Clinical Scientist

The Clinical Scientist will play a central role in the planning, execution, and reporting of one or more clinical studies, with a strong focus on oncology and solid tumors. This position involves extensive clinical data review, protocol development, and preparation of key clinical and regulatory documents. The role requires close collaboration with cross-functional study teams to ensure high-quality, compliant, and timely delivery of study milestones, with approximately 80% of the workload dedicated to detailed data review.

Responsibilities

• You will have key relationships internally withclinical project (study) team, and other study stakeholders.
• Review the scientific data and develop productknowledge to understand and communicate the relevant information for 1 or moreclinical studies.
• Develop and review various study protocols withminimal guidance including writing, reviewing, adjudication/resolution of crossfunctional comments, and ensuring a high-quality final document.
• Prepare and present the reports andpresentations on the various findings of the clinical research.
• Regularly review the information to check safetyprocedures, efficiency, and the lab data accuracy and correctness.
• Review and validate clinical study reports (CSRs) with a thorough understanding of the connection between the data and the CSR.
• Contribute to, coordinate, and review regulatorydocuments, Consent Forms (ICF), and other relevant study materials.
• Collaborate with all study team members including Clinical/Medical Affairs, Clinical Operations, Drug Safety,Regulatory Affairs and external vendors.
• Meet deadlines and milestones required basedupon assigned study goals.
• May be asked to participate in protocol design,writing and implementation to meet GCP, ICH and regulatory requirements.
• May be asked to provide input into the drug development and evidence generation process as a technical expert.

Must Have Qualifications

• Completion of a PharmD, PhD, MD, MS, PA, NP, or equivalent advanced degree in a relevant scientific or clinical discipline
• Minimum of 5 years of related clinical research or clinical development experience, including at least 5 years of data review responsibilities.
• At least 3 years of data review experience specifically in oncology, including experience with solid tumors.
• Demonstrated experience with TFL (tables, listings, figures) review and medical safety data review, including results evaluation and interpretation.
• Proficient knowledge and skills in program-specific data review, trend identification, and data interpretation.
• Strong proficiency in medical terminology and medical writing, particularly for clinical protocols, study documents, and clinical study reports.
• Proven ability to analyze clinical information succinctly and efficiently, with a strong focus on assessing data quality and presenting trial resul

Job Type & Location

This is a Contract position based out of Alameda, CA.

Pay and Benefits

The pay range for this position is $90.00 - $95.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully remote position.

Application Deadline

This position is anticipated to close on May 29, 2026.

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.

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.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.