招聘
Benefits & Perks
•Commuter Benefits
•Company paid holidays
•Commuter
Required Skills
PK/PD principles
Population PK/PD Modeling
NONMEM
Monolix
Mixed-effects modeling
Covariate analysis
Exposure-response modeling
Survival analysis
R
Data handling
Data visualization
About the Role:
- This application is for a 6-month student role from July
- December 2026. Resume review begins in January 2026.
Clinical Pharmacology and Pharmacometrics (CPP) plays a central role in determining the right dose of the right molecule for the right patient by applying pharmacology principles, quantitative modeling, and simulations. CPP contributes across the entire drug‑development continuum—from pre‑R2D through regulatory submission, approval, and life‑cycle management. The function generates quantitative insight into what the body does to the drug (pharmacokinetics) and what the drug does to the body (pharmacodynamics), enabling prediction of benefit–risk, accelerating development, and informing regulatory strategy. CPP ultimately contributes to 25–40% of final drug‑label content.
This Co‑Op role will support Clinical Pharmacology strategy in a specific disease area by researching the competitive landscape, focusing on PK/PD relationship, and generating quantitative metrics to inform internal development. The role provides hands‑on exposure to industry drug development and clinical pharmacology strategy-setting.
What You’ll Do:
As a co-op, you will have the job as described below, but not limited to:
- Perform thorough literature search, data digitization, summary and visualization
- Produce or re-produce PopPK/PD models and/or statistical exposure – response models
- Perform meta-analysis or model-based based analysis (MBMA)
- Learn and implement the industry-standard data handling and modeling rules
- Support Clin Pharm Lead in summarizing the competitive landscape strategy
- Prepare internal presentations based on the progress of work on an on-going basis
- Prepare external poster and manuscript publications, when applicable, which is highly possible and encouraged.
- Support additional CPP team tasks as needed
Who You Are:
- Understanding of PK/PD principles is mandatory
- Population PK/PD Modeling skills are mandatory Proficiency in NONMEM, Monolix, or similar tools.
- Understanding of mixed-effects modeling and covariate analysis.
- Understand exposure-response modeling, survival analysis
- Basic programming and data handling skills are mandatoryR (especially packages like nlme, ggplot2, dplyr) or similar tools for data wrangling and visualization.
- Ability to digitalize literature data
- Ability to construct modeling analysis datasets
- Model-based or standard meta-analysis skills or experiences highly recommended, or demonstrated quick-to-mastery potential in this area
- Strong oral and written communication skills
To participate in the Biogen Internship or Co-op Program, students must meet the following eligibility criteria:
- Legal authorization to work in the U.S.
- At least 18 years of age prior to the scheduled start date.
- Currently enrolled in an accredited community college, college, university or skills program/apprenticeship.
Education Requirements
- PhD candidate or recent Post Doc is preferred
- Master degree or Pharm D with demonstrated modeling skills (see above) can be considered too
- Preferred majors/programs:Pharmaceutical Sciences;
- Clinical Pharmacology, Clinical Pharmacokinetics;
- Biostatistics or Applied Mathematics in life sciences;
- Biomedical Engineering
Job Level: Internship
Additional Information:
The base compensation range for this role is: $29.00-$33.00
The actual hourly wage offered will consider the candidate’s current academic level and degree candidacy, inclusive of Associate, Bachelor’s, Master’s, JD, MD, PhD and MBA programs. It will comply with state or local minimum wage requirements specific to the job location.
In addition to compensation, Biogen offers a range of benefits designed to support our educational employees, including, but not limited to:
- Company paid holidays
- Commuter benefits
- Employee Resource Groups participation
- 80 hours of sick time per calendar year
Why Biogen?
We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.
At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.
All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.
Total Views
0
Apply Clicks
0
Mock Applicants
0
Scraps
0
Similar Jobs

Sr. Clinical Compliance Specialist - FSP
Thermo Fisher · Remote, North Carolina, USA

Medical Specialist I-Dermatology-Roanoke, VA
Regeneron · Remote - Virginia

FSP Sr. Clinical Trial Coordinator
Thermo Fisher · Remote, California, USA

Medical Specialist I-Dermatology-Charleston-WV
Regeneron · Remote - West Virginia

Clinical Denial Lead
Cleveland Clinic · Remote Location
About Biogen

Biogen
PublicSpecializing in the treatment of neurological diseases.
5,001-10,000
Employees
Cambridge
Headquarters
Reviews
4.1
47 reviews
Work Life Balance
3.6
Compensation
4.7
Culture
4.1
Career
4.4
Management
3.8
84%
Recommend to a Friend
Pros
Opportunities for continuous learning and growth
Strong engineering culture with focus on code quality
Cutting-edge technology stack and interesting technical challenges
Cons
Organizational changes and restructuring can be disruptive
Fast-paced environment with tight deadlines
Work-life balance can be challenging during product launches
Salary Ranges
541 data points
Mid/L4
Senior/L5
Mid/L4 · SR Analyst, R&D Business Ops
1 reports
$131,388
total / year
Base
$114,250
Stock
-
Bonus
-
$131,388
$131,388
Interview Experience
47 interviews
Difficulty
3.5
/ 5
Duration
14-28 weeks
Offer Rate
36%
Experience
Positive 65%
Neutral 25%
Negative 10%
Interview Process
1
Phone Screen
2
Technical Interview
3
System Design
4
Behavioral
5
Team Fit
Common Questions
Tell me about a challenging project
System design question
Coding problem
Why this company
News & Buzz
FDA grants breakthrough therapy designation to Biogen’s litifilimab - Investing.com
Source: Investing.com
News
·
5w ago
Biogen’s Litifilimab Receives FDA Breakthrough Therapy Designation for Cutaneous Lupus Erythematosus, a Disease With No Targeted Treatment Options - Biogen
Source: Biogen
News
·
5w ago
FDA Accepts LEQEMBI® IQLIK™ (lecanemab-irmb) Supplemental Biologics License Application as a Subcutaneous Starting Dose for the Treatment of Early Alzheimer’s Disease under Priority Review - Biogen
Source: Biogen
News
·
5w ago
Biogen’s Alisha Alaimo On The Company’s Next Big Commercial Build - Citeline News & Insights
Source: Citeline News & Insights
News
·
6w ago