Why This Role Stands Out
This hybrid LIMS Business Analyst role offers an exciting opportunity to lead independent projects and drive impactful IT solutions within a leading biopharma company. You will thrive if you possess strong business analysis skills combined with an understanding of scientific environments, enabling you to translate complex needs into actionable strategies. This position is perfect for a self-motivated professional eager to take ownership and contribute to critical research IT initiatives.
Quick Overview
Job Description
What the hiring manager is looking for:
A senior-level BA who can lead projects independently, take initiative, and drive work with minimal oversight. The manager wants someone she can assign a project to and trust to own it from start to finish.
The emphasis is on strong Business Analyst experience, not just scientific credentials.
Experience supporting Research IT in a business-facing role is strongly preferred.
Someone with a blend of science/LIMS knowledge and solid BA skills would be ideal.
A PhD is a nice-to-have, but it is not required.
The manager is placing less emphasis on formal education and pure lab/scientific experience, as many vendors have submitted scientists with little or no BA or IT experience. She is looking for someone with proven Business Analyst expertise who also understands the scientific environment.
Position Overview:
We are seeking a skilled Scientific Business Analyst to join our client's Research IT team at a leading biopharma company. The ideal candidate will have experience working with Laboratory Information Management Systems (LIMS) within the Clinical and Preclinical Sample Management space and be well-versed in regulatory compliance as it relates to LIMS implementations. This role requires an independent, self-motivated professional capable of translating complex scientific and regulatory requirements into actionable IT solutions that align with business objectives.
Key Responsibilities:
Collaborate with cross-functional teams, including scientists, researchers, and IT professionals, to gather, analyze, and document business requirements for LIMS implementation and optimization.
Provide expert-level support in Clinical and Preclinical Sample Management, ensuring LIMS configurations meet scientific, operational, and regulatory needs.
Ensure compliance with relevant regulatory standards (e.g., FDA, EMA) throughout LIMS implementation, including data integrity, security, and validation requirements.
Conduct process analysis and provide recommendations for improving workflows related to sample management, data handling, and reporting.
Act as a liaison between business stakeholders and technical teams, facilitating clear communication to ensure successful project delivery.
Independently manage project deliverables, timelines, and documentation, while driving progress toward key milestones.
Key Qualifications:
Strong familiarity with LIMS platforms in the Clinical and Preclinical Sample Management space.
In-depth understanding of regulatory compliance, especially in the context of LIMS and biopharma research environments.
Proven ability to work independently, manage multiple priorities, and deliver high-quality results in a fast-paced environment.
Excellent analytical, problem-solving, and communication skills with the ability to work collaboratively with both technical and non-technical stakeholders.
Bachelor's degree in Life Sciences, Information Technology, or a related field; advanced degree preferred.
Preferred Experience:
Experience in a Research IT setting within the biopharma industry.
Knowledge of system validation and data integrity best practices for research and clinical environments.
Skill(s) and Description: Pharma, Formulation, Scientific Business Analysis, LIMS (Labware), ELN (IDBS), Jira, Agile, Lucid, Change Management, Research IT, Leadership
Extensive expertise in Formulation/Preclinical Development domain, a solid understanding of lab informatics (specifically, labware LIMS), familiarity with Jira and Agile methodologies, knowledge of Regulatory Submission standards, and strong change management abilities to lead the roll out and adoption of new technological solutions.
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