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Clinical Scientist

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Actalent

16d ago

  • Job
    Full-time
    Mid & Senior Level
  • Research & Development
  • Alameda

AI generated summary

  • You should have 3-5 years in clinical development within biotech or pharma and experience in clinical oncology studies involving molecular targeted or immunological therapies.
  • You will design study protocols, collaborate with clinical teams, develop documentation, analyze safety events, interpret data, and present findings in oncology while maintaining expertise in the field.

Requirements

  • Three to Five years of clinical development experience in the biotechnology or pharmaceutical industry
  • Participated in clinical oncology studies with molecular targeted or immunological therapies.

Responsibilities

  • 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.

FAQs

What is the primary focus of the Clinical Scientist role?

The primary focus of the Clinical Scientist role is to design, plan, and develop clinical evaluation research studies in oncology, specifically targeting solid tumors.

What type of experience is required for this position?

A candidate must have three to five years of clinical development experience in the biotechnology or pharmaceutical industry, with participation in clinical oncology studies involving molecular targeted or immunological therapies.

What are some responsibilities of the Clinical Scientist?

Responsibilities include collaborating with clinical teams to develop study protocols, conducting literature research, assisting with safety meetings, summarizing study results for documents and publications, and presenting scientific information to external customers.

Will I be required to prepare clinical development-related documents?

Yes, the Clinical Scientist will assist in authoring clinical development-related documents such as study synopses, protocols, and informed consent forms.

Is ongoing education and expertise in oncology required?

Yes, maintaining clinical and technical expertise in the therapeutic area of Oncology is essential for this role.

How will diversity, equity, and inclusion be approached in this position?

Diversity, equity, and inclusion are integral to the company culture, with efforts to hire diverse talent, maintain an inclusive environment, and provide growth opportunities for all employees.

Are there opportunities for professional development in this position?

Yes, the company is committed to ensuring growth opportunities for its employees, which may include training materials and presentations for various study-related venues.

What should I do if I need reasonable accommodations during the application process?

If you require reasonable accommodations due to a disability, you should email actalentaccommodation@actalentservices.com for assistance with the job application or interviewing process.

Will I collaborate with external experts in the field?

Yes, the Clinical Scientist will work with medical monitors to interact with clinical sites and thought leaders in oncology for efficient completion of clinical trials.

Is this position open to all qualified candidates?

Yes, the company is an equal opportunity employer and will consider all applications without regard to any characteristic protected by law.

Actalent

An Engineering and Sciences Services Company | People to Possible

Human Resources
Industry
5001-10,000
Employees

Mission & Purpose

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent’s global footprint and flexible delivery models ensure access to specialized talent where and when you need it. We promote consultant engagement through professional development and provide experiences to ensure continuous learning. Our people are the difference. Our expertise spans capabilities in engineering including product and manufacturing, systems and software, construction management, environmental, architecture and civil; and power and utilities. We focus on sciences capabilities in laboratory sciences, healthcare, and clinical research. Actalent is an operating company of Allegis Group, the global leader in talent solutions.