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1–2 jobs· newest first

Part Time Research Support - Radiation OncologyNew
psu.wd1.myworkdayjobs.com/PSU_Staff · Hershey, US
$16–$16Part-time
Director, Regulatory Affairs, BeNeLux
Revolution Medicines · Amsterdam, Netherlands
Hybrid · Senior

+10K new in the last hour

Part Time Research Support - Radiation Oncology

psu.wd1.myworkdayjobs.com/PSU_Staff · Posted Nov 10, 2026

Hershey, Pennsylvania, United States
Part-time
$16–$16 per hour

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Provide intermediate-level support for biomedical and translational research projects focused on radiation response in head and neck cancer.

Compensation

paying $16 per hour

Responsibilities

Assist with ongoing laboratory research projects under the supervision of the principal investigator and other research personnel.
Perform routine mammalian cell culture procedures, including cell counting, cell passaging, cryopreservation, and preparation of cells for experiments.
Assist with laboratory experiments evaluating cancer cell responses to radiation and potential therapeutic treatments.
Perform molecular and cellular biology techniques, including preparation of samples and reagents and assistance with protein analysis and cell-based assays.
Conduct/assist in laboratory experiments involving radiation treatment, cell viability, clonogenic survival, and other assays to evaluate cellular responses to radiation and potential therapeutic interventions.

Requirements

Bachelor's degree in a relevant life sciences discipline

Skills

mammalian cell culture aseptic laboratory techniques experimental data collection basic statistical analysis scientific data presentation molecular and cellular biology techniques

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Director, Regulatory Affairs, BeNeLux

Revolution Medicines · Posted Nov 5, 2026

Amsterdam, North Holland, Netherlands
Hybrid
Senior
10+ years

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Lead regulatory strategy and execution for Belgium, Netherlands and Luxemburg, ensuring compliance and launch readiness for the company’s first oncology product.

Responsibilities

Develop and execute regulatory strategy for BeNeLux
Ensure first product launch readiness and compliance
Coordinate cross-functional regulatory activities
Implement global and regional governance model
Provide regulatory support for assigned products

Requirements

Master’s / PhD degree in scientific or medical discipline
Nice to have: Oncology experience
Nice to have: Biotech start-up/scale-up experience
Nice to have: Early and late-stage clinical assets experience

Skills

European Regulatory Affairs EU market approvals Regulatory submissions Product lifecycle management Knowledge of EU regulatory framework Dutch, English, French language skills

Scientific data presentation

Networking with regulatory bodies

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