eAspire Hiring For Clinical Data Management , Medical Writer, Pharmacovigilance , and R&D | Freshers Only

eAspire Technolabs Inc. is hiring for four positions in the pharmaceutical, biotechnology, and clinical research domains in Ahmedabad. The openings include Clinical Data Management Associate, Medical Writer, Pharmacovigilance Associate, and Research Associate.

Candidates with qualifications in Pharmacy, Pharm.D, Life Sciences, Biotechnology, Microbiology, and other relevant scientific disciplines can apply. Freshers are eligible for these opportunities, with experience requirements ranging from 0–1 year to 0–2 years, depending on the position.

eAspire Technolabs Recruitment 2026 – Job Details

Positions Available at eAspire Technolabs

The company is hiring for the following positions:

1. Clinical Data Management Associate
2. Medical Writer
3. Pharmacovigilance Associate
4. Research Associate

1. Clinical Data Management Associate

Freshers Can Apply

Experience: 0–1 Year

Role Overview:

The Clinical Data Management Associate will support the collection, validation, processing, and management of clinical trial data. The role involves maintaining clinical research databases, identifying data discrepancies, and supporting clinical research teams.

Key Responsibilities:

• Collect, review, and manage clinical trial data from various sources.
• Enter and validate clinical study information in Electronic Data Capture (EDC) systems.
• Review Case Report Forms (CRFs) for accuracy and completeness.
• Identify missing, inconsistent, or incorrect data.
• Generate and manage data queries.
• Maintain clinical databases and ensure data integrity.
• Support database cleaning, reconciliation, and data validation.
• Coordinate with clinical research associates, investigators, and study teams.

Eligibility / Qualifications:

B.Pharm, M.Pharm, Pharm.D, Life Sciences, Biotechnology, Microbiology, or related disciplines.

Required Skills:

• Clinical data entry and validation
• Clinical trial documentation
• Case Report Forms (CRFs)
• Data cleaning and query management
• Basic knowledge of EDC systems
• MS Excel and MS Office

2. Medical Writer

Freshers Can Apply

Experience: 0–1 Year

Role Overview:

The Medical Writer will develop scientific and medical content for pharmaceutical, healthcare, and clinical research projects, ensuring scientific accuracy and compliance with industry standards.

Key Responsibilities:

• Develop scientific content, medical reports, and clinical research documents.
• Research medical literature, clinical studies, and scientific publications.
• Prepare clinical study reports, research manuscripts, and regulatory documentation.
• Convert complex medical information into clear and understandable content.
• Review and edit medical documents for accuracy, grammar, and consistency.
• Assist in preparing abstracts, literature reviews, and scientific presentations.

Eligibility / Qualifications:

B.Pharm, M.Pharm, Pharm.D, Life Sciences, Biotechnology, Microbiology, or related disciplines.

Required Skills:

• Scientific and medical content writing
• Medical literature research
• Technical writing and documentation
• Editing and proofreading
• Knowledge of clinical research
• Medical terminology and pharmaceutical concepts

3. Pharmacovigilance Associate

Freshers Eligible

Experience: Freshers / 0–2 Years

Role Overview:

The Pharmacovigilance Associate will support drug safety monitoring through the collection, assessment, documentation, and reporting of adverse drug reactions (ADRs) and adverse events (AEs).

Key Responsibilities:

• Collect, review, and process ADR and AE reports.
• Monitor drug safety information from clinical trials and post-marketing surveillance.
• Perform Individual Case Safety Report (ICSR) processing and data entry.
• Review medical records and safety reports for accuracy and completeness.
• Identify and report potential safety concerns related to pharmaceutical products.
• Maintain pharmacovigilance databases and safety documentation.

Eligibility / Qualifications:

B.Pharm, M.Pharm, Pharm.D, Life Sciences, Biotechnology, or related fields.

Required Skills:

• Basic understanding of pharmacology and drug safety
• Adverse Drug Reaction (ADR) reporting
• Individual Case Safety Report (ICSR) processing
• Knowledge of MedDRA terminology
• Pharmacovigilance databases and safety reporting tools
• Clinical trial documentation
• Understanding of regulatory guidelines

4. Research Associate

Freshers Can Apply

Experience: 0–1 Year

Role Overview:

The Research Associate will support pharmaceutical and biotechnology research activities, including laboratory experiments, formulation development, product testing, data analysis, and research documentation.

Key Responsibilities:

• Conduct laboratory experiments and scientific investigations.
• Assist in R&D activities, including formulation development and product testing.
• Perform literature reviews and gather scientific information.
• Prepare experimental protocols, research reports, and technical documentation.
• Collect, record, analyze, and interpret laboratory data.
• Support pharmaceutical formulation development and process optimization.
• Operate laboratory instruments and equipment.
• Maintain laboratory records and experimental observations.

Eligibility / Qualifications:

B.Pharm, M.Pharm, Pharm.D, Biotechnology, Biochemistry, Microbiology, Chemistry, Life Sciences, or related disciplines.

Required Skills:

• Research and experimental techniques
• Laboratory operations and scientific testing
• Data collection and analysis
• Scientific literature review
• Research documentation and report writing
• Basic knowledge of pharmaceutical formulations and drug development

Educational Qualifications – Who Can Apply?

Candidates from the following educational backgrounds are eligible for the respective positions:

Eligibility is based on the qualifications mentioned in the respective job descriptions.

Walk-in / Application Details

• Company: eAspire Technolabs Inc.
• Recruitment Posted By: Evoke HR
• Job Location: Ahmedabad, Gujarat
• Positions: Clinical Data Management Associate, Medical Writer, Pharmacovigilance Associate, Research Associate
• Employment Type: Full-Time