Seeking 1 Clinical Scientist

Hybrid role, onsite in Alameda, CA

Description:

• In collaboration with the clinical teams for a specific product candidate, designs, prepares and initiates study protocols and other required documentation in compliance with project plans, federal regulations, GCP and good medical practice.

• Conducts appropriate literature research for the assigned clinical product candidate.

• Works with medical monitor to enable interaction with clinical sites and thought leaders in oncology to assist sites in efficient completion of clinical trials

• Collaborates with clinical operations and other internal study team members to develop Informed Consent Forms, Case Report Forms, and CRF instructions.

• Collaborates with clinical operations and other team members in the development of agendas, training materials, and presentation for site visits, investigator meetings, and other study related venues

• Participates in internal safety meetings, analyzes, and reports potential safety events in coordination with medical monitor.

• Collaborates with team members in clinical review and interpretation of study data in support for preparation of reports for health authorities including regulatory filing documentation and study close-out reports.

• Helps to write and/or review product specific abstracts, publications, and supports the development of presentations for scientific meetings.

• Proactively provides feedback on emerging clinical and competitive trends.

• Delivers high quality scientific presentations on investigational agents to physicians and other key external customers.

• Maintains clinical and technical expertise in the therapeutic area of Oncology.

Skills:

Clinical development, Oncology, clinical review, clinical science, study protocols, consent forms

Additional Skills & Qualifications:

• Pharm.D., PhD, or M.D. or equivalent education and a minimum of five years of related experience.

• Equivalent combination of education and experience.

Three to Five years of clinical development experience in the biotechnology or pharmaceutical industry or a combination of academia and industry.

• Participated in clinical oncology studies with molecular targeted or immunological therapies.

Experience Level:

Intermediate Level

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

• Hiring diverse talent
• Maintaining an inclusive environment through persistent self-reflection
• Building a culture of care, engagement, and recognition with clear outcomes
• Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.