Clinical Data Management & Analytics Jobs
This job information is taken from a company career websites. Since these jobs are Private company jobs, every day the jobs/vacancies may be filled by internal reference also. so, don’t be depressed and keep trying.Apply for Clinical Data Management Jobs by clicking the website link.
| Organisation | Job Title | Work profile | Qualificaltion | Experience | Link |
|---|---|---|---|---|---|
| Labcorp | Clinical Data Analyst | data management tasks, Assist with review clinical trial data in accordance with Data Management Plans | Relevant – Bachelors | – | Apply |
| Labcorp | Statistical Programmer II (Medical Devices) | Develop, maintain, and validate SAS programs under the direction of senior programming or biostatistics staff With support from senior programming staff, develop specifications for datasets or TLFs as needed | Relevant – Bachelors | 1-2 years of SAS® programming experience in the CRO | Apply |
| Labcorp | Nonclinical Data Associate I | Dataset Preparation, Drafting and finalizing nonclinical datasets with supervision | Relevant – Bachelors | (entry level position) | Apply |
| Labcorp | Validation Reviewer I | Create and Execute validation test scripts, Assist in creation of error tracking logs. etc | Relevant – Bachelors | – | Click here |
| Labcorp | Validation Analyst | Create and Execute validation test scripts and document the test results. etc | Relevant – Bachelors | – | Click here |
| Labcorp | Medical Writing Publisher – I | Related Work | Bachelor of Science/Arts (BS/BA) degree. | 0 to 2 + years | Click here |
| Labcorp | Data Information Services Associate I (Preferred Toxicology experience/Spot fire/ Pre clinical) | learning the tasks required of populating and querying databases with supervision. | Relevant | Entry level with Preferred Toxicology experience/Spot fire/ Preclinical) | Apply |
Pre-Clinical & Clinical Research Jobs
| Organisation | Job Title | Work profile | Qualificaltion | Experience | Website Link |
|---|---|---|---|---|---|
| Syngene | Clinical Trial Assistant / Project Associate | Assist Clinical Project Manager (CPM) and Clinical Research Associates (all levels) by accurately updating and maintaining clinical systems that track site compliance and performance | Bachelor’s/Master’s Degree in Life Science /B Pharmacy | 0 – 3 years in Clinical Research | Click |
Production, QA, QC Jobs
| Organisation | Job Title | Work profile | Qualificaltion | Experience | Website Link |
|---|---|---|---|---|---|