Jr. Clinical Trials Data Specialist

As a Jr. Clinical Trials Data Specialist at Tempus, you will work closely with cross-functional teams to develop customized clinical reports, analyze patient records and testing results, and identify potential clinical trials. You'll also be responsible for ensuring quality control in the report workflow and supporting various projects within the team.

Candidates for the Jr. Clinical Trials Data Specialist role at Tempus must possess at least a BS degree in Genetics, Molecular Genetics, Cancer Biology, or Biological Sciences. Additionally, strong communication skills, flexibility, and a quick willingness to learn new skills are essential for success in this position.

Tempus is committed to supporting the growth and career development of its employees, including Jr. Clinical Trials Data Specialists. By fostering a collaborative work environment and offering opportunities for skill development, team members can enhance their expertise and advance their careers within the company.

The work environment for a Jr. Clinical Trials Data Specialist at Tempus is fast-paced, energetic, and collaborative. Team members work together across various functions, making it an exciting place to grow and contribute to impactful research in cancer genomics.

Yes, Tempus provides comprehensive training programs for new hires in the Jr. Clinical Trials Data Specialist position. These programs are designed to help employees quickly learn and adapt to the company's workflows while ensuring they feel confident contributing to their teams.

Clinical trials are crucial to advancing cancer research as they evaluate new treatments and therapies. In your response, illustrate your knowledge of trial phases, types, and how they contribute to improving patient outcomes. Show your passion for their significance in the fight against cancer.

Highlight your ability to collaborate effectively. Provide an example where you contributed to a team, outlining your specific role and the outcome. Emphasize any challenges faced and how your communication skills helped overcome them.

In your answer, outline the specific quality control methods you apply, such as data validation techniques or checklists. Illustrate your attention to detail and the importance of maintaining data integrity in clinical settings.

Demonstrate your organizational skills and ability to manage time effectively. Discuss any tools or techniques you use to prioritize tasks and provide an example of a situation where this skill was vital to project success.

Share your passion for cancer research and genomics, tying in personal insights or experiences that fueled your interest. Discuss how being part of a team dedicated to making a difference excites you.

Emphasize your adaptability to remote work settings, your communication strategies for effective collaboration, and your experience with digital collaboration tools. Provide examples of successful remote team projects you've been involved in.

Discuss any relevant experiences where you've analyzed clinical records, emphasizing your analytical skills and attention to detail. If pertinent, tie in any academic or internship work as examples.

List relevant software programs or tools you've worked with, explaining how they relate to data analysis or clinical reporting. If you have experience with any specific platforms endemic to clinical trial data, mention that.

Share methods you use to keep current, such as following relevant publications, attending webinars, or participating in professional organizations. This demonstrates your proactive approach to continued learning in the field.

Discuss the importance of integrity and accuracy in reporting. Explain your approach to promptly address the error, including how you would inform team members and rectify the situation, showcasing responsibility and teamwork.