[Hiring] Clinical Research Scientist @Lumos Pharma

Role Description

The Clinical Research Scientist plays a critical role in Clinical Development supporting clinical research programs including data collection and analysis, data management, and preparation of Clinical Study Reports (CSRs). This position is responsible for ensuring high-quality data is collected and managed in alignment with regulatory standards, and for contributing to the scientific analysis and interpretation of study results.

• Collaborates closely with cross-functional teams, including clinical operations, regulatory, biostatistics, and medical writing, to ensure successful and compliant execution of clinical trials.
• Supports leadership teams in special projects supporting business development.
• Contributes to protocol synopses, clinical development plans, and evidence strategies that align endpoints with patient-relevant outcomes and regulatory expectations.

Qualifications

• Advanced degree in life sciences, pharmacy, or a related field (e.g., PharmD, PhD, NP, or master’s in clinical research).
• 3+ years of experience in clinical research or a related field. Experience in a sponsor or biotech environment preferred; rare disease experience is a plus.
• Proficient in tools to evaluate and present data including Word, Excel and PowerPoint.
• Solid understanding of Good Clinical Practice (GCP) and International Council for Harmonisation (ICH) guidance, including E6 Revision 3 and E9, as well as familiarity with Title 21 of the Code of Federal Regulations (CFR) Part 11 and General Data Protection Regulation (GDPR) requirements for clinical data.
• Ability to interpret Statistical Analysis Plans (SAPs) and tables, listings, and figures (TLF) templates, and work effectively with statisticians and programmers.

Requirements

• Strong knowledge of data collection and management practices.
• Demonstrated CRF design and edit check specification experience.
• Familiarity with Clinical Study Report (CSR) templates, guidelines, and regulatory requirements.
• Strong analytical and organizational skills, attention to detail and commitment to data integrity.
• Comfort communicating complex results to technical and non-technical audiences.
• Ability to work collaboratively across multiple functions and manage complex projects.
• Prior experience in endocrinology. Experience with pediatric populations, growth endpoints, or hormone biomarker strategies is a plus.

Benefits

• Industry-competitive compensation
• Generous health and welfare benefits, including company-paid dental and vision benefits with dependents coverage, short-term and long-term disability, and basic life insurance.
• Lumos covers 95 – 85% of medical premium
• Health Reimbursement Arrangement
• 8 weeks of fully paid parental leave for all new parents
• Gym or fitness class reimbursement
• 401(k) with 5% employer contribution
• Flexible work hours and location
• Generous PTO policy
• 11 paid holidays in the US
• Offices in Austin, TX and Ames, IA