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Senior Clinical Project Administrator

Labcorp
Labcorp
0-3 years
upto 5 LPA
Bangalore, India
10 April 24, 2026
Job Description
Job Type: Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc. 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 Clinical Project Administrator

Location: Bangalore, Karnataka, India (On-site)
Company: Labcorp
Job ID: 2612578
Job Type: Full-Time
Work Model: Rotational Shift (5 Days Working)
Experience Required: 0–3 years (Freshers can apply; 3 years preferred)


About the Company

Labcorp is a global leader in diagnostic testing and drug development services, supporting healthcare providers, pharmaceutical companies, and researchers in advancing patient care. With a strong presence across clinical trials and laboratory services, Labcorp continues to drive innovation in global healthcare.


Job Overview

The Senior Clinical Project Administrator role is an entry-to-intermediate level opportunity designed for candidates looking to build a strong foundation in clinical research operations. This position focuses on project coordination, documentation management, quality compliance, and cross-functional collaboration within clinical trial support teams.


Key Responsibilities

  • Follow departmental Standard Operating Procedures (SOPs) and Work Instructions to ensure compliance

  • Complete all assigned training modules within defined timelines

  • Manage day-to-day operational tasks while maintaining quality and productivity standards

  • Handle project documentation and ensure proper version control and audit readiness

  • Provide administrative and technical support to internal clinical teams

  • Conduct quality checks to ensure accuracy and compliance of deliverables

  • Escalate issues proactively and ensure timely resolution

  • Track, analyze, and report project metrics as per management requirements

  • Support implementation of updated processes, SOPs, and workflow improvements

  • Participate in knowledge-sharing sessions and cross-functional team discussions

  • Assist in workload planning and project allocation based on priorities

  • Identify process gaps and recommend improvements to enhance quality compliance

  • Support training initiatives, including preparation of training materials and agendas

  • Mentor junior team members and support competency development post-training

  • Ensure team training records are maintained, compliant, and audit-ready


Minimum Qualifications

  • Bachelor’s Degree in Life Sciences or related field


Preferred Qualifications

  • 0–3 years of experience in clinical research, clinical operations, or project support roles

  • Master’s Degree in Life Sciences (preferred but not mandatory)


Required Skills and Competencies

  • Strong organizational and time management skills

  • High attention to detail and quality-focused mindset

  • Effective communication and interpersonal abilities

  • Ability to manage multiple tasks in a fast-paced clinical environment

  • Proficiency in computer systems and clinical research tools

  • Problem-solving mindset with proactive approach to challenges


Work Environment and Growth Opportunities

  • Exposure to global clinical trial operations and project workflows

  • Opportunity to work with cross-functional teams in a leading CRO environment

  • Strong learning and development ecosystem with structured training programs

  • Career progression opportunities into Clinical Project Management and advanced research roles


Diversity and Inclusion Commitment

Labcorp is an equal opportunity employer committed to fostering an inclusive and diverse workforce. Employment decisions are based on merit, qualifications, and business needs, ensuring fair and unbiased opportunities for all applicants.


Important Note for Applicants

This role is suitable for both freshers and candidates with up to 3 years of experience in clinical research or related domains. Candidates with strong foundational knowledge and willingness to learn are highly encouraged to apply.


How to Apply

Apply through the official careers portal of the company or explore verified global opportunities on ThePharmaDaily.com to accelerate your clinical research career.