Key Responsibilities: Educational Qualification: Experience: 7-10 Years Behavioural Skills: Technical/functional Skills: • Ability to comprehend scientific information• Good understanding of clinical research.• Knowledge of working on MS word, PPT etc.• Attend training on environment, health, and safety (EHS) measures imparted company ...
Clinical Research Jobs Latest Articles
Study Personnel
CRI1Key Responsibilities Educational Qualification Technical/Functional Skills Experience Behavioral Skills Apply: https://www.linkedin.com/jobs/view/4088729224/?alternateChannel=search&refId=DsRKOj%2BhXpB%2Bhsbst2bWyA%3D%3D&trackingId=CAbkqHntIYrBtthutY%2F0zA%3D%3D
Clinical Data Specialist
CRI1Summary Of Responsibilities Qualifications (Minimum Required) Experience (Minimum Required) Physical Demands/Work Environment Apply: https://www.linkedin.com/jobs/view/4119723214/?alternateChannel=search&refId=DsRKOj%2BhXpB%2Bhsbst2bWyA%3D%3D&trackingId=QqQTXqkkZKzrQpwMqUtyHQ%3D%3D
Senior Analyst – Clinical Development
CRI1Key responsibilities Skills & Activities Education & Experience Apply: https://www.linkedin.com/jobs/view/4116759344/?alternateChannel=search&refId=DsRKOj%2BhXpB%2Bhsbst2bWyA%3D%3D&trackingId=exJj%2Bniy7knTa0dDlXCHAA%3D%3D
Associate Data Manager – Clinical Data Sciences
CRI1Participate in CDS activities including data review and query management, assist with quality database design including documentation, testing, validation, and implementation of clinical data collection tools, CRF and non-CRF, using an electronic data capture (EDC) system and/or other data collection ...
Data Manager, Clinical Data Sciences
CRI1Job Summary: As part of the Clinical Data Sciences (CDS), an integral delivery unit within the Global Biometrics and Data Management (GBDM) organization, the Data Manager is responsible for timely and high quality data review and query management of clinical ...
Clinical Trial Assistant
CRI1JOB DETAILS• Assist Project Manager with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.• Assist the PM in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the ...
Clinical Trial Manager ((Cardiovascular, Renal & Metabolic Disease (CVRM))
CRI1Responsibilities The Clinical Trial Manager position performs project lead role for multiservice global clinical trials. The position interacts with sponsors and manages the timeline and project deliverables. This role coordinates for all services contracted for the study. CTMs are also ...
Clinical Trial Supply Manager
CRI1About The Role HSEMajor accountabilities: Minimum Requirements Work Experience: Skills Languages Apply: https://www.linkedin.com/jobs/view/4119574243/?alternateChannel=search&refId=%2BXMfsvwpSd58zdPYo%2Bup%2Fg%3D%3D&trackingId=KGBl3yXvu4BS6l19ySFCZA%3D%3D
Clinical Research Associate
CRI1Job Responsibilities Job Requirements Apply: https://www.linkedin.com/jobs/view/4087969059/?alternateChannel=search&refId=%2BXMfsvwpSd58zdPYo%2Bup%2Fg%3D%3D&trackingId=rppFJzQ0NO87Slq0VKd8KA%3D%3D
Clinical Research Associate
CRI1Responsibilities Clinical Research Associate Job Description Additional Responsibilities May Include Qualifications Apply: https://www.linkedin.com/jobs/view/4090930955/?alternateChannel=search&refId=%2BXMfsvwpSd58zdPYo%2Bup%2Fg%3D%3D&trackingId=3ZqkzFNUzktP3%2BX0t%2BpLbQ%3D%3D
Clinical Trial Manager II
CRI1Location: India-Asia Pacific – IND-Home-Based, India Job responsibilities• Responsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance and data integrity. • Oversees site interactions post activation through site closeout. This may include ...
Sr Clinical Coder
CRI1Job responsibilities • Lead experience in multicenter large clinical trials.• Involvement in protocol and DB build process.• Proven record of Lead experience in multicenter large studies.• Experience in liaison with sponsor counter parts on Coding convention, Specification, and coding decision process.• ...
Clinical Trial Manager
CRI1Role Summary Responsible for study oversight and delivery management (time, budget, quality) at country level from start-up to closure. Key Responsibilities Additional responsibilities: Degree/Certification/Licensure: Experience – Responsibility and minimum number of years Competencies – knowledge, skills, abilities, other Software that ...
Assoc, QA – Batch Release
CRI11 To review executed Batch Manufacturing Records and Batch Packing Records.2 To ensure that every batch record is reviewed for its accuracy, completeness, and compliance with the established specifications to determine its disposition for release or reject.3 To review all ...