Clinical Research Scientist

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

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.

Benefits

Referral bonus

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

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

Title: Clinical Research Scientist Duration: 12 Months (Possibility of Extension) Location Woodcliff lake NJ

Job Responsibilities:

• The incumbent is responsible for, but not limited to the following:
• Assist in the planning, implementation, managing, and reporting of Phase I-III clinical studies
• Prepare and review project and study documents including clinical trial protocols, clinical study reports, patient SAE narratives, clinical sections of registration dossier documents (ISS, ISE, Investigator Brochure, etc)
• Performs literature search and data analysis to address research questions
• In collaboration with other clinical staff and/or an external CRO, monitoring clinical trial conduct (enrollment, GCP practices, handling of safety issues, etc.)
• Assisting in database cleaning, review of study results, and interpretation of results
• Adhering to key performance indicators for clinical study development, conduct, and reporting
• Individual contributor with specialized knowledge
• Presents concepts, facts, and reports and advises on key trends and issues
• Troubleshooting routine site inquiries
• Work is completed under limited supervision
• Supports the planning, execution and reporting of clinical programs/trials
• Contributes to risk resolution by escalating and monitoring project risks

Qualifications

Qualifications

• Minimum of 2-5 years of experience in clinical research in the pharmaceutical industry
• A thorough understanding of clinical research methodology including study design, protocol writing, and CRF preparation is required, as is a knowledge of GCP and local regulatory requirements
• Working knowledge of the IND/NDA/CTD/MAA process acquired through direct industrial experience preferred
• Knowledge of medical, scientific and clinical research techniques in the oncology therapeutic area;
• Bachelor’s Required. Doctoral (PharmD or PhD) or MD degree preferred .

Additional Information

Feel free to forward my email to your friends/colleagues who might be available. We do offer referral bonus

Thank you for your time and consideration. I look forward to hearing from you!

Kind Regards

Clinical Recruiter

Integrated Resources , Inc.

(DIRECT BOARD) # 732-844-8716 (F) 732-549-5549

LinkedIn: https://www.linkedin.com/in/ruchi-kumari

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