Search Results: 3,032 vacancies
...with the setup monitoring and closeout of clinical trials in accordance with Good Clinical... ...GCP) ICH guidelines and company SOPs.
Assist in site qualification initiation and monitoring... ...Health
Strong interest in clinical research and drug development.
Excellent...
...Summary:
We are seeking a highly motivated and experienced Clinical Research Associate (CRA) with a minimum of 2-3 years of relevant experience... ...protocol-related queries.
Regulatory Compliance:
Assist in the preparation and submission of regulatory documents to ethics...
...Overview
Ondezx is a globally trusted organization providing PhD assistance to thousands of scholars all around the world who are in need... ...We are seeking a highly motivated and detail-oriented Research Assistant to join our team in Hyderabad, Telangana, India. As a...
...Business Development
Strategy & Services
Client Handling
New Client Acquisition
Regulatory Affairs
business development,strategic business,clinical research,projects,communication skills,new client acquisitions,global business strategy,regulatory affairs...
About the Role
Clinical Project Manager
Location – Hyderabad #LI Hybrid
About the Role:
This role is responsible to Lead and... ...evaluation and implementation of assigned clinical studies and/or MAP//Research Collaborations/IIT/Digital Solutions programs according to...
...JOb Role: Clinical Manager
Location: Pune/Hyd/Bangalore
JOB DESCRIPTION :
• Should be trained on SCM (Sunrise Clinical Manager) & Pharmacy Module (SMM)
• Should well versed with SCM Configuration Tools
• Should have build experience/expertise in Pharmacy (Generic...
Summary
Responsible to execute clinical services and meet planned deliverables in line with defined roles and responsibilities agreed... ...clinical study execution in a pharmaceutical company or contract research organization.
Experience in finance: forecast, actuals, cost...
...collected and in alignment with the protocol.
Support the assessment of new data collection requirements in assigned studies and provide clinical input into the development of new and updated clinical Data Standards (for CRFs as well as 3rd party data collection methodologies)...
...of appropriate oversight and tracking of TMF QC activities.
• Execute trial TMF QC activities in accordance with TCO portfolio and Clinical Operations Transition Decision Point (TDP) and Clinical Study Report (CSR) dates. Support CTTs with audit/inspection prep activities....
...people support 245+ active projects and clinical trials across 50+ countries, with 400+ more... ...clinical, population and health systems research.
Our experts are among the most cited... ...Research Associate would be expected to :
- Assist in the development of trial related...
Rs 7 - 9 lakhs p.a.
...Deliver timely consistent, accurate and reproducible coding of clinical trial data using industry standard
coding dictionaries (MedDRA... ...3 years’ Clinical Data Coding experience in support of clinical research.
• Indepth knowledge of industry standard coding thesauri (MedDRA...
...TM), in Novartis Institutes of Biomedical Research (NIBR). It is an enterprise organization,... ..., pharmacodynamics, metabolism and clinical pharmacology in advancing the drug candidates... ...assay development and qualification, used to assisting with LBA method troubleshooting across a...
Role: Senior Clinical SAS Programmer
Work Location: Hyderabad/Bangalore/Mumbai/Pune/Delhi/Kolkata
Experience Range: 5 to 12 years in ADaM, TLF
Job Description:
• Thorough understanding of ADAM concepts and challenges. Good hold on the TAUG’s and related guidelines...
Responsibilities
● Serve as teaching & Research Associate for multiple courses as part of the PGDM curriculum
● Assist the Program Office in research & teaching-related activities, including literature reviews, data collection, data analysis, managing research databases, and...
...Associate Clinical Data Manager
SDC is a team of diversified professionals who deliver... ...support of clinical and/or non-clinical research studies for study initiation, setup, maintenance... ...data management on multiple studies
• Assist Clinical Data Managers or Project...
...of the LCTL/CTL, as assigned. Support the clinical protocol development process in... ...operational procedures: attend CTT meetings, assist in report study progress and issues.
support... ...Department as well as with the Assay Research Lab. This also includes the set-up, logistics...
...talented people in the industry.
Senior Clinical Data Associate
Job Summary:... ...management activities in support of clinical a research studies as a senior member of Data Review... ...resolution on multiple studies as
needed to assist lead Clinical Data Managers
• Performs...
...About the role
“150! Clinical scientific experts, globally, are part of Global Drug Development (GDD) team, working to ensure clinical... ...).
•
1 year experience in pharmaceutical industry/ clinical research organization - Basic knowledge in planning, executing, reporting...
...Position: Clinical Data Manager
Requirement: Immediate Joiner
Location: Hyderabad
Experience: 3 to 10 Years
Key Roles & Responsibilities... ...SMEs and universities to establish a global forum for clinical research technologies.
Qualifications:
Bachelor s or Master s...
...Applications are invited for the post of Assistant Professor, School of Sciences, Woxsen University... ...Hyderabad. This role involves teaching, research and administrative work.
Job Details:... ...PhD degree in Biotechnology, clinical microbiology, and clinical biochemistry....
