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Clinical Project Associate

Labcorp
3+ years
INR 6-8 LPA
Bangalore, India
10 June 17, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, CPT, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, HCPCS Level II, ICD-10-CM, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICD-10-PCS, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing

Key Responsibilities

Project Coordination

  • Support clinical research projects and operational activities.

  • Manage project documentation and records.

  • Coordinate with internal departments for project-related tasks.

  • Ensure timely completion of assigned deliverables.

Quality Management

  • Perform quality checks on completed work.

  • Review peer deliverables for compliance and accuracy.

  • Identify process gaps and recommend improvements.

  • Ensure adherence to SOPs and Work Instructions.

Training & Mentorship

  • Train and mentor new team members.

  • Maintain training records and compliance documentation.

  • Track weekly and monthly training completion.

  • Conduct knowledge-sharing sessions.

Process Improvement

  • Assist with implementation of revised procedures.

  • Contribute to process optimization initiatives.

  • Participate in continuous improvement activities.

  • Support audit readiness and compliance efforts.

Documentation & Compliance

  • Create, update, and review SOPs and Work Instructions.

  • Ensure version-controlled documentation is maintained.

  • Support Quality Assurance requirements.

  • Maintain audit-ready documentation.

Workload Management

  • Assess project priorities and allocate work accordingly.

  • Monitor project timelines and workload distribution.

  • Escalate issues proactively and support timely resolution.


Required Skills

Technical Skills

  • Clinical Research Operations

  • Project Coordination

  • SOP Management

  • Quality Review

  • Documentation Management

  • Compliance & Audit Readiness

  • Training Coordination

Software Skills

  • Microsoft Excel

  • Microsoft Word

  • Microsoft PowerPoint

  • Microsoft Outlook

  • Clinical Trial Management Tools (preferred)

Soft Skills

  • Communication Skills

  • Leadership & Mentoring

  • Active Listening

  • Problem Solving

  • Organizational Skills

  • Time Management

  • Stakeholder Coordination


Preferred Knowledge

  • Clinical Trial Lifecycle

  • ICH-GCP Guidelines

  • Clinical Research Documentation

  • Regulatory Compliance

  • Quality Assurance Processes

  • Training Management

  • Clinical Operations