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Full-time

Clinical Scientist, Clinical Development

$146K/yr – $161K/yr

Waltham, MAScience & PharmaceuticalPosted 22d ago

You'll complete your application on the employer's website.

Role overview

Job type

Full-time

Salary

$146K/yr – $161K/yr

Location

Waltham, MA

Posted

22 days ago

Job description

Responsibilities

Contributes to the development of clinical trial protocols, including patient selection criteria, study endpoints, and data collection methods

Monitors the data of clinical trials at study sites, ensuring adherence to protocols and good clinical practice (GCP) guidelines

Perform data review, reconciliation and standardization to ensure high quality outputs

Reviews clinical data to support in the assessment of the safety and efficacy of the investigational drug

Supports the development of clinical documents required during the clinical development process (including but not limited to: Clinical Study Protocols, Investigator Brochures, Clinical Study Reports)

Maintains knowledge of the therapeutic area, disease state, and potential drug effects

Assesses clinical data to help identify and analyze safety concerns and adverse events Stays current with relevant medical literature and clinical trial methodologies

Conducts literature reviews as needed for focused scientific questions or documentation

Works closely with other functions including clinical operations, regulatory affairs, medical affairs, biometrics, pre-clinical and project management teams to ensure data integrity during the clinical development process

Benefits

Equity

A performance-related bonus opportunity

Remote or hybrid work if commutable to the office in Waltham, MA, with in-office attendance required 3 days/week

A chance to be part of a vibrant startup culture where your work can directly impact bringing new medicines to patients

A supportive and inclusive team environment where everyone is encouraged to bring their authentic selves to work

Opportunities for professional growth and development

Oruka Therapeutics is advancing innovative biologics to redefine patient care standards in chronic skin diseases.

Waltham, Massachusetts, USA

https://www.orukatx.com/

Public Company

Total Funding

$1.16B

Key Investors

Viking Global Investors

2026-04-28

Post Ipo Equity· $700.35M

2025-09-17

Post Ipo Equity· $180M

2024-09-03

Post Ipo Equity· $275M

Leadership Team

Lawrence Klein

Chief Executive Officer

Recent News

The Motley Fool

These 2 Stocks Have Run Circles Around the Magnificent Seven This Year, and Wall Street Says There Is More Upside Ahead

2026-10-17

BioSpace

6 immunology targets to sustain a mammoth I&I market

2026-09-28

Qualifications

Advanced degree in life sciences, such as a PhD, PharmD or related field

Understanding of clinical trial methodologies and regulatory requirements

Experience in clinical study design, data analysis, data review and interpretation

Good written and verbal communication skills

Ability to work effectively in a collaborative, cross-functional environment

3 years experience

Required skills

Clinical Trial Methodologies, Regulatory Requirements, Clinical Study Design, Data Analysis, Clinical Data Review and Interpretation

Experience

3+ years

Interested in this role?

Apply directly on the employer's website — it only takes a few minutes.

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