Senior Specialist, Global Partnerships & Trial Optimization

By Admin · Clinical Research & Clinical Operations

HYDERABAD (IN)HYBRIDPOSTED: 9/13/2026
PHARMAFull-time
HIRING ORGANIZATIONREGENERONBiopharmaceuticals
Regeneron

ROLE OVERVIEW

Support global clinical trial optimization through feasibility analysis, enrollment planning, patient recruitment strategy, data analytics, KPI reporting, and technology-enabled solutions across Regeneron's Global Development organization.

ROLE DEFINITION & RESPONSIBILITIES

  • •Support feasibility, enrollment planning, and patient recruitment strategy activities
  • •act as technical and functional liaison for GPTO stakeholders
  • •perform data entry, transformation, analysis, and reporting
  • •maintain dashboards, KPIs, metrics, and vendor performance reports
  • •track portfolio and pipeline activities for resource planning
  • •develop technology-driven solutions and data systems
  • •create scalable processes, tools, templates, and training materials
  • •identify improvements to feasibility methodologies and data sources while maintaining ICH-GCP and SOP compliance.
Reporting Hierarchy: Works within Regeneron's Global Clinical Trial Services/Global Partnerships & Trial Optimization function and collaborates with Global Development teams, supporting functions, vendors, and senior leadership.

* Role responsibilities and qualifications synthesized based on industry benchmark standards.

QUALIFICATIONS & REQUIREMENTS

REQUIRED QUALIFICATIONS

  • Bachelor's degree in Life Sciences, Clinical Research, Data Analytics, Business, Healthcare, or related field
  • Bachelor's degree with 5+ years relevant experience or Master's degree with 3+ years relevant experience
  • 3+ years using databases and systems for clinical or operational data
  • proficiency in SQL and complex data sources
  • 2+ years with Power BI, Power Query, data visualization and analytical reporting
  • knowledge of clinical development, feasibility, recruitment and enrollment planning
  • awareness of ICH-GCP and clinical research standards
  • willingness to travel up to 10%.

PREFERRED QUALIFICATIONS

  • •Experience with Tableau
  • •Excel VBA expertise
  • •advanced data visualization skills
  • •experience developing technology-enabled clinical operations solutions.

REQUIRED VERIFIED SKILLS

SQL
Power BI
Power Query
Microsoft Excel
PowerPoint
Word
clinical data analysis
operational data reporting
data visualization
clinical trial feasibility
enrollment planning
patient recruitment
KPI reporting
database management
ICH-GCP
clinical research standards
stakeholder management

COMPENSATION & REWARDS

Salary: Competitive / Disclosed upon candidate shortlisting
Benefits: Competitive and comprehensive total rewards may include annual bonuses or incentive plans, equity awards, retirement benefits, health and wellness programs, insurance, paid time off, and family support benefits, depending on country and role.
Salary range is not explicitly disclosed in the posting. Regeneron states that compensation is determined based on country, role level, skills, and experience, with applicable total rewards potentially including bonuses, equity, retirement and health benefits.

ORGANIZATION CONTEXT & CULTURE

Regeneron is a biotechnology company focused on discovering, developing, and commercializing medicines for people with serious diseases through science and innovation.

TEAM SIZE: Large multinational biotechnology company
INDUSTRY: Biopharmaceuticals
Culture: Science-driven, collaborative, inclusive, innovative, data-driven, and focused on continuous improvement and patient impact.

EXPECTED CAREER ROADMAP

Can progress into senior clinical operations analytics, trial optimization leadership, clinical data strategy, feasibility and recruitment strategy, or broader Global Development program leadership roles.

APPLICATION ADVISORY

Highlight SQL, Power BI, Power Query, clinical data analytics, feasibility, enrollment planning, patient recruitment, KPI dashboards, and ICH-GCP knowledge. Demonstrate examples of improving operational efficiency through data-driven or technology-enabled solutions.

READY TO SUBMIT?

Verify your capability profile and matching credentials before submitting direct applications.