Clinical Scientist

OCUGEN OPCO INC; Malvern (Chester County); On-site; USD 120,000 - 160,000; Full time

Job summary

OCUGEN OPCO INC is seeking a Clinical Scientist to support clinical development programs through data-driven insights, analysis, and high-impact visual communication. This role focuses on retina development and trials data analysis, parsing and interpreting clinical trial data, and generating figures and presentations for study execution and development strategy.

The candidate will collaborate with Biostatistics, Data Management, and Clinical Operations to ensure data quality and usability,

Qualifications

• Advanced degree in life sciences (PhD, PharmD, MD) preferred.
• Minimum of 5 years of experience in clinical development, clinical data analysis, programming, DSMB or DMC support or related analytics roles.
• Proficiency in programming languages such as SAS, R, Python, SQL, or similar tools.
• Demonstrated ability to generate high-quality visualizations, tables, and presentations from clinical datasets.
• Experience with Data Visualization tools (R-Shiny, Power BI, Tableau or AI based tools) is a plus.
• Working knowledge of clinical trial design, operations, GCP, and clinical data structures.
• Strong analytical thinking, attention to detail, and communication skills, with the ability to convey complex data clearly.
• Expertise in Ophthalmology and Neuroscience is preferred.

Responsibilities

• Maintains a strong understanding of the therapeutic disease areas and drug candidates, including disease biology and competitive landscape.
• Proposes, designs, and executes clinical research studies across assets; develops evidence-based development strategies.
• Analyzes study objectives and design and identifies data quality issues with mitigation strategies.
• Collaborates with Biostatistics, Data Management, Clinical Operations, and vendors for data cleaning, reconciliation, and quality oversight.
• Contributes to protocols, SAP support materials, CSRs, DSURs and interim analyses.
• Develops clear, concise, and visually compelling scientific materials for leadership and study teams.
• Reviews safety, efficacy, and operational data to identify meaningful findings and inform decisions.
• Synthesizes complex clinical data into actionable recommendations for cross-functional leadership.

Skills

SAS

R

Python

SQL

Data visualization

Communication skills

Clinical data analysis

Education

Advanced degree in life sciences

Tools

R-Shiny

Power BI

Tableau

Job description

Job Details: Job Location: Main Corporate Office - Malvern, PA 19355, Position Summary

The clinical scientist will support clinical development programs through data-driven insights, analysis, and high-impact visual communication. This role is responsible for retina development and trials data analysis, parsing and interpreting clinical trial data, generating figures and presentations, and supporting data review activities to inform study execution and development strategy.

The individual will work closely with Biostatistics, Data Management, and Clinical Operations to ensure data quality, consistency, and usability. Success in this role requires strong programming and data visualization skills, along with the ability to translate complex clinical data into clear, actionable insights for both internal and external stakeholders.

Responsibilities

• Maintains a strong understanding of the therapeutic disease area(s) and drug candidates, including underlying disease biology, clinical manifestations, mechanism of action, and the evolving competitive landscape.
• Applies scientific and clinical expertise to propose, design, and execute clinical research and development studies across early- and late-stage assets; develops and communicates evidence-based clinical development strategies grounded in relevant scientific literature.
• Demonstrates strong analytical understanding of clinical study objectives and design, including their implications for data analysis and interpretation; proactively identifies potential risks, trends, anomalies, and data quality issues and develops appropriate mitigation strategies.
• Collaborates cross-functionally with Biostatistics, Data Management, Clinical Operations, and external vendors to support data cleaning, reconciliation, tracking, and quality oversight, including laboratory, imaging, and other clinical data.
• Contributes to key clinical study documents and deliverables, including protocols, statistical analysis plan (SAP) support materials, clinical study reports (CSRs), DSURs and interim analyses.
• Develops clear, concise, and visually compelling scientific and clinical materials tailored to senior leadership, study teams, investigators, and governance forums.
• Performs ongoing review of emerging safety, efficacy, and operational data to identify meaningful findings and support timely study and program decisions.
• Synthesizes and communicates complex clinical data and scientific insights in a clear, structured, and clinically relevant manner, providing actionable recommendations to support cross-functional and leadership decision-making.

Qualifications:

• Advanced degree preferred in life sciences (i.e., PhD, PharmD, MD), quantitative sciences, or related field.
• Minimum of 5 years of experience in clinical development, clinical data analysis, programming, DSMB or DMC support or related analytics roles.
• Proficiency in programming languages such as SAS, R, Python, SQL, or similar tools.
• Demonstrated ability to generate high-quality visualizations, tables, and presentations from clinical datasets.
• Experience with Data Visualization tools (R-Shiny, Power BI, Tableau or AI based tools) is a plus.
• Working knowledge of clinical trial design, operations, GCP, and clinical data structures.
• Strong analytical thinking, attention to detail, and communication skills, with the ability to convey complex data clearly.
• Expertise in Ophthalmology and Neuroscience is preferred.

Working Conditions

This position is based in an office setting and requires in-person presence. Job may additionally require incumbent to be available outside of these hours to handle priority business needs. Approximately 10% travel may be required.

Ocugen is an equal opportunity employer. In order to provide equal employment and advancement opportunities to all individuals, we make all of our employment decisions based upon merit, qualifications, abilities, and an individual’s conduct and performance. We will not make any of our decisions, and will not discriminate against any employee or applicant, on the basis of race, color, religion, creed, national origin or ancestry, ethnicity, sex (including pregnancy), gender (including sexual orientation, gender identity and status as a transgender or transsexual individual), age, physical or mental disability, citizenship, past, current or prospective service in the uniformed services, genetic information, or any other characteristic protected from discrimination under the law. Ocugen complies with applicable federal, state and local laws governing nondiscrimination in employment.