India – Mumbai JOB RESPONSIBILITIES · Participate 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 ...
Clinical Research Jobs Latest Articles
Clinical Statistician
Clinicalresearchinfo
India – Chennai ROLE SUMMARY BASIC QUALIFICATIONS PREFERRED QUALIFICATIONS Apply here: https://pfizer.wd1.myworkdayjobs.com/en-US/PfizerCareers/job/India—Chennai/Clinical-Statistician_4913183?q=clinical&source=linkedin&locations=e2d3979e3af101936db42457076cbe8e&locations=e2d3979e3af1014c8c757857076c0e8f
Study Coordinator
Clinicalresearchinfo
Bangalore, India 1. Data Analysis and Reporting: Performs initial review of bioanalytical data and originates noncompartmental analysis (NCA) in support of pharmacokinetic and toxicokinetic studies. Aids in report preparation, including tables and figures. 2. Study Conduct: Serves as the primary contact ...
Associate Study Coordinator
Clinicalresearchinfo
Bangalore, India 1. Protocol Familiarization: Learn to read and comprehend study protocols, sample analysis outlines, amendments, and study schedules, ensuring understanding of regulatory requirements. 2. Data Analysis and Reporting: Performs initial review of bioanalytical data and originates noncompartmental analysis (NCA) ...
In-House CRA
Clinicalresearchinfo
(Senior) Clinical Trial Assistant Location: Office-based/ Hybrid, Sydney (Australia) What you will be doing: You are: Apply here: https://careers.iconplc.com/job/in-house-cra-in-sydney-jid-35246
(Senior) Clinical Trial Assistant
Clinicalresearchinfo
Location: Home-based, Queensland (Australia) What you will be doing: You are: Detail-orientated, passionate and reliable. Apply here: https://careers.iconplc.com/job/senior-clinical-trial-assistant-in-australia-jid-35637
Senior Medical Writer
Clinicalresearchinfo
Australia The role:• Responsible for writing and reviewing study documents such as Protocol, Synopsis, Informed Consent, Data Collection Documents and Study Report, etc.• Responsible for developing scientific communication such as abstract, poster, manuscript, etc.• Responsible for performing quality control for ...
Study Start Up Associate II
Clinicalresearchinfo
Country: Australia or New Zealand Working schedule: Permanent headcount, office based (Australia), remote based (New Zealand) The Role: Collect, prepare, review, approve, process and track regulatory and site level critical documents required for study site activation in accordance with SOPs/WPs, ...
Site Management Administrator
Clinicalresearchinfo
Country: Australia (Office based; Sydney and Melbourne locations) The Role: • Assists in identifying study sites by performing site feasibility and recruitment tasks, e.g., completing, disseminating and reviewing responses to site recruitment questionnaires. • Completes essential document collection and review ...
Senior Clinical Research Associate
Clinicalresearchinfo
Location: Home-based in Melbourne (preferred) or Sydney What you will be doing: You are: Apply here: https://careers.iconplc.com/job/senior-clinical-research-associate-in-melbourne-sydney-jid-36022
Clinical Research Associate
Clinicalresearchinfo
About the role Clinical Research Associate Location: Home-based in Sydney or Melbourne What you will be doing: You are: Apply Here: https://careers.iconplc.com/job/clinical-research-associate-in-melbourne-sydney-jid-35782
CRA II
Clinicalresearchinfo
Location: ICON, Australia The role:• Independent, proactive work to set up and monitor studies, complete reports and maintain documentation• Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions• Balancing sponsor generated queries• Taking responsibility for study ...
Senior CRA
Clinicalresearchinfo
About the role Senior Clinical Research Associate Location: Australia, Home-based As a Senior Clinical Research Associate you will play a key role in improving the lives of patients by accelerating the development of our customers’ drugs and devices through innovative ...
Associate Study Coordinator
Clinicalresearchinfo
1. Protocol Familiarization: Learn to read and comprehend study protocols, sample analysis outlines, amendments, and study schedules, ensuring understanding of regulatory requirements and Labcorp SOPs/P&Ps relevant to client deliverables. 2. Data Analysis and Reporting: Performs initial review of bioanalytical data ...
Management Trainee – Early Talent Program
Clinicalresearchinfo
These responsibilities include some of the following: · Implement projects while meeting the scope, schedule and costs · Ensure compliance with GSK procedures, policies, and standards are met · Submission of projects, preparation of documents necessary for the implementation of the investment and ...