Fresher Hiring in Pharmacovigilance, Clinical Trial Coordinator, CDM, Records Management | Research Analyst
- About the Role
- Why Join Advarra?
- Key Responsibilities
- Qualifications
- Preferred Skills
- Physical Requirements
- Location
- How to Apply
Join Advarra as a Research Analyst in Bengaluru. Freshers with 0–2 years’ experience in Pharmacovigilance, Clinical Data Management, Records Management, or Clinical Trial Coordination are welcome to apply. Discover an inclusive workplace and build your future in clinical research.
About the Role
Advarra is seeking fresh graduates to join our team as Research Analysts at our Bengaluru office. Become part of an organization that is at the forefront of revolutionizing clinical research and human health.
Why Join Advarra?
At Advarra, we lead with purpose, breaking silos to unify patients, sites, sponsors, and CROs within a connected global ecosystem. Our inclusive work environment values diversity, encourages collaboration, and fosters growth.
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📱 Join Click HerePerks of Joining Advarra:
- Work with market leaders in the clinical research field.
- Participate in initiatives that advance human health and clinical trials.
- Enjoy an inclusive culture with professional growth opportunities.
Key Responsibilities
- Understand and interpret clinical trial study documents to extract the required information for various tasks.
- Develop a familiarity with Advarra’s Clinical Trial Management Software (CTMS) to utilize related functionalities in the design, development, and support of various services.
- Ensure that projects are completed in accordance with agreed-upon requirements by working with the project managers and the internal team.
- Ability to review and repurpose existing content to optimize effectiveness and productivity.
- Ability to work within cross-functional teams and verbally communicate ideas and information.
- Problem-solving and resolution of issues/bugs, quality, and detail oriented.
- Work closely with the reporting manager to complete daily/ weekly tasks to meet pre-determined quality criteria.
- Actively participate in team meetings and contribute meaningfully to discussions related to specific customer cases and/or protocols.
Qualifications
We’re looking for candidates who meet the following criteria:
Education & Experience
- Bachelor’s degree in Life Sciences, Pharmacy, or a related field.
- Freshers or candidates with up to 2 years of experience in the following areas are encouraged to apply:
- Clinical data management (CDM)
- Pharmacovigilance
- Records management
- Clinical trial coordination
Additional Requirements
- Knowledge of clinical research methodologies and ICH GCP guidelines.
- Familiarity with MS Office tools and business software.
- Strong organizational and administrative abilities.
- Excellent communication skills (oral and written).
Preferred Skills
- Collaborative mindset to work within diverse teams.
- Detail-oriented approach to quality and problem-solving.
- A proactive attitude and willingness to take ownership of projects.
Physical Requirements
- Ability to work in a hybrid model at our Bengaluru office.
- Ability to sit or stand for extended hours and handle objects up to 10 lbs.
Location
Bengaluru, India — This position supports a hybrid working environment with flexibility.
How to Apply
Are you looking to start your clinical research career with a global leader? Join Advarra today. Apply now to take the next step in your professional development in an empowering and inclusive workplace.
To apply for this job please visit recruiting.ultipro.com.