Clinical Scientist, Clinical Development

Oruka Therapeutics; Waltham (MA); Hybrid; USD 140,000 - 155,000; Full time

Job summary

Oruka Therapeutics, a leader in developing novel biologics for chronic skin diseases, seeks a Clinical Scientist in Waltham, MA (Hybrid). This role includes the operation of clinical trials, ensuring data quality, and close collaboration with cross-functional teams. The ideal candidate will hold an advanced life sciences degree and have three years of relevant experience.

Benefits

Competitive salary and benefits package

Opportunities for professional growth and development

Qualifications

• Advanced degree in life sciences required.
• 3 years experience in clinical trial methodologies and regulatory requirements.
• Good written and verbal communication skills are essential.

Responsibilities

• Contributes to clinical trial protocol development, patient selection criteria, and study endpoints.
• Monitors clinical trial data at study sites to ensure adherence to protocols.
• Supports the generation of clinical documents required during the development process.

Skills

Communication

Data Analysis

Scientific Knowledge

Collaboration

Education

PhD in life sciences

PharmD

Job description

About Us:

Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. We have raised nearly $500M since inception in February 2024 from top-tier investors and our first program is expected to be in the clinic in the first quarter of 2025. For more information, visit www.orukatx.com

As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture.

Job Title: Clinical Scientist, Clinical Development

Location: Hybrid – Waltham, MA. Candidates will be required to be in-office in 3 days/week. Remote considered.

Role Overview:

The Clinical Scientist plays a key role in the execution and operational support of clinical trials, assisting in the collection and review of clinical data to ensure study success. This role involves supporting protocol development, study implementation, data review, and documentation preparation to align with clinical development goals. The Clinical Scientist collaborates closely with cross-functional teams to ensure the generation of high-quality clinical data. Additionally, they work closely with the Medical Director, Clinical Development to execute key tasks.

Key Responsibilities:

• Clinical Trial Design and Oversight:
• 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).
• Scientific Expertise:
• 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.
• Cross-Functional Collaboration:
• 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.
  

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
  
  

Compensation:

• An appropriate financial package will be developed for the successful candidate to include a competitive base salary and equity, with a performance-related bonus opportunity.
• The anticipated salary range for candidates, who will work in Waltham, MA (remote may be considered) is $140,000 to $155,000. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Oruka is a multi-state employer and this salary range may not reflect positions that work in other states.
  
  

We're looking forward to hearing how you can contribute to our team and mission. Join us in shaping the future of our company and making a real impact every day.

Salary Range for the Role

$140,000—$155,000 USD

What We Offer:

• A chance to be part of a vibrant small-company culture where your work can directly impact bringing new medicines to patients.
• Competitive salary and benefits package.
• Opportunities for professional growth and development.