Clinical Research Scientist - Phase I-III Trials

Integrated Resources Inc.; Woodcliff Lake (NJ); On-site; USD 80,000 - 110,000; Full time

Benefits offered by this job

Referral bonus

Job summary

A leading staffing firm seeks a Clinical Research Scientist for a 12-month engagement in Woodcliff Lake, NJ. The role involves managing clinical studies and analyzing data while adhering to regulatory requirements. Ideal candidates have 2-5 years in clinical research, a solid understanding of study design, and a relevant degree. This position offers an opportunity to contribute to impactful clinical programs.

Qualifications

• 2-5 years of experience in clinical research in the pharmaceutical industry.
• Thorough understanding of clinical research methodology including study design and protocol writing.
• Knowledge of GCP and local regulatory requirements.

Responsibilities

• Assist in planning, implementation, and reporting of Phase I-III clinical studies.
• Prepare project documents including clinical trial protocols and reports.
• Monitor clinical trial conduct, ensuring adherence to guidelines.

Skills

Clinical research methodology

Study design

Protocol writing

Data analysis

Regulatory requirements

Education

Bachelor’s degree

PharmD or PhD degree preferred

Job description

A leading staffing firm seeks a Clinical Research Scientist for a 12-month engagement in Woodcliff Lake, NJ. The role involves managing clinical studies and analyzing data while adhering to regulatory requirements. Ideal candidates have 2-5 years in clinical research, a solid understanding of study design, and a relevant degree. This position offers an opportunity to contribute to impactful clinical programs.