Advarra Hiring for Research Associate II for clinical research professionals in Bengaluru with hybrid work options and strong growth opportunities.
Advarra, a global leader in clinical research support services, has announced openings for the position of Research Associate II. This role is designed for candidates who possess knowledge of clinical research operations, Good Clinical Practice (GCP) guidelines, and the ability to work with clinical trial documents, budgets, and electronic data systems. With a hybrid work model in Bengaluru, India, this position provides an excellent opportunity for those looking to build a meaningful and long-term career in the clinical research industry. Advarra Hiring for Research Associate II
In this detailed post, you will find the complete job description, company background, roles and responsibilities, qualifications, required skills, workplace culture, and step-by-step instructions on how to apply. Advarra Hiring for Research Associate II
About Advarra
Advarra is recognized across the global clinical research community for its commitment to elevating research quality and efficiency. With a strong foundation in ethical review services and advanced technology solutions, Advarra plays a significant role in enhancing clinical trial operations. The organization aims to create an integrated ecosystem connecting key stakeholders such as patients, research sites, sponsors, and CROs in order to streamline and accelerate clinical trials. Advarra Hiring for Research Associate II
The company’s mission revolves around advancing human health by supporting safe, efficient, and ethically-sound clinical research processes. With decades of industry expertise and a growing global presence, Advarra continues to build innovative tools and frameworks that simplify clinical operations for research institutions and life sciences companies. Advarra Hiring for Research Associate II
Company Culture
At Advarra, employees form the core of the organization. The company prioritizes the well-being, development, and empowerment of its workforce. The workplace culture is shaped around core values such as: Advarra Hiring for Research Associate II
Patient-Centric Approach
Every action is guided by the goal of ensuring safety and well-being of clinical trial participants. Employees work with dedication, knowing their contributions directly impact human health outcomes. Advarra Hiring for Research Associate II
Ethical Conduct
Ethics form the foundation of all operations. The company maintains strict compliance with industry regulations, ethical review standards, and global guidelines.
Quality Focus
Advarra emphasizes accuracy and excellence in every project. The team consistently aims to meet and exceed high-quality benchmarks.
Collaborative Working Style
Cross-functional teamwork, open communication, and mutual respect define the collaborative spirit at Advarra. Employees are encouraged to share ideas, support each other, and contribute to innovative solutions.
The organization also promotes diversity, equity, and inclusion. Advarra is committed to building an environment where differences are valued, employees feel respected, and everyone has an equal opportunity to grow. Advarra Hiring for Research Associate II
Job Title
Research Associate II
Job Location
Bengaluru, India
(Available in hybrid or fully remote model for eligible candidates)
Job Type
Full-Time
Posting Date
November 18, 2025
Job Responsibilities
The Research Associate II role is a key operational position focused on designing, interpreting, and developing essential clinical trial documentation. The responsibilities include: Advarra Hiring for Research Associate II
1. Understanding Clinical Trial Protocols
The associate must interpret detailed clinical trial study protocols to create accurate calendars used for study planning, tracking, and scheduling.
2. Budget Development
Candidates need to interpret clinical trial agreements and sponsor budgets to develop site budgets for each assigned study protocol. This requires strong analytical skills and attention to detail.
3. Case Report Form (CRF) Design
The role includes designing and developing Case Report Forms (CRFs), which are crucial tools used for capturing clinical trial data consistently and accurately.
4. Working with Advarra’s CTMS and EDC
The associate will be trained to use Advarra’s proprietary Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) system. These tools are essential for building calendars, budgets, financial documents, and CRFs.
5. Daily and Weekly Task Completion
The candidate is expected to coordinate closely with the reporting manager to ensure timely completion of deliverables such as calendars, budgets, and CRFs while meeting predefined quality standards.
6. Using Case Management and Reporting Software
Tracking daily and weekly tasks in internal case management systems is essential. This ensures proper documentation, transparency, and workflow optimization.
7. Participation in Team Meetings
Active involvement in team discussions, presenting insights, addressing protocol-specific queries, and contributing to problem-solving is part of the everyday role.
Eligibility Criteria
Basic Qualifications
- Minimum 1 year of relevant experience in clinical research or associated fields
- Understanding of clinical research methodology, trial operations, and Good Clinical Practice (GCP) guidelines
- Ability to work both independently and within a team environment
- Strong organizational and administrative skills
- Familiarity with MS Office applications and standard business software tools
Preferred Qualifications
Candidates with experience in any of the following areas will be preferred: Advarra Hiring for Research Associate II
Clinical Trial Coordinator (Site-Level Experience)
Understanding of site operations, patient visits, and site budgets is valuable.
Clinical Data Management
Experience with CRF design, data entry, query management, or EDC systems will be an advantage.
Pharmacovigilance (Drug Safety)
Knowledge of case safety reports and medical data review can strengthen the application.
Records Management
Experience in handling trial documents, regulatory files, or clinical archives is an added bonus.
Physical and Mental Requirements
- Ability to sit or stand at a workstation for long periods
- Capability to carry, lift, or move objects up to 10 lbs
- Strong focus and ability to comprehend instructions
- Effective verbal communication skills
- Ability to manage tasks with attention to detail
Equal Opportunity Commitment
Advarra is an equal opportunity employer that follows strict nondiscrimination policies. The company ensures a fair workplace free from harassment or bias. Hiring decisions are made without consideration of race, color, religion, gender identity, sexual orientation, national origin, age, disability, genetic information, or any other legally protected characteristic. Advarra Hiring for Research Associate II
Advarra also takes active steps to ensure equal treatment of all employees in areas such as hiring, promotion, compensation, training, and professional development. Advarra Hiring for Research Associate II
How to Apply
Candidates who meet the eligibility criteria and wish to apply for the Research Associate II position at Advarra can follow the steps below: Advarra Hiring for Research Associate II
- Visit the official Advarra careers page.
- Search for the job title “Research Associate II – Requisition Number RESEA003883”.
- Review the job details and ensure that your qualifications match the requirements.
- Click on Apply Now to begin the application process.
- Create an account or sign in if you already have one.
- Upload your updated resume and fill in the required information.
- Submit the application and note any confirmation details for future reference.
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