Fresher Hiring in Pharmacovigilance, Clinical Trial Coordinator, CDM, Records Management | Research Analyst

Fresher Hiring in Pharmacovigilance, Clinical Trial Coordinator, CDM, Records Management | Research Analyst
  • Freshers
  • Full Time
  • Bengaluru

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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Perks 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

  • Extract and interpret key information from clinical trial study documents.
  • Utilize Advarra’s Clinical Trial Management Software (CTMS) for project development and support.
  • Collaborate with cross-functional teams to ensure projects meet pre-determined quality standards.
  • Review existing processes and optimize performance for research efficiency.
  • Actively contribute to team meetings and discussions to advance project goals.

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
Fresher Hiring in Pharmacovigilance, Clinical Trial Coordinator, CDM, Records Management | Research Analyst
Fresher Hiring in Pharmacovigilance, Clinical Trial Coordinator, CDM, Records Management | Research Analyst

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.

Apply Now at Advarra Careers

Tagged as: Global Pharma Jobs, Good Clinical Practice (GCP), Pharmaceutical Careers, Pharmaceutical Jobs

To apply for this job please visit recruiting.ultipro.com.


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