Clinical Scientist/Sr. Clinical Scientist

Corvus Pharmaceuticals; South San Francisco (CA); On-site; USD 130,000 - 150,000; Full time

Job summary

Corvus Pharmaceuticals is a clinical-stage biopharmaceutical company seeking a regulatory-minded clinician for hands-on support of clinical plans, protocols and regulatory documents. You will collaborate with the VP, Clinical Development and act as a Medical Monitor, coordinating data reviews and study conduct across sites.

Travel to field sites and meetings may be required. Ideal candidates hold a PhD/PharmD/RN/NP/PA and have 3+ years biotech experience in oncology, dermatology, or autoimmune

Qualifications

• PhD, PharmD, RN, NP or PA required.
• 3+ years biotech experience in oncology, dermatology or autoimmune disease.

Responsibilities

• Provides strategic input and development support for clinical plans and study protocols.
• Writes or assists in writing clinical plans, study protocols and amendments with VP, Clinical Development.
• Assists in writing Investigator Brochures, DSURs and other regulatory documents.
• Assists Medical Monitor responsibilities.
• Coordinates with Data Management to ensure timely data collection and data cleaning.
• Supports development of clinical operating guides and maintains secure study files.
• May travel to field sites and scientific meetings.
• Works on complex issues requiring in-depth evaluation of factors.
• Exercises judgment in selecting methods and evaluation criteria.

Skills

Teamwork

Communication

Microsoft Office

Education

PhD/PharmD/RN/NP/PA required

Tools

Microsoft Office

Job description

Corvus Pharmaceuticals is a clinical and late-stage biopharmaceutical company developing novel therapies with the potential to significantly improve the treatment of immune diseases and cancer. Our lead program, soquelitinib, is a first-in-class, oral therapy that selectively inhibits ITK to modulate and control parallel signaling pathways in the immune system. We are a small innovative and collaborative biotech company looking for like minded individuals to help grow the company and career. We work on-site alongside our colleagues to help build collaboration.

Role And Responsibilities

• Provides strategic input and development support for clinical plans and individual study protocols
• Writes or assists in writing of clinical plans and study protocols and protocol amendments in close collaboration with VP, Clinical Development
• Writes or assists in writing Investigator Brochures, DSURs and other regulatory documents Assist other team members in Clinical Development in the implementation and conduct of clinical trial which includes but not limited to review of enrollment packets, review of adverse events and all other clinical data generated during conduct of trial
• Assist in Medical Monitor responsibilities
• Work closely with Data Management to ensure that all relevant clinical data is collected in a timely manner and assist with cleaning of data listings
• Participates in the development of clinical operating guides and m_aintains secure study files Reviews results of these evaluations with appropriate management prior to implementation
• May require travel to field sites and scientific meetings
• Works on complex issues where analysis of situations or data requires an in-depth evaluation of variable factors
• Exercises judgment in selecting methods, techniques and evaluation criteria for obtaining results
• Determines methods and procedures on new assignments
• May coordinate activities of other personnel (team lead)

QUALIFICATIONS AND EDUCATION REQUIREMENTS

• PhD, PharmD, R.N, Nurse Practitioner or Physician Assistant required
• 3+ years of biotech experience (oncology, dermatology or autoimmune disease

PREFERRED SKILLS

• Excellent teamwork and collaboration skills
• Proficient with Microsoft Office
• Able to build effective working relationships throughout the organization internally and externally to achieve goals
• Flexibility and willingness to solve problems that fall outside of immediate area of expertise
• Clear and concise verbal and written communication skills and strong organizational skills, with an exceptional attention to detail
• Work independently in an interdisciplinary, fast-paced, often changing environment
• Committed to the values of integrity, accountability, transparency, and drive

Salary range - 130,000 - 150,000