Clinical Research Scientist

Top Quality Recruitment (TQR); Hot Springs (AR); On-site; USD 70,000 - 120,000; Full time

Job summary

Top Quality Recruitment (TQR) is seeking a Clinical Research Scientist in the United States, Arkansas region, to support clinical trials, regulatory processes, and research programs within the life sciences sector.

The role emphasizes coordinating and executing research projects, preparing trial protocols, and ensuring regulatory compliance across internal and external stakeholders while contributing to technical documentation and data-driven recommendations for product development.

Qualifications

• Experience with grant writing.
• Experience developing or submitting clinical trial protocols.
• Regulatory affairs experience within life sciences, pharmaceutical, biotechnology, or medical device industries.
• Clinical trial project management experience.
• Advanced degree (MS, MPH, PharmD, or PhD).

Responsibilities

• Support the planning, coordination, and execution of clinical research projects and trials.
• Assist with the development and submission of clinical trial protocols and related documentation.
• Collaborate with internal and external stakeholders to ensure regulatory compliance.
• Contribute to scientific and technical documentation, including grant proposals and study reports.
• Manage timelines, deliverables, and cross-functional communication for research initiatives.
• Analyze scientific data and provide recommendations to support product development and clinical programs.
• Stay current on regulatory trends, industry standards, and best practices in life sciences.

Skills

Grant writing

Clinical trial protocols

Regulatory affairs

Clinical project management

Advanced degree in life sciences

Education

Bachelor's, Master's, or PhD in Microbiology, Life Sciences, Biology, Biomedical Sciences

Infectious Disease experience

Surgical products or procedures experience

Job description

The Clinical Research Scientist will bring a strong scientific background and experience supporting clinical trials, regulatory processes, and research programs within the life sciences industry.

Key Activities

• Support the planning, coordination, and execution of clinical research projects and trials.
• Assist with the development and submission of clinical trial protocols and related documentation.
• Collaborate with internal and external stakeholders to ensure compliance with regulatory requirements.
• Contribute to scientific and technical documentation, including grant proposals, study reports, and regulatory submissions.
• Manage timelines, project deliverables, and cross-functional communication for research initiatives.
• Analyze scientific data and provide recommendations to support product development and clinical programs.
• Stay current on regulatory trends, industry standards, and best practices within the life sciences field.

Preferred Skills

• Experience with grant writing.
• Experience developing or submitting clinical trial protocols.
• Regulatory affairs experience within the life sciences, pharmaceutical, biotechnology, or medical device industries.
• Clinical trial project management experience.
• Advanced degree (MS, MPH, PharmD, or PhD).

Educations & Experience

• Bachelor's, Master's, or PhD in Microbiology, Life Sciences, Biology, Biomedical Sciences, or a related field.
• Experience in one or more of the following areas:
• Infectious Disease.
• Surgical Products or Procedures.
• Strong scientific, analytical, and computer skills.

TQR is an equal-opportunity employer that encourages diversity. We will consider all applications.

Accommodation for applicants with disabilities is available upon request.