Open for applications

Internship opportunity for Clinical Pharmacology/Clinical Science Student Sherwood Pharmaceuticals

About the vacancy

R&D
Rare & Orphan Diseases
Internship Master’s Degree (WO) Internship Full time 600 Leiden, South Holland, Netherlands

About Your Next Job

Sherwood Pharmaceuticals is a young startup exploring the first-ever treatment for Cri du Chat syndrome, a rare genetic disease. At Sherwood Pharmaceuticals we are assessing a drug repurposing opportunity for the potential treatment of Cri du Chat syndrome (CdCS) (a.k.a. 5p Monosomy). This rare disease affects 1:20,000 births but currently there are no dedicated treatments available. Get involved with an ambitious company working closely alongside an experienced founder team, knowledgeable patent attorneys and ongoing collaboration with academic partners and patient advocacy foundations.

This clinical pharmacology internship is an exciting opportunity for someone motivated to drive therapies into the hands of patients and their families as quickly as possible. Working closely with the CEO and Chief Development Officer to gain perspectives on the process of drug development – from bench to bedside. You will report to the Chief Development Officer.

The duration of the internship is 9 months.

What you will do:

  • Learn to inventorize relevant data/reports available and thus assist in establishing selection criteria for short-listing of compounds most suitable to CdCS patients.
  • Systematically evaluate shortlisted compounds e.g., based on clinical study reports (including pharmacokinetics and outcome measures) for adults and pediatrics
  • Conduct initial formulation feasibility review based on literature, and interview experts in the field
  • Deliverables: a comparison report for compound prioritization
  • Work closely with the academic collaboration partner
  • Attend relevant events and conferences, and be a full member of the team!

Your profile:

  • Master’s degree student in clinical pharmacology/clinical sciences
  • Affinity for neurosciences
  • Comfortable working in a hybrid environment and in an international setting
  • Self-driven, organized and enthusiastic

The offer:

  • Full-time for 9 months, starting 1 October 2026
  • Monthly student stipend of  EUR 600
  • Opportunity to make an impact on the quality of life for Cri du Chat patients and their families

About Your Next Colleagues

Get involved with an ambitious company working closely alongside an experienced founder team, knowledgeable patent attorneys and ongoing collaboration with academic partners and patient advocacy foundations.


About Your Tasks and Responsibilities

The duration of the internship is 9 months.

What you will do:

  • Learn to inventorize relevant data/reports available and thus assist in establishing selection criteria for short-listing of compounds most suitable to CdCS patients.
  • Systematically evaluate shortlisted compounds e.g., based on clinical study reports (including pharmacokinetics and outcome measures) for adults and pediatrics
  • Conduct initial formulation feasibility review based on literature, and interview experts in the field
  • Deliverables: a comparison report for compound prioritization
  • Work closely with the academic collaboration partner
  • Attend relevant events and conferences, and be a full member of the team!

About Your Skills and Experience

Your profile:

  • Master’s degree student in clinical pharmacology/clinical sciences
  • Affinity for neurosciences
  • Comfortable working in a hybrid environment and in an international setting
  • Self-driven, organized and enthusiastic

About Your Benefits

  • Hybrid setting
  • International team
  • Learn from expert



Only apply if...

Only for serious applicants.


You are eligible to work in EU

We only accept applicants who are eligible to work in the EU


Contact person

Irisa Ono

logo of Sherwood Pharmaceuticals

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Sherwood Pharmaceuticals is a young startup exploring the first-ever treatment for Cri du Chat syndrome, a rare genetic disease. At Sherwood Pharmaceuticals we are assessing a drug repurposing opportunity for the potential treatment of Cri du Chat syndrome (CdCS) (a.k.a. 5p Monosomy). This rare disease affects 1:20,000 births but currently there are no dedicated treatments available. Get involved with an ambitious company working closely alongside an experienced founder team, knowledgeable patent attorneys and ongoing collaboration with academic partners and patient advocacy foundations.



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