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 with clinical project (study) team, and other study stakeholders.

* Review the scientific data and develop product knowledge to understand and communicate the relevant information for 1 or mo reclinical studies.

* Develop and review various study protocols with minimal guidance including writing, reviewing, adjudication/resolution of cross functional comments, and ensuring a high-quality final document.

* Prepare and present the reports and presentations on the various findings of the clinical research.

* Regularly review the information to check safety procedures, 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 regulatory documents, 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 Pharm

D, 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.

Final date to receive applications

This position is anticipated to close on Jun 12, 2026.

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