PHARMAFull-time
Laboratory Report Processor I -BSC in Medical Laboratory Technology
By Admin · Research & Development (Lab & Science)
BANGALORE (IN)ONSITEPOSTED: 9/1/2026
PHARMAFull-time
HIRING ORGANIZATIONICONContract Research Organization (CRO) / Clinical Research / Healthcare Services
ROLE DEFINITION & RESPONSIBILITIES
Position Summary
Process and manage laboratory reports for clinical research studies, ensuring timely and accurate communication of results.
Take responsibility for clinical laboratory operations deliverables while maintaining quality, accuracy, and operational efficiency.
Core Responsibilities
Process laboratory reports with accurate data entry and formatting in accordance with established protocols and quality standards.
Review laboratory reports for completeness and accuracy before final distribution to relevant stakeholders.
Collaborate with laboratory staff to collect required information and resolve discrepancies identified in report content.
Maintain organized records of report submissions and track report status throughout the processing workflow.
Conduct timely follow-up on outstanding reports or actions to support delivery timelines.
Assist with continuous improvement of laboratory report-processing procedures to enhance operational efficiency and quality.
Qualifications & Experience
Bachelor's degree in Medical Laboratory Technology or a relevant field such as Life Sciences, Laboratory Technology, or Business Administration.
Requires 2-3 years of experience in report processing, data management, or a related role, preferably in a laboratory or clinical research environment.
Strong attention to detail and organizational skills.
Ability to manage multiple tasks and deadlines effectively.
Good communication skills and a collaborative approach to working with team members and stakeholders.
Proficiency in Microsoft Office Suite.
Familiarity with Laboratory Information Management Systems (LIMS) is an advantage.
Willingness to travel approximately 1% as required.
Employment is contingent upon having the legal right to work in India.
Quality & Operational Standards
Maintain accuracy and completeness of clinical laboratory reports.
Follow established protocols, report-processing procedures, and quality standards.
Ensure appropriate documentation and tracking of report submissions.
Identify and resolve discrepancies in collaboration with laboratory personnel.
Contribute to process improvements that support efficiency and quality in clinical laboratory operations.
Rewards & Benefits
Competitive base salary and performance-related incentives.
Health and wellbeing programs, including medical, dental, and vision coverage where applicable.
Retirement and pension plans.
Life assurance and disability coverage.
Employee assistance programs and wellbeing resources.
Learning and development opportunities through structured training and career pathways.
Benefits may vary depending on role and location.
Company & Inclusion
ICON is a global healthcare intelligence and clinical research organization focused on bringing new medicines and treatments to patients faster.
ICON emphasizes integrity, collaboration, agility, and inclusion in its working culture.
ICON is an equal opportunity employer committed to an inclusive and accessible workplace.
Reasonable accommodations are available during the recruitment process.
REQUIRED VERIFIED SKILLS
Bachelor's Degree
Medical Laboratory Technology
Life Sciences
Laboratory Technology
Report Processing
Data Management
Clinical Laboratory Operations
Microsoft Office
Attention to Detail
Organizational Skills
Quality Standards
Data Accuracy
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
The posting does not disclose a specific salary range or fixed compensation figures. It states that ICON provides a competitive total rewards package that may include base salary, performance-related incentives, health and wellbeing programs, retirement and pension plans, life assurance, disability coverage, employee assistance resources, and learning and development opportunities. Actual benefits vary by role and location, so candidates should confirm the Bangalore-specific compensation and benefits package during recruitment.
ORGANIZATION CONTEXT & CULTURE
ICON plc is a global provider of outsourced drug development and commercialization services to pharmaceutical, biotechnology, medical device, and government organizations. The company specializes in a broad range of clinical research services, from Phase I-IV studies to consulting and data solutions. ICON helps its clients accelerate the development of drugs and devices through comprehensive scientific and operational expertise.
TEAM SIZE: 41,100+ employees
INDUSTRY: Contract Research Organization (CRO) / Clinical Research / Healthcare Services
EXPECTED CAREER ROADMAP
This role provides an entry-to-mid-level pathway within clinical laboratory operations and clinical research data workflows. Experience gained in laboratory report processing, data management, quality review, stakeholder coordination, and LIMS can support progression into senior laboratory operations, clinical data management, laboratory data management, clinical research operations, quality-focused roles, or other specialized positions within a CRO environment. ICON also states that it provides structured learning, development opportunities, and career pathways, supporting longer-term professional growth.
APPLICATION ADVISORY
Highlight a Bachelor's degree in Medical Laboratory Technology, Life Sciences, Laboratory Technology, or another directly relevant field. Clearly demonstrate 2-3 years of laboratory report processing, data management, clinical research, or related experience. Emphasize accuracy, report review, data entry, formatting, discrepancy resolution, record tracking, deadline management, and quality compliance. Mention Microsoft Office proficiency and any LIMS exposure. Use resume examples showing how you identified and corrected data/report discrepancies, managed multiple deadlines, collaborated with laboratory teams, and improved processing efficiency. Be prepared to discuss attention to detail, quality-control practices, stakeholder communication, and clinical laboratory workflows.
RECOMMENDED TRAINING
1/5
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