: Hyderabad
TIMINGS: 6:30pm to 3:3...
...Summary:
We are seeking a highly motivated and experienced Clinical Research Associate (CRA) with a minimum of 2-3 years of relevant... ...Perform routine monitoring visits to assess site performance, data integrity, and regulatory compliance. Ensure timely resolution of...
Summary
-Supports coordination, preparation and execution of clinical trial(s) and /or supporting activities within schedule, budget, quality /compliance and performance standards.
About the Role
Major accountabilities:
Contribute to one or more operational aspects...
...About the role
“150! Clinical scientific experts, globally, are part of Global Drug Development... ...) team, working to ensure clinical trial data and regulatory reports are of highest... ...ensuring high quality clinical trial data review/insights and analysis as directed by the Integrated...
...pharmacokinetics, pharmacodynamics, metabolism and clinical pharmacology in advancing the drug... ...at CRO which includes, contract review, assay development, validations in support... ...clinical trials ensuring accurate and timely data delivery.
• Support emerging new modalities...
...attacks, intrusions and unusual, unauthorized orillegal activity
# Performs moderately complex log reviews and forensic analysis toidentify unauthorized or unacceptable access to data or systems
# Conduct security assessments, risk analysis and root causeanalysis of security...
...Responsibilities
Support CRAs with the setup monitoring and closeout of clinical trials in accordance with Good Clinical Practice (GCP) ICH... ...in site qualification initiation and monitoring visits.
Review and track clinical trial documentation ensuring accuracy and completeness...
...creating an ambitious impact in an industry, then this role is for you!
Responsibilities
Strike appointments and meetings with Dental Clinic Owners and Hospital owners and renowned Doctors in the twin cities to introduce to them a new efficient way of procurement for their...
