Clinical Scientist

Job Title: Clinical Scientist Job Description As a Clinical Scientist, you will play a pivotal role in fostering key relationships internally with clinical project teams and other study stakeholders. You will be responsible for reviewing scientific data and developing product knowledge, enabling you to communicate relevant information for one or more clinical studies. Additionally, you will develop and review various study protocols with minimal guidance, ensuring high-quality final documents. You will prepare and present reports and presentations on clinical research findings, regularly reviewing information to verify safety procedures, efficiency, and data accuracy. Responsibilities Review scientific data and develop product knowledge to communicate relevant information for clinical studies. Develop and review study protocols, ensuring high-quality final documents. Prepare and present reports and presentations on clinical research findings. Regularly review information to verify safety procedures, efficiency, and data accuracy. Review and validate clinical study reports (CSRs) with a thorough understanding of the data connection. Contribute to, coordinate, and review regulatory documents, Consent Forms (ICF), and other study materials. Collaborate with study team members including Clinical/Medical Affairs, Clinical Operations, Drug Safety, Regulatory Affairs, and external vendors. Meet deadlines and milestones based on assigned study goals. Participate in protocol design, writing, and implementation to meet GCP, ICH, and regulatory requirements. Provide input into the drug development and evidence generation process as a technical expert. Conduct data review, which comprises 80% of the role. Essential Skills 5 years of data review experience, with 3+ years in oncology. Experience with TFL Review, Medical Safety Data Review, and Results evaluation/review. Master's degree or higher in a related field. Proficient knowledge and skills to support program-specific data review, trend identification, and data interpretation. Proficient in Medical Terminology and medical writing skills. Knowledge of ICH, GCP, and other regulatory guidelines. Ability to analyze clinical information efficiently with strong written communication skills. Strong communication, presentation, analytic, and strategic capabilities. Ability to collaborate effectively with medical experts and cross-functional teams. Additional Skills & Qualifications Completion of PharmD, PhD, MD, MS, PA, NP, or equivalent education and experience. Experience in oncology and solid tumors is required. Work Environment This role is entirely remote, with no travel required. 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 Aug 21, 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. 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 [email protected] 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.