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Clinical Scientist

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Actalent

3mo ago

  • Job
    Full-time
    Junior, Mid & Senior Level
  • Research & Development
    Healthcare
  • Alameda
    Remote

AI generated summary

  • You must have experience in clinical trial implementation, drug development, QC data review, and study protocols, along with strong analytical, communication, and collaboration skills.
  • You will design study protocols, collaborate with teams, conduct literature research, support data analysis, develop training materials, and present findings in oncology.

Requirements

  • Clinical trial implementation
  • Drug development process
  • Clinical Science
  • Study protocols
  • Consent forms
  • Global phase 1/2 trial experience
  • QC data review for late development
  • Strong analytical skills
  • Business communication skills
  • Highly organized
  • Good public speaking and presentation skills
  • Creativity
  • Collaboration
  • Comfortability with cross-functional exposure

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 job title for this position?

The job title for this position is Clinical Scientist.

Is this position remote or in-person?

This is a fully remote position.

What is the duration of the contract for this position?

The duration of the contract for this position is 12 months.

What are the primary responsibilities of a Clinical Scientist in this role?

The primary responsibilities include collaborating with clinical teams, designing study protocols, conducting literature research, developing consent forms and case report forms, analyzing safety events, and preparing reports for health authorities.

What type of experience is required for this position?

Global phase 1/2 trial experience and knowledge of the drug development process are required for this position.

What hard skills are necessary for this role?

Necessary hard skills include clinical trial implementation, clinical science, study protocols, consent forms, and QC data review for late development.

Are there specific soft skills that are important for a Clinical Scientist?

Yes, important soft skills include strong analytical skills, business communication skills, organizational skills, public speaking, creativity, collaboration, and comfortability with cross-functional exposure.

Is there any travel required for this position?

Yes, there is a travel requirement of 10-25% for group meetings.

What kind of company culture does Actalent promote?

Actalent promotes a culture of diversity, equity, and inclusion, focusing on hiring diverse talent and maintaining an inclusive environment.

How can applicants request reasonable accommodations during the application process?

Applicants can request reasonable accommodations by emailing actalentaccommodation@actalentservices.com for options.

Is Actalent an equal opportunity employer?

Yes, Actalent is an equal opportunity employer and considers all applications without regard to characteristics protected by law.

What role does the Clinical Scientist play in safety meetings?

The Clinical Scientist participates in internal safety meetings, analyzes potential safety events, and works in coordination with the medical monitor to report findings.

Are there opportunities for growth within the company?

Yes, Actalent ensures growth opportunities for its employees.

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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.