Clinical Scientist III

TechDigital Group; West Sacramento (CA); On-site; USD 80,000 - 110,000; Full time

Job summary

An innovative firm is seeking a Senior Clinical Affairs Scientist to support clinical trials in microbiology. This role involves writing clinical plans, selecting organisms for testing, and analyzing data. The ideal candidate will possess a strong educational background in life sciences, with significant experience in clinical settings. You will collaborate with cross-functional teams, ensuring adherence to good clinical practices and maintaining meticulous documentation. Join a dynamic environment where your skills will contribute to groundbreaking research and development in the field of microbiology. If you thrive in a fast-paced, evolving landscape, this opportunity is perfect for you.

Qualifications

• 5+ years experience with a Bachelor's or 3+ years with a Master's in Life Science.
• Strong communication and problem-solving skills are essential.

Responsibilities

• Write clinical plans, protocols, and reports for microbiology trials.
• Interpret and analyze clinical trial data, conducting data reviews.

Skills

Communication Skills

Problem Solving

Attention to Detail

Organizational Skills

Education

Bachelor's degree in Life Science

Master's degree in Life Science

Tools

Excel

Word

Job description

Job Description – Clinical Scientist III

Location: West Sacramento, CA (HYBRID)

The Senior Clinical Affairs Scientist will support the Clinical Affairs team during Microbiology antimicrobial susceptibility testing (AST) clinical trials. Working under a Clinical project lead, the incumbent will:

1. Write clinical plans, protocols, and reports for Microbiology clinical trials.
2. Select organisms for clinical trial testing.
3. Interpret and analyze clinical trial data, conducting data reviews.
4. Update project lead(s) with data and any issues.
5. Work in cross-functional teams.

Position Requirements:

1. Bachelor's degree in a Life Science or related field with 5+ years experience OR Master's degree in Life Science or related field with 3+ years of experience.
2. Strong communication skills with the ability to work in a multidisciplinary team environment.
3. Ability to problem solve is a must.
4. Knowledge of good clinical practices (GCP), good documentation practices (GDP), and strong writing skills desired.
5. Attention to detail and good organizational skills required.
6. Ability to be flexible and work in a rapidly changing task environment and with a variety of tasks.
7. Familiarity with Excel, Word, and data analysis is desired.