Clinical Study Internships

1. Having an insight regarding the study materials shared and presenting the same to the concerned doctor 2. Completing the documents like Feasibility Questionnaire, Confidentiality Disclosure Agreement, Investigator Undertaking etc.. required for study Start-Up activity. 3.Collection of documents like calibration certificates, lab documents etc.. from the...

The Associate Director, Biostatistics and Statistical Programming is a key leader of the Flex Operations, Biostatistics and Statistical Programming Team, providing daily supervision of Biostatistics and Statistical Programming operations and personnel to ensure the achievement of departmental goals and levels. This role will plan, analyze, and summarize the...

**Job Title**:Clinical Data Associate**Job Location: Trivandrum, Kerala** **Job Overview**: The Clinical Data Associate assists the Clinical Data Manager with the process of cleaning and validating data in clinical trials in accordance with Clinipace SOPs, Good Clinical Practice, ICH Guidelines and sponsor requirements. **Job Duties and...

About Us:We are a global digital engineering and IT services company that specializes in modernizing technology infrastructure, adopting cloud and AI solutions, and accelerating innovation.Our team operates in over 50 locations across more than 25 countries, with delivery centers in Asia, Europe, and North America.Job Title: Clinical Research AssociateKey...

About the Clinical Trial Screening Interview Opportunity:We are seeking a skilled healthcare professional to collaborate with us as a freelance worker for conducting clinical trial screening interviews.The Role Requirements:Clinical trial screening interview collaboration on a freelance basisLocation: IndiaLanguages: Fluency in Kannada (India) is...

Sponsor-dedicated roles have become increasingly prominent in the industry.Working fully embedded within a pharmaceutical client, with the support of a global services provider right behind you, you'll be at the heart of their innovation. As a Senior Statistical Programmer you will be dedicated to one of our clients; a company that is driving the next...

As a Principal Statistical Programmer you will be a key member of the Development Operations, Statistical Programming Team. You will program routine and customized data displays, (including listings, tables, and graphics) in accordance with approved Statistical Analysis Plan and shell displays.  Additionally, you write CDISC compliant SDTM specifications...

Key Clinical Document Specialist RoleWe are seeking a highly skilled professional to develop high-quality clinical trial documents and translate complex scientific data into clear, regulatory compliant documents that support drug development and approval processes.Main Responsibilities:Develop key clinical trial documents, including protocols, Investigator's...

As a seasoned Lead Biostatistics Professional, you will spearhead the development and implementation of cutting-edge statistical strategies for clinical trials. This role involves contributing to the planning, execution, and interpretation of advanced statistical analyses, ensuring high-quality deliverables that meet regulatory and scientific standards.Key...

MUST HAVE: SAS Certification / Internship AND Education: BTech, MTech, MCA, or MSc AND Office-Based in Trivandrum ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of...