Oncology Clinical Development Expertise for Pharma and Biotech

Flexible Oncology Support

Oncostrata provides experienced oncology physicians and clinical scientists to support pharmaceutical and biotechnology clinical development programmes from early development through Phase III and regulatory submission.

Our specialists work alongside clinical development teams, providing expertise across trial design and execution, medical and scientific oversight, data review, safety, efficacy and delivery.

Services

Embedded Scientific Expertise

Oncostrata physicians and scientists integrate into cross-functional teams to provide scientific input into all aspects of late-stage clinical development programmes.

Oncology clinical development is becoming increasingly specialised. Finding the right individual is no longer simply about experience - it is about matching scientific expertise, tumour knowledge and clinical development capability to the specific needs of each programme.

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Let’s work together.

Whatever the scientific challenges facing your trial, we can help.

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How We Work

The right expertise for the right programme

Every oncology programme is different.

Success depends on finding professionals with the right combination of clinical development experience, therapeutic expertise and scientific understanding.

We help identify experienced:

Oncology Medical Monitors
Clinical Scientists
Clinical Development Scientists
Physician Scientists
Medical Directors
Translational and Biomarker Scientists

Carefully matched to each programme's:

Tumour indication
Therapeutic modality (ADCs, immuno-oncology, cell therapy, cancer vaccines, radiopharmaceuticals, targeted therapies)
Molecular pathway and mechanism of action
Phase of development
Scientific and operational complexity