Research Ops Intern- Clinical Data

1 day ago

Coimbatore, Tamil Nadu, India Triomics Full time ₹ 6,00,000 - ₹ 8,00,000 per year

We are seeking a highly motivated and detail-oriented Research Ops Intern- Clinical Data to join our dynamic team. The ideal candidate will have a strong background in oncology, the ability to understand and interpret medical terminology from Electronic Health Records (EHR) and medical reports, and the expertise to extract and analyze data from patient notes. The candidate must have a background of clinical research and is able to comprehend clinical trials. Also have good knowledge about patient pre-screening, enrolling participants in oncology clinical trials . The role requires proficiency in Google Sheets and Excel, along with the ability to correlate medical data to meet specific requirements.

Duration: 3 months

Key Responsibilities:

Clinical Trials Acumen: Interpret the Inclusion and Exclusion criteria outlined in the clinical trials on and in study protocols, and use this information to assess patient eligibility for clinical trials.

Data Extraction and Curation: Extract relevant data from patient notes, EHRs, patient information, medical history, laboratory/pathology results, diagnoses, and treatments, to support oncology research and clinical decision-making.

Medical Terminology: Interpret and understand complex medical terms, especially those related to oncology to ensure accurate data extraction and analysis.

Data Management: Maintain and manage datasets using Google Sheets and Excel, ensuring data accuracy and integrity.

Correlation and Interpretation: Analyze medical data to identify patterns and correlations that align with project requirements.

Quality Assurance: Conduct regular quality checks and validation of extracted data to ensure consistency and accuracy.

Patients Pre-screening: Knowledge of pre-screening patients before enrolling to clinical trials would be required to curate and verify clinical trials on the companys platform

Qualifications:

Bachelors/Masters degree in a relevant field such as Clinical Research, Health Information Management, Medical Informatics, Oncology, or a related discipline.

6 months of experience in clinical research/oncology research/clinical data abstraction/clinical data curation. Candidates with Clinical Trial Certification will be preferred.

Proficiency in Google Sheets and Excel; familiarity with data extraction tools and EHR systems.

Strong understanding of oncology, medical, and pathology terminologies.

Excellent analytical and problem-solving abilities, with a keen eye for detail.

Strong written and verbal communication skills, with the ability to present complex data in a clear and concise manner.

Ability to manage multiple tasks and projects simultaneously, with strong organizational and time-management skills.

Ability to work effectively both independently and as part of a multidisciplinary team."

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