Hbr Layout Bengaluru Karnataka Clinical research associate Jobs – 73 Open Jobs Today

Clinical Data Associate II
Precision for Medicine —Bengaluru, Karnataka
- Online application
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
Biostatistics - Associate Statistician
YOUV Research —Bengaluru, Karnataka
- Bachelor's degree
Associate Regulatory Specialist
Novo Nordisk —Bengaluru, Karnataka
- Doctoral degree
- English
- Master's degree
6h
Pharmacovigilance Services Analyst
Accenture —Bengaluru, Karnataka
- Full-time
- Master's degree
- Bachelor's degree
- Data entry
7d
Associate Director, Clinical Program Management
Takeda Pharmaceutical —Bengaluru, Karnataka
- Full-time
- English
- Bachelor's degree
- Travel
Clinical Data Svs Sr Analyst
Accenture —Bengaluru, Karnataka
- Full-time
- Master's degree
- Bachelor's degree
- Communication skills
Quality Assurance Associate
Accenture —Bengaluru, Karnataka
- Full-time
- English
- Master's degree
- Bachelor's degree
Mgr, Centralized Monitoring
IQVIA —Bengaluru, Karnataka
- Full-time
- English
- Bachelor's degree
- Training & development
1d
Ai Associate
MS CLINICAL —Bengaluru, Karnataka
- Research
- Java
- Databases
13d
CRAII
Emmes Group —Bengaluru, Karnataka
- Full-time
- Remote
- Microsoft Office
- Bachelor's degree
- Organizational skills
Clinical Data Svs Associate Manager
Accenture —Bengaluru, Karnataka
- Full-time
- Project management
- Bachelor's degree
- Cleaning
2d
Associate Medical Safety director
IQVIA —Bengaluru, Karnataka
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Medical Science Liasion
Novartis —Bengaluru, Karnataka
- Full-time
- Medicine
- Doctoral degree
- English
10h
Sr Mgr Biostatistics
Teva Pharmaceuticals —Bengaluru, Karnataka
- Doctoral degree
- Master's degree
- Communication skills
- Health insurance
8d
Associate IT Operations Administrator
Emmes Group —Bengaluru, Karnataka
- Full-time
- Microsoft Outlook
- Computer Science
- Software troubleshooting
1d
Data Entry Associate I
Labcorp —Bengaluru, Karnataka
- Full-time
- Master's degree
- Bachelor's degree
- Data entry
4h
Research Associate (Contract) Outbound Calling
m360 Research —Bengaluru, Karnataka
- English
- Project management
- Organizational skills
Quick apply
6d
Business Analyst
Eurofins GSC IT DC —Bengaluru, Karnataka
- Full-time
- B.Sc
- Laboratory experience
- English
Quick apply
13d
Senior Medical Writer
Navitas Life Sciences —Bengaluru, Karnataka
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Medicine
Associate
EVERSANA —Bengaluru, Karnataka
- Full-time
- Microsoft Powerpoint
- Master's degree
- Databases
Quick apply

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Clinical Data Associate II

Precision for Medicine -
Bengaluru, Karnataka

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Job details

Qualifications

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Microsoft Outlook
Clinical research
SAP
English
Microsoft Office
Bachelor's degree
Data entry
Communication skills

Full job description

Position Summary:

The Clinical Data Associate II provides data management support and assistance in all aspects of the clinical trial data management process from study start up to post database lock for assigned projects under direct supervision. Standard Operating Procedures / Work Instructions (SOPs/WIs); regulatory directives; study specific plans and guidelines will be followed. This position may perform database development and testing, as well as additional data management activities.

Essential functions of the job include but are not limited to:

Support the Lead DM as a back-up and/or team member, ensuring continuity, responsiveness, and that tasks are performed in a timely manner
May perform data entry for paper-CRF studies, as needed
May perform quality control of data entry
May develop CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholders
May assist in building clinical databases
Conduct database build UAT and maintain quality controlled database build documentation
Assist in specifying requirements for all edit check types e.g. electronic, manual data review, edit checks, etc.
Responsible for creating, revising, appropriate versioning and maintaining data management documentation.
Train clinical research personnel on the study specific CRF, EDC, and other project related items as needed
Review and query clinical trial data according to the Data Management Plan
Assist in line listing data review based on the guidance provided by the sponsor and/or Lead DM
Run patient and study level status and metric reporting
Perform medical coding of medical terms relative to each other in order to ensure medical logic and consistency
Assist with coordinating SAE/AE reconciliation
Assist with liaising with third-party vendors such as external data and EDC vendors in a project-manager capacity in support of timelines and data-related deliverables
May assist with SAS programming and quality control of SAS programs used in the Data Management department
May assist in identifying and troubleshooting operational problems, issues, obstacles, and barriers for studies based on metrics data, audit reports, and input from project team members and other stakeholders
May assist in reviewing and providing feedback on protocols, Statistical Analysis Plans (SAP) and Clinical Study Reports (CSRs), if required by the project
May assist in participating in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to data management and database management activities
Communicate with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issues
May present software demonstrations/trainings, department/company training sessions, present at project meetings
May require some travel
Perform other duties as assigned

Qualifications:

Minimum Required:

Bachelors and/or a combination of related experience

Other Required:

2 to 4 years' experience
Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook
Able to handle a variety of clinical research tasks
Excellent organizational and communication skills
Professional use of the English language; both written and oral

Preferred:

Experience in a clinical, scientific or healthcare discipline

Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected].

It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.

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Refine Your Search

clinical research associate jobs in hbr layout bengaluru karnataka

Clinical Data Associate II

Biostatistics - Associate Statistician

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CRAII

Clinical Data Svs Associate Manager

Associate Medical Safety director

Medical Science Liasion

Sr Mgr Biostatistics

Associate IT Operations Administrator

Data Entry Associate I

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Business Analyst

Senior Medical Writer

Associate

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