Logo of Huzzle

Clinical Scientist

image

Actalent

13d ago

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

AI generated summary

  • You need 3-5 years of clinical development experience in biotech or pharma and participation in oncology studies involving molecular targeted or immunological therapies.
  • You will design clinical studies in oncology, collaborate with teams on protocols, analyze data, prepare documents, and deliver presentations while maintaining expertise in solid tumors.

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

  • In collaboration with clinical and project teams of the company, the Clinical Scientist designs, plans and develops clinical evaluation research studies in oncology with focus on solid tumors. This position may assist in or prepare and author clinical development related documents including study synopses and protocols. Summarizes study results for preparation of documents and publications. Supports project teams with scientific information and provides progress updates related to the assigned clinical studies. Must have experience with clinical studies in oncology.
  • 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 position?

The primary focus of the Clinical Scientist position is on designing, planning, and developing clinical evaluation research studies in oncology, particularly with a focus on solid tumors.

What qualifications are required for this position?

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

What are the key responsibilities of the Clinical Scientist?

Key responsibilities include designing study protocols, collaborating with clinical teams, conducting literature research, developing necessary documentation, participating in safety meetings, and supporting the preparation of regulatory reports and publications.

What is the role of the Clinical Scientist in relation to clinical sites and thought leaders?

The Clinical Scientist will work with the medical monitor to facilitate interactions with clinical sites and thought leaders in oncology to ensure efficient completion of clinical trials.

What types of documents will the Clinical Scientist be involved in preparing?

The Clinical Scientist may assist in preparing clinical development documents such as study synopses, protocols, Informed Consent Forms, Case Report Forms, and publications.

Is experience in oncology required for this role?

Yes, experience with clinical studies in oncology is required for this position.

How does Actalent approach diversity, equity, and inclusion?

Actalent approaches diversity, equity, and inclusion by hiring diverse talent, maintaining an inclusive environment, building a culture of care and recognition, and ensuring growth opportunities for all employees.

What can be expected regarding the collaboration with internal study team members?

The Clinical Scientist will collaborate with clinical operations and other internal study team members throughout the development of clinical study materials and documentation.

What opportunities does Actalent provide for learning and professional development?

Actalent ensures growth opportunities for its employees, fostering a culture of engagement, recognition, and continuous improvement.

How can candidates request accommodations during the application process?

Candidates may request reasonable accommodations for the job application or interview process due to a disability by emailing actalentaccommodation@actalentservices.com for alternative options.

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.