Biopharma Researcher and Data Entry (Reopen for additional hire)
Support Shepherd, Philippines
Job Description
Position : Data Entry
Work Hours (Client) : 8am to 5pm PST | M - F
Work Hours (MNL) : 12am to 9am PST | M - F
Holidays : PH regular and special holidays
Pay Range : $800-$1500/month (depending on interview assessment and client's approval) Please take note that pay will be given in USD
Incentive : This role will have a quota in a given week (TBD with the client) and incentives will be provided for exceeding the quota to reward high-quality work and efficiency
Company/Client Overview:
Company is a Los Angeles-based intelligence platform that helps biopharma companies amp; investors make better decisions by automating manual processes and allowing them to run novel analyses. Today, biotech analysis is a cumbersome, limited and error-prone process despite significant investment hinging on their output. Sleuth will be building the infrastructure upon which more rigorous analyses amp; data aggregation will be built, changing the way that diligence amp; research is done in the bioeconomy.
Duties and Responsibilities:
- Data Entry:
- Enter and update clinical trial information into designated templates / spreadsheets.
- Ensure accuracy and completeness of data, adhering to established standards and guidelines.
Research:
- Conduct thorough desktop research to gather relevant information
- Leverage public amp; proprietary resources, including clinicaltrials.gov, PubMed, PDF reports and databases
Quality Assurance:
- Perform quality checks on entered data to identify and correct any discrepancies.
- Collaborate with cross-functional teams to ensure data integrity and consistency
Requirements
Minimum Requirements:
- Bachelor's degree in a relevant field (e.g., life sciences, data management, information technology) would be a plus
- Virtual Assistant, Admin Assistant, or Data Analyst experience is acceptable as long as with data entry experience
- Experience in data entry or a related role, preferably within the biopharma or healthcare industry is a plus
- Familiarity with clinical trial processes and terminology is a plus
- Strong research skills and the ability to extract information from scientific publications.
- Detail-oriented with excellent organizational and time-management skills.
- Proficiency in using data entry tools and software (i.e. Google Sheets, Excel, Slack, Zoom, Adobe, etc.).
- Ability to set up basic VPN to setup location in the US would be helpful
- Above Average English Communication Skills