Associate Study Coordinator (Bengaluru)

Associate Study Coordinator (Bengaluru)

02 Aug
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The Pharma Daily - Powered by Vigisolvo
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Bengaluru

02 Aug

The Pharma Daily - Powered by Vigisolvo

Bengaluru

Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Labelling Assessment, MedDRA Coding, mRS and EQ-5D-5L, Triage of ICSRs, WHO DD Coding Associate Study Coordinator – Labcorp Discover more Pharma Geographic Reference Dictionaries & Encyclopedias Job Details Job Title: Associate Study Coordinator

Company: Labcorp

Location: Bengaluru, India (Yeshwanthpur Office)

Job Type: Full-time

Work Mode: Office-based

Shift: 2:00 PM – 11:00 PM

Application Deadline: 27 July 2026

Experience Required: 1+ year of experience in a scientific, pharmaceutical, or CRO environment.

Estimated Salary Package (Market Standard): ₹4.5 – ₹7.5 LPA (may vary based on skills, experience, and company policies).

About The Company Discover more Career Resources & Planning Educational Resources Science data City & Local Guides Knowledge Management Labcorp is a global leader in laboratory services, supporting healthcare providers, researchers, pharmaceutical companies, and health systems with advanced diagnostics, scientific research, and data-driven healthcare solutions.

Key Responsibilities Conduct or support Noncompartmental Analysis (NCA) for Pharmacokinetic (PK) and Toxicokinetic (TK) studies.

Read and interpret study protocols, amendments, schedules, SOPs, and regulatory requirements.

Prepare, review, and maintain study documentation with accuracy and timely completion.

Support study finalization and archival activities while maintaining study schedules.

Perform study archival activities according to established procedures.

Prepare and edit technical documents to ensure high-quality deliverables.

Review tables and figures prepared by team members.

Assist in preparing study-related reports, tables, and figures.

Learn and use pharmacokinetic data collection and reporting systems effectively.

Coordinate study schedules with Study Directors, Principal Investigators, and laboratory teams.

Support additional study coordination tasks as assigned.

Required Qualifications Master's degree in Pharmacy, Life Sciences, or a related scientific field (or equivalent qualification).

Minimum 1 year of relevant experience in the pharmaceutical, scientific, or CRO industry.

Knowledge of Pharmacokinetics (PK) and Toxicokinetics (TK) is preferred.

Experience with Phoenix WinNonlin is an added advantage.





Proficiency in Microsoft Word, Excel, and Outlook.

Strong organizational and multitasking abilities.

Excellent written and verbal communication skills.

Ability to work effectively in a collaborative team environment.

Preferred Skills Pharmacokinetic (PK) and Toxicokinetic (TK) knowledge.

Noncompartmental Analysis (NCA).

Phoenix WinNonlin.

Documentation and technical writing.

Study coordination and scheduling.

Regulatory compliance and SOP understanding.

Microsoft Office Suite.

Time management and teamwork. One-Line Experience Candidates with 1+ year of experience in Pharmacokinetics (PK), Toxicokinetics (TK), study coordination, or CRO/pharmaceutical research environments are preferred.

Estimated Salary

Package (Market Standard) Expected CTC: ₹4.5 – ₹7.5 LPA

Freshers (Exceptional Profile): Around ₹4 – ₹5 LPA

Experienced (1–2 Years): Around ₹5.5 – ₹7.5 LPA Why Join Labcorp? Work with a globally recognized healthcare and laboratory services company.

Gain exposure to PK/TK studies and clinical research operations.

Opportunities for growth opportunities in the pharmaceutical and CRO industry.

Collaborative work environment with global teams.

Competitive compensation and employee benefits.

Application

Deadline 27 July 2026 Associate Study Coordinator – Labcorp Discover more Pharma Geographic Reference Dictionaries & Encyclopedias Job Details Job Title: Associate Study Coordinator

Company: Labcorp

Location: Bengaluru, India (Yeshwanthpur Office)

Job Type: Full-time

Work Mode: Office-based

Shift: 2:00 PM – 11:00 PM

Application Deadline: 27 July 2026

Experience Required: 1+ year of experience in a scientific, pharmaceutical, or CRO environment.

Estimated Salary Package (Market Standard): ₹4.5 – ₹7.5 LPA (may vary based on skills, experience, and company policies).

Key Responsibilities Conduct or support Noncompartmental Analysis (NCA) for Pharmacokinetic (PK) and Toxicokinetic (TK) studies.

Read and interpret study protocols, amendments, schedules, SOPs,



and regulatory requirements.

Prepare, review, and maintain study documentation with accuracy and timely completion.

Support study finalization and archival activities while maintaining study schedules.

Perform study archival activities according to established procedures.

Prepare and edit technical documents to ensure high-quality deliverables.

Review tables and figures prepared by team members.

Assist in preparing study-related reports, tables, and figures.

Learn and use pharmacokinetic data collection and reporting systems effectively.

Coordinate study schedules with Study Directors, Principal Investigators, and laboratory teams.

Support additional study coordination tasks as assigned.

Required Qualifications Master's degree in Pharmacy, Life Sciences, or a related scientific field (or equivalent qualification).

Minimum 1 year of relevant experience in the pharmaceutical, scientific, or CRO industry.

Knowledge of Pharmacokinetics (PK) and Toxicokinetics (TK) is preferred.

Experience with Phoenix WinNonlin is an added advantage.

Proficiency in Microsoft Word, Excel, and Outlook.

Strong organizational and multitasking abilities.

Excellent written and verbal communication skills.

Ability to work effectively in a collaborative team environment.

Preferred Skills Pharmacokinetic (PK) and Toxicokinetic (TK) knowledge.

Noncompartmental Analysis (NCA).

Phoenix WinNonlin.

Documentation and technical writing.

Study coordination and scheduling.

Regulatory compliance and SOP understanding.

Microsoft Office Suite.

Time management and teamwork. One-Line Experience Candidates with 1+ year of experience in Pharmacokinetics (PK), Toxicokinetics (TK), study coordination, or CRO/pharmaceutical research environments are preferred.

Estimated Salary

Package (Market Standard) Expected CTC: ₹4.5 – ₹7.5 LPA

Freshers (Exceptional Profile): Around ₹4 – ₹5 LPA

Experienced (1–2 Years): Around ₹5.5 – ₹7.5 LPA Why Join Labcorp? Work with a globally recognized healthcare and laboratory services company.

Gain exposure to PK/TK studies and clinical research operations.

Opportunities for career growth in the pharmaceutical and CRO industry.

Collaborative work environment with global teams.

Competitive compensation and employee benefits.

Application

Deadline 27 July 2026

📌 Associate Study Coordinator (Bengaluru)
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