Key Responsibilities:

Coordinate and manage oncology clinical trials from initiation to completion.Recruit, screen, and enroll study participants.Obtain informed consent and ensure ethical conduct of clinical trials.Collect, process, and manage clinical data and samples.Monitor patient safety and report adverse events.Maintain accurate and up-to-date study documentation.Liaise with investigators, sponsors, and regulatory authorities.Ensure compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements.Assist in the preparation of study protocols, reports, and publications.

Qualifications:

Bachelor's degree in a related field (e.g., Nursing, Life Sciences, Public Health).Minimum of 2 years of experience in clinical research, preferably in oncology.Knowledge of clinical trial processes, regulations, and GCP guidelines.Strong organizational and time-management skills.Excellent communication and interpersonal skills.Proficiency in electronic data capture systems and Microsoft Office Suite.Ability to work independently and as part of a multidisciplinary team.Certification as a Clinical Research Coordinator (CCRC) or Clinical Research Professional (CCRP) is a plus.

Pay and Benefits

The pay range for this position is $30.00 - $40.00

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 onsite position in Sacramento,CA.

Application Deadline

This position will be accepting applications until Jan 1, 2025.

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.