Research Associate - TIME

Posted 12 Days Ago
Easy Apply
Hiring Remotely in North East, PA
Remote
Mid level
Artificial Intelligence • Big Data • Healthtech • Machine Learning • Analytics • Biotech
Tempus is a data-driven precision medicine company bringing the power of data and artificial intelligence to healthcare.
The Role
The Research Operations Associate will manage key sites in the TIME clinical trials network, serve as the primary contact for research teams, draft and execute operational plans, collaborate with various teams, educate on clinical trial access, and oversee site support staff. Responsibilities include building client relationships, identifying resource gaps, and contributing to marketing and sales efforts.
Summary Generated by Built In

Tempus created the TIME clinical trials network to increase patient access to clinical trials by bringing the trial to the patient. The TIME program is an industry leader in the field of just-in-time (JIT) clinical trials.

We are looking for an experienced Research Operations Associate who will work with our cross functional team to manage key sites in the TIME research network. 

Responsibilities:

  • Primary point of contact for research teams/care teams for all matters related to TIME trial activities. 
    • Maintain a regular cadence of touch points (in person, virtual, emailing value adds) with targeted accounts (ie 2x per month per site)
    • Build relationships with key client stakeholders 
    • Draft and execute strategic operational plans, to ensure TIME sites can meet JIT standards. 
    • Oversight of all processes included in the above operational plan
    • Provide ongoing education to create awareness of access to a portfolio of clinical trials.
      • For all meetings where a MD is not present
    • Participate in research steering committees (where applicable)
      • Research Operations Director to delegate attendance to other research meetings where applicable. 
  • Collaborate with various teams within Tempus, to execute key deliverables including operations, clinical members (RN/MD), sales, medical affairs, pathology, bioinformatics and data science
    • Attend ISAMs (as delegated by ROD)
    • Attend TSAMs
  • Utilize knowledge of oncology, clinical trial development and study start-up to identify site resource gaps, and onboard sites into the systems. 
    • Assist/pull in a team to create innovative tactics, processes, tools, systems, and strategies to ease site burden/gaps in clinical trial participation.
    • Incorporate key client feedback into product and process improvements.
  • Contribute to the development of marketing and sales collateral.
  • Attend approved regional/local conferences (upon approval)
  • Administrative activities associated with the activities listed above
  • Oversight of site support staff as applicable (Program Coordinator)

Qualifications:

  • Regular travel required (up to 40%)
  • Bachelor's Degree and 3+ years of experience in working in oncology and/or clinical trials
  • Deep understanding of study start up.
  • Strong ability to persuade, be strategic, motivate, and influence others.
  • Proven track record of setting and achieving high personal standards of performance.
  • Highly organized and systematic, superb attention to detail and ability to complete tasks with a high degree of accuracy. 
  • Persistent and resilient with an ability to be a good listener.
  • Ability to develop and maintain strong relationships.
  • Advanced written and oral communication skills.
  • Superior analytical, interpersonal, and problem-solving skills.
  • Tenacious appetite for success.  
  • It is necessary to view and type on computer screens for long periods and to work in an environment which can be stressful due to heavy workload and frequent interruptions.




#LI-AW1#LI-Remote

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.


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.

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The Company
HQ: Chicago, IL
2,482 Employees
Hybrid Workplace
Year Founded: 2015

What We Do

Tempus is a technology company advancing precision medicine through the practical application of artificial intelligence in healthcare. With one of the world’s largest libraries of clinical and molecular data, and an operating system to make that data accessible and useful, Tempus enables physicians to make near real-time, data-driven decisions to deliver personalized patient care and in parallel facilitates discovery, development and delivery of optimal therapeutics.

The goal is for each patient to benefit from the treatment of others who came before by providing physicians with tools that learn as the company gathers more data. For more information, visit tempus.com.

Why Work With Us

We're looking for those who challenge the status quo. For the builders who are never done building and the learners who are never done learning. We're looking for unwavering commitment and undying curiosity. We're looking for the smartest people on the planet to attack one of the most challenging problems mankind has ever faced.

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Tempus AI Offices

Hybrid Workspace

Employees engage in a combination of remote and on-site work.

Most of the team follows a hybrid policy, with some roles allowing for a fully remote arrangement and some roles being onsite only.

Typical time on-site: 3 days a week
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