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Jr. Clinical Trials Data Specialist at Tempus

Remote:

Full Remote

Contract:

Full time

Experience:

Junior (1-2 years)

Work from:

Illinois (USA), United States

Offer summary

Qualifications:

BS degree in Genetics, Molecular Genetics, Cancer Biology or Biological Sciences, Willingness to be flexible, Ability to learn and adapt quickly, Excellent communication skills, Excitement for a fast-paced environment.

Key responsabilities:

Collaborate within cross-functional teams to create customized clinical reports
Analyze patient records and testing results for trials
Perform quality control in clinical report workflow
Support ongoing and future team projects
Adjust priorities according to workflow needs

Tempus Biotech: Biology + Technology Unicorn https://www.tempus.com/

1001 - 5000 Employees

See more Tempus offers

Job description

Passionate about making a difference in the world of cancer genomics?

Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.

With the advent of genomic sequencing, we can finally decode and process our genetic makeup. We now have more data than ever before but providers don't have the infrastructure or expertise to make sense of this data. We're on a mission to connect an entire ecosystem to redefine how genomic data is used in clinical settings. We are looking for a Jr. Clinical Trials Data Specialist who will work with our cross-functional teams on clinical and research initiatives.

Responsibilities:

Works collaboratively within cross-functional teams at Tempus (including but not limited to scientists, pathologists, product development, etc.) to create customized clinical reports.
Analyze patient clinical records and molecular testing results to identify potential clinical trials.
Perform critical quality control functions in clinical report workflow.
Support ongoing and future projects within the team.
Ability to quickly adjust priorities according to workflow or business needs

Qualifications:

Minimum of a BS degree in Genetics, Molecular Genetics, Cancer Biology, or Biological Sciences.
Willingness to be flexible.
Ability to learn new skills quickly and adapt to new processes smoothly.
Excellent communication skills with the ability to work both independently and in a group setting.
Excitement and drive to make a difference in a fast-paced energetic work environment.

Preferred Qualifications:

Hematology/oncology knowledge.
Experience reading and critically evaluating clinical trials.

We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

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Additionally, for remote roles open to individuals in unincorporated Los Angeles – including remote roles- Tempus reasonably believes that criminal history may have a direct, adverse and negative relationship on the following job duties, potentially resulting in the withdrawal of the conditional offer of employment: engaging positively with customers and other employees; accessing confidential information, including intellectual property, trade secrets, and protected health information; and appropriately handling such information in accordance with legal and ethical standards. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law, including the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.