Research & Operations Tracks

Select a track aligned with your academic focus and career objectives. All tracks include mentorship, cross-functional collaboration, and a final project presentation to division leadership.

Biomedical Research

🧬 16 Weeks · Geneva / Boston

Conduct preclinical studies, assay development, and molecular profiling for novel therapeutic candidates.

In VitroCell BioData Analysis

Clinical Operations

📊 12 Weeks · Cambridge UK / Singapore

Support Phase I–III trial coordination, site monitoring, patient recruitment logistics, and compliance tracking.

GCPTrial ManagementSite Liaison

Pharmacovigilance & Safety

🛡️ 14 Weeks · Geneva / Remote

Analyze adverse event reports, support signal detection workflows, and contribute to risk management plans.

Argus/ArisGSignal DetectionRegulatory

Biotech & Gene Therapy

🧪 16 Weeks · Boston / Singapore

Work on CRISPR delivery systems, viral vector production, and next-gen gene editing pipelines.

CRISPRVector MfgGMP Labs

Regulatory Affairs

📜 12 Weeks · Cambridge UK / Geneva

Assist with CMC documentation, FDA/EMA submission packages, and cross-agency liaison strategies.

IND/NDACMCCompliance

Life Sciences Data Science

💻 14 Weeks · Hybrid / Remote

Build predictive models for drug discovery, optimize trial simulations, and deploy ML pipelines for omics data.

Python/RBioinformaticsML Ops

Eligibility & Requirements

We seek driven students and early-career researchers who demonstrate scientific rigor, ethical standards, and collaborative problem-solving.

  • Academic Status: Currently enrolled in an accredited undergraduate, master’s, or PhD program (must maintain enrollment for program duration)
  • Minimum GPA: 3.0/4.0 (or international equivalent)
  • Coursework: Completed foundational courses in biology, chemistry, bioinformatics, public health, or related disciplines
  • Laboratory Experience: Prior research, coursework labs, or clinical exposure preferred but not mandatory for all tracks
  • Language: Proficient in English (written & verbal); additional languages valued for regional sites
  • Authorization: Must be legally authorized to work in the host country; visa sponsorship available for select international candidates per local regulations

Application Timeline

Apply early. Cohort sizes are capped to ensure high-touch mentorship and lab capacity.

PhaseWindowDetailsStatus
Application OpensOct 15, 2025Portal access, track selection, document uploadOpen
Initial ReviewNov 1 – Dec 10Academic & experience screeningUpcoming
Technical AssessmentsDec 12 – Dec 28Case studies, lab simulations, or coding challenges (track-dependent)Upcoming
InterviewsJan 5 – Jan 31, 2026Virtual panels with scientists, ops leads, and HRUpcoming
Offers & OnboardingFeb 1 – Feb 28, 2026Contract signing, equipment provisioning, compliance trainingPending
Program StartMay 18, 2026Welcome week, site orientation, project kickoffsPending

Benefits & Perks

We invest in your growth, safety, and well-being throughout the internship period.

Competitive Stipend

Location-adjusted compensation plus housing/transportation allowance where applicable.

Dedicated Mentor

1:1 pairing with a senior scientist or operations lead for weekly guidance.

Lab & Tech Access

Full access to GMP facilities, high-performance computing clusters, and proprietary datasets.

Conversion Opportunities

78% of recent interns received full-time or PhD fellow offers within 12 months.

Conference Sponsorship

Funding to present your capstone project at regional or global industry symposiums.

Wellness & Safety

Comprehensive insurance, ergonomic workstations, mental health support, and rigorous biosafety protocols.

Frequently Asked Questions

Can I complete this internship remotely?

Lab-based tracks require on-site presence for safety and equipment access. Data Science, Pharmacovigilance, and Regulatory tracks offer approved hybrid or fully remote configurations depending on site capacity and compliance requirements.

Does Zenth Pharma provide academic credit?

Yes. We issue official letters of verification, detailed learning objectives, and mid/final evaluation reports tailored to your university’s requirements. Our HR team will coordinate directly with your academic advisor.

What happens to the IP I generate during the internship?

All inventions, datasets, and publications created during the internship are governed by our standard Intern IP Agreement. You will retain academic authorship rights for thesis work, subject to review for confidentiality and patent strategy alignment.

Is visa sponsorship available for international students?

Sponsorship is evaluated on a case-by-case basis and depends on local immigration policies. We actively support J-1, Tier 2, and equivalent research visas where legally permissible. Early application is strongly recommended.

How does the final project evaluation work?

Interns present their findings to a panel of division scientists, program managers, and leadership. Evaluations are based on scientific rigor, data interpretation, communication clarity, and practical applicability. Exceptional projects may fast-track to publication or internal pilot funding.

Begin Your Application

Prepare your CV, academic transcript, and a 1-page statement of research interests. Selected candidates will be contacted within 14 business days.