CPMS Intern

Summary

Join Allucent™ as a Clinical Pharmacology, Modeling & Simulation (CPMS) Intern and contribute to bringing life-changing therapies to patients globally. This 3-month summer internship (June-August 2025) offers a hybrid/remote work option. You will assist with various clinical pharmacology activities, including technical writing, PK analysis, and participation in internal initiatives. The role involves preparing and reviewing clinical documents, advising clients, conducting literature reviews, and developing templates and guidelines. Successful candidates will possess a Bachelor's degree, be pursuing an advanced scientific degree, and demonstrate strong analytical and communication skills. Allucent offers a comprehensive benefits package, including competitive salaries, professional development opportunities, flexible working hours, and a supportive work environment.

Requirements

• Bachelor’s degree
• Pursuing an advanced scientific degree (e.g., PharmD)
• Interest in career in industry and/or drug development research
• Demonstrates critical thinking and analytical skills
• Strong written and verbal communication skills including good command of English language
• Effective planning and organization skills
• Proficiency with various computer applications e.g. MS Office

Responsibilities

• Assists in the preparation and review of marketing blogs, clinical protocols, clinical study reports, clinical pharmacology strategic plans, INDs, clinical pharmacology and safety sections of NDAs, Investigator Brochures, FDA briefing packages, and other clinical and regulatory documents
• Assists with development of strategic advice to clients on clinical pharmacology and overall drug development activities as part of a cross functional team
• Performs literature searches and literature reviews, as assigned
• Leads the development of templates and guidelines for clinical pharmacology, regulatory and other written deliverables
• Seeks professional development opportunities to maintain knowledge of clinical pharmacology, regulatory requirements, and industry best practices
• Maintains up-to-date training on appropriate company SOPs, and familiarize with relevant PK and clinical pharmacology guidances
• Contribute to development of best practices and standard operating procedures for clinical pharmacology

Benefits

• Comprehensive benefits package per location
• Competitive salaries per location
• Departmental Study/Training Budget for furthering professional development
• Flexible Working hours (within reason)
• Opportunity for remote/hybrid* working depending on location
• Leadership and mentoring opportunities
• Participation in our enriching Buddy Program as a new or existing employee
• Internal growth opportunities and career progression
• Financially rewarding internal employee referral program
• Access to online soft-skills and technical training via GoodHabitz and internal platforms
• Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects
• Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees