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Senior Research Associate

1-5 years
Not Disclosed
10 Nov. 20, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Research Associate – Chemistry Solutions

Location: Hyderabad, India
Office Location: Mallapur, Hyderabad
Experience Required: 1 to 5 years in Organic or Medicinal Chemistry
Department: Chemistry Solutions
Employment Type: Full-Time
Salary Range: As per industry standards (Annual INR)


Role Overview

The Senior Research Associate will be responsible for independently executing chemical reactions and synthesizing target molecules or compounds in accordance with client specifications. This position requires strong expertise in organic synthesis, analytical techniques, and laboratory safety protocols. The role contributes directly to high-quality molecule development, data integrity, and timely project delivery within a fast-paced research environment.


Key Responsibilities

1. Reaction Setup and Synthesis Execution

  • Understand client requirements, synthetic routes, and project objectives.

  • Review and discuss MSDS (Material Safety Data Sheets) with the team.

  • Identify potential safety concerns and collaborate with the supervisor to mitigate risks.

  • Plan and execute chemical reactions using appropriate reagents, equipment, and controlled conditions.

  • Manage parallel reactions efficiently while maintaining accuracy and productivity.

  • Monitor reaction progress using standard analytical techniques.

  • Perform suitable workup and purification procedures to deliver intermediary or final compounds meeting required quality standards.

  • Analyze analytical data, interpret synthetic outcomes, and prepare accurate reports.

  • Meet productivity benchmarks in terms of reaction count, steps, purity, and timelines.

2. Laboratory Safety and Compliance

  • Follow Good Laboratory Practices (GLP), safety standards, and quality systems at all times.

  • Ensure proper use, maintenance, and calibration of laboratory equipment as per SOPs.

  • Maintain high standards of housekeeping and safety compliance in the laboratory.

3. Documentation and Data Integrity

  • Maintain accurate, compliant documentation of experiments and observations in laboratory notebooks.

  • Ensure complete data integrity and adherence to client-driven documentation requirements.

  • Uphold strict IP confidentiality and comply with all relevant policies.

  • Prepare final reports and contribute to project documentation as required.

4. Continuous Learning and Skill Enhancement

  • Strengthen knowledge in organic synthesis, analytical methods, and safety protocols.

  • Participate in technical discussions, project training sessions, and ongoing skill development programs.

  • Collaborate with supervisors to enhance scientific capabilities and performance.


Functional and Technical Skills Required

  • Strong understanding of Organic and Medicinal Chemistry principles.

  • Proficiency in executing synthetic reactions and handling laboratory equipment.

  • Knowledge of safety protocols, GLP, and MSDS compliance.

  • Familiarity with purification methods and analytical characterization.

  • Understanding of IP confidentiality policies and data integrity standards.

  • Ability to optimize resources and perform cost-benefit evaluations.


Educational Qualifications

  • MSc in Organic Chemistry or Medicinal Chemistry

  • Experience Required: 1 to 5 years of relevant industry experience.

  • Candidates with research publications in reputed scientific journals will be preferred.


Additional Information

  • Reporting Structure: To be aligned with departmental guidelines.

  • Industry: Chemical Research, Pharmaceutical R&D, CRO/CRAMS.

  • KPIs: Reaction productivity, quality of synthesized compounds, documentation accuracy, adherence to safety standards, and project timelines.

  • Work Environment: Laboratory-based role with strict compliance to safety procedures.

  • Travel Requirements: Limited or project-specific, if applicable.