Clinical Research Analyst

Straive; India; On-site; INR 450,000 - 750,000; Full time

Job summary

Straive in India is seeking a dedicated Data Reviewer to analyze and classify pharmaceutical information from automated feeds and manual pipelines, strictly following SOPs and organizational procedures.

The role requires a Life Sciences-based degree and 1+ year in secondary research or related analytical roles, with strong English communication and proficiency in MS Office. You will collaborate with a global team to ensure data quality and timely delivery.

Qualifications

• Must hold Life Sciences, Pharmacy, Medical Sciences, or related degree.
• Minimum 1+ year experience in secondary research, data entry, data curation, or related analytical roles.
• Strong English written and verbal communication.
• Proficient in MS Office (Word, Excel, Outlook, Teams, PowerPoint).

Responsibilities

• Analyze and classify complex pharma information from automated feeds and manual data pipelines.
• Conduct comprehensive secondary research using credible industry sources to validate data.
• Ensure data quality, timeliness, and adherence to SOPs in all tasks.
• Collaborate with peers to discuss findings and resolve discrepancies.

Skills

Data review

Secondary research

Quality assurance

SOP adherence

Team collaboration

Professional development

English communication

Education

Life Sciences degree

Postgraduate/Doctorate preferred

Job description

Required Qualifications & Competencies

• Data Review & Classification: Independently analyze, categorize, and classify complex pharmaceutical information derived from both automated technology feeds and manual data pipelines, strictly following established organizational procedures.
• Secondary Research & Validation: Conduct comprehensive secondary research utilizing highly credible, authoritative industry sources to cross-reference, verify, and validate all ingested data points for accuracy.
• Quality & Timeliness Assurance: Take complete ownership of your workflow to consistently meet and maintain exceptionally high standards of data quality, meticulous accuracy, and operational timeliness in all assigned tasks.
• SOP Adherence & Escalation: Rigorously follow detailed internal process documentation and Standard Operating Procedures (SOPs), while demonstrating the analytical judgment necessary to elevate complex discrepancies or systemic issues to senior team members when required.
• Professional Development: Proactively participate in continuous training modules to systematically develop your foundational pharmaceutical industry knowledge and master specialized data classification skills.
• Team Collaboration: Work dynamically with your peer group to discuss findings, share insights, and collaboratively resolve any data or classification discrepancies.

Educational Background:

Must hold a Graduate, Post-Graduate, or Doctorate degree in Life Sciences, Pharmacy, Medical Sciences, or a closely related scientific field.

• Professional Experience: Minimum of 1+ years of experience in secondary research, data entry, data curation, or related analytical roles; equivalent commensurate skills and strong academic foundations will also be considered.
• Domain Vocabulary: A strong foundational understanding of global drug pipelines, product-related medical information, regulatory frameworks, and standard pharmaceutical terminology.
• Communication Skills: Must possess fluent written and verbal English communication skills to effectively collaborate within a global team environment.
• Technical Proficiency: Highly proficient with the core Microsoft Office suite, including practical everyday navigation of Word, Excel, Outlook, Teams, and PowerPoint.