
Clinical Research Scientist
Welcome to Eli Lilly and Company, where we are dedicated to improving the lives of patients through innovative and life-saving therapies. As a Clinical Research Scientist, you will play a crucial role in advancing our research and development efforts. We are seeking a highly motivated and detail-oriented individual with a passion for scientific discovery and a strong understanding of clinical trial design and execution. Join our dynamic team and be a part of making a difference in the lives of millions of people worldwide.
- Design and oversee clinical trials in accordance with regulatory guidelines and company protocols.
- Develop and maintain study-related documents, including protocols, informed consent forms, and study reports.
- Collaborate with cross-functional teams to ensure efficient and timely execution of clinical trials.
- Monitor trial progress and identify and troubleshoot issues that may impact study timelines or data integrity.
- Analyze and interpret clinical data to support drug development decisions and regulatory submissions.
- Conduct literature reviews and stay up-to-date with scientific advancements in relevant therapeutic areas.
- Communicate study updates and results to internal and external stakeholders, including investigators and regulatory authorities.
- Ensure compliance with all applicable regulations and guidelines, including Good Clinical Practice (GCP) and International Council on Harmonization (ICH) guidelines.
- Participate in the development of clinical development plans and study protocols.
- Contribute to the preparation of regulatory submissions, including Investigational New Drug (IND) applications and New Drug Applications (NDA).
- Mentor and train junior team members on clinical research processes and guidelines.
- Participate in departmental and cross-functional meetings to provide updates on trial progress and discuss potential issues or challenges.
- Collaborate with external vendors, such as Contract Research Organizations (CROs), to ensure high-quality and timely execution of clinical trials.
- Contribute to the development and implementation of new processes and procedures to improve efficiency and quality in clinical research.
- Maintain accurate and complete records and documentation in accordance with company and regulatory requirements.
Minimum Of 3-5 Years Of Experience In Clinical Research, Preferably In The Pharmaceutical Industry.
Advanced Degree In A Relevant Scientific Field, Such As Pharmacology, Biochemistry, Or Molecular Biology.
Strong Knowledge Of Fda Regulations And Guidelines Related To Clinical Trials And Drug Development.
Experience In Designing And Implementing Clinical Study Protocols, Analyzing And Interpreting Data, And Writing Clinical Study Reports.
Excellent Communication And Interpersonal Skills, As Well As The Ability To Work Independently And In A Team Setting.
Project Management
Data Analysis
statistical analysis
Quality Control
Drug development
Scientific writing
Regulatory compliance
Literature Review
Protocol Development
Clinical Trial Design
Pharmacovigilance
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Time management
creativity
Critical thinking
Teamwork
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Clinical Research Scientist in Austin, TX, USA is between $73,000 and $144,000 per year. This range can vary based on factors such as level of experience, education, and the specific company or organization hiring for the position. Salaries may also be influenced by the type and complexity of research being conducted, as well as the demand for clinical research scientists in the Austin area.
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Eli Lilly and Company is an American pharmaceutical company headquartered in Indianapolis, Indiana, with offices in 18 countries. Its products are sold in approximately 125 countries. The company was founded in 1876 by, and named after, Col. Eli Lilly, a pharmaceutical chemist and veteran of the American Civil War.

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