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Job Title: Clinical ScientistJob Description

Collaborate with clinical teams for a specific product candidate, designing, preparing, and initiating study protocols and other required documentation in compliance with project plans, federal regulations, GCP, and good medical practice. Conduct appropriate literature research for the assigned clinical product candidate. Work with the medical monitor to enable interaction with clinical sites and thought leaders in oncology to assist sites in the efficient completion of clinical trials. Collaborate with clinical operations and other internal study team members to develop Informed Consent Forms, Case Report Forms, and CRF instructions. Develop agendas, training materials, and presentations for site visits, investigator meetings, and other study-related venues. Participate in internal safety meetings, analyze, and report potential safety events in coordination with the medical monitor. Collaborate in the clinical review and interpretation of study data to support the preparation of reports for health authorities, including regulatory filing documentation and study close-out reports. Write and/or review product-specific abstracts, publications, and support the development of presentations for scientific meetings. Proactively provide feedback on emerging clinical and competitive trends. Deliver high-quality scientific presentations on investigational agents to physicians and other key external customers. Maintain clinical and technical expertise in the therapeutic area of Oncology.

Hard Skills

• Clinical trial implementation

• Drug development process

• Clinical Science

• Study protocols

• Consent forms

• Global phase 1/2 trial experience

• QC data review for late development

Soft Skills

• Strong analytical skills

• Business communication skills

• Highly organized

• Good public speaking and presentation skills

• Creativity

• Collaboration

• Comfortability with cross-functional exposure

Job Type

This is a contract position with a duration of 12 Month(s).

Work Site

This is a fully remote position.

Work Environment

Remote, 10-25% travel requirement for group meetings

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 (%20actalentaccommodation@actalentservices.com) for other accommodation options.