Medical or Life Sciences Data Curator  

About Expedock

We are a tech-enabled workforce augmentation platform leveraging top 1% offshore talent & cutting edge technology to enable businesses to unlock their full potential.

Role Overview:

We’re hiring a Medical / Life Sciences Data Curator to review and summarize clinical trials, publications, and regulatory updates for weekly reports. Ideal candidates have backgrounds in pharmacy, clinical research, pharmacovigilance, regulatory affairs, medical writing, or related life sciences fields. Responsibilities include applying inclusion/exclusion criteria, verifying sources, and producing concise, structured summaries.

Key Responsibilities:

You will review source materials such as:

• Clinical trial registry updates
• Pharma / biotech press releases
• Medical or scientific publications
• Conference abstracts
• Regulatory updates
• Patent updates
• Company pipeline or asset updates
• Medical affairs or drug safety updates
• Product, indication, or development milestone announcements

For each source item, you will:

• Determine whether the item should be included in a weekly monitoring report
• Apply clear inclusion / exclusion criteria
• Identify the relevant company, product, asset, indication, mechanism of action, study, or update
• Summarize the key information in concise, source-grounded language
• Verify claims against the original source
• Flag ambiguity, missing information, or uncertain relevance
• Maintain structured data in a consistent format
• Perform quality checks for accuracy, completeness, and clarity

A typical task may involve reviewing a clinical trial update and identifying:

• Trial title and registry
• Sponsor
• Phase
• Indication
• Asset or treatment being studied
• What changed since the prior update
• Whether the change is meaningful
• Whether it should be included in the weekly monitor
• A short summary of the update
• The source link or citation

Another task may involve reviewing a press release and determining whether it contains a meaningful clinical, regulatory, publication, pipeline, or corporate update that should be captured.

Why Expedock:

• Supportive Remote Environment: Work from home alongside a collaborative team that values growth and mutual success.
• Seamless Onboarding & Training: Get up to speed quickly with a structured program and client specific training designed to make you a subject matter expert in your assigned workflows.

Candidate Data & Privacy Notice

By submitting your application to Expedock, you acknowledge and consent to the collection, use, and processing of your personal information for recruitment and hiring purposes. Your information will be used to:

• Evaluate your qualifications and suitability for current and future roles
• Communicate with you throughout the recruitment process Improve our hiring processes and overall candidate experience
• Maintain talent pools for future opportunities, where permitted by law

We handle candidate data with care and in accordance with applicable data protection and privacy regulations. Your information will only be accessed by authorized team members and will not be shared with third parties without your consent, unless required by law.

Required Qualifications:

• Strong attention to detail
• Ability to read and understand medical / scientific materials
• Clear written English
• Ability to summarize complex information concisely
• Comfort working with structured templates or spreadsheets
• Ability to follow detailed rules and criteria
• Strong source-verification habits
• Ability to distinguish material updates from non-relevant information
• Comfort asking clarifying questions when source information is incomplete
• Reliability and consistency in repeated review task

Preferred Qualifications:

• Experience with ClinicalTrials gov
• Experience with PubMed or scientific publications
• Experience in pharmacovigilance or regulatory affairs
• Experience in medical writing or clinical document QC
• Experience with clinical trial management systems or clinical data systems
• Familiarity with pharma / biotech pipelines
• Familiarity with oncology, immunology, rare disease, or other therapeutic areas
• Experience in data annotation, data curation, or human evaluation work
• Experience using AI tools for research support, while still verifying outputs against primary sources