Raleigh, NC · On-site
$123.50K - $185K/yr
We focus on enabling efficient, collaborative, timely execution of clinical trials to make research ... Manage individual project priorities, deadlines and deliverables. * Collaborate with cross ...
Raleigh, NC · On-site
$123.50K - $185K/yr
We focus on enabling efficient, collaborative, timely execution of clinical trials to make research ... Manage individual project priorities, deadlines and deliverables. * Collaborate with cross ...
Boston, MA · On-site
$123.50K - $185K/yr
... manage their chronic health conditions and general health while participating in important clinical ... Verily Life Sciences LLC is an equal opportunity employer. Qualified applicants will receive ...
Boston, MA · On-site
$123.50K - $185K/yr
... manage their chronic health conditions and general health while participating in important clinical ... Verily Life Sciences LLC is an equal opportunity employer. Qualified applicants will receive ...
Boston, MA · On-site
$177.50K - $266K/yr
Staff Software Engineer At Verily, we're on a mission to make precision health a reality--and we're ... Ensure compliance by working closely with privacy, security, and quality teams, while managing ...
Boston, MA · On-site
$177.50K - $266K/yr
Staff Software Engineer At Verily, we're on a mission to make precision health a reality--and we're ... Ensure compliance by working closely with privacy, security, and quality teams, while managing ...
Dallas, TX · On-site
$134K - $190K/yr
Sr. IT Systems Engineer Verily is a subsidiary of Alphabet that is using a data-driven approach to ... We are focused on generating and activating data from a variety of sources, including clinical ...
Dallas, TX · On-site
$134K - $190K/yr
Sr. IT Systems Engineer Verily is a subsidiary of Alphabet that is using a data-driven approach to ... We are focused on generating and activating data from a variety of sources, including clinical ...
What are the key skills and qualifications needed to thrive as a Clinical Trials Manager, and why are they important?
What are some common challenges faced by Clinical Trials Managers and how can they be addressed?
What does a Clinical Trials Manager do?
What is the difference between Clinical Trials Manager vs Clinical Research Coordinator?
| Aspect | Clinical Trials Manager | Clinical Research Coordinator |
|---|---|---|
| Responsibilities | Oversees entire clinical trial process, manages teams, ensures compliance, and handles budgets. | Assists with patient recruitment, data collection, and site coordination under supervision. |
| Required Credentials | Bachelor’s or higher in life sciences, often with project management experience. | Typically holds a bachelor’s degree in health sciences or related field; certification may be preferred. |
| Work Environment | Works in clinical trial sites, research organizations, or pharmaceutical companies. | Primarily works at clinical sites, hospitals, or research facilities. |
In summary, Clinical Trials Managers oversee the entire trial process and manage teams, while Clinical Research Coordinators support daily trial activities at the site level. Both roles require relevant education and work in clinical research settings, but differ in scope and responsibilities.
$123.50K - $185K/yr
Other
This job post has expired today. Applications are no longer accepted.
Verily is working to advance precision health by closing the gap between research & care. The Viewpoint Site CTMS team is building the next generation of software for the clinical research site. We focus on enabling efficient, collaborative, timely execution of clinical trials to make research an enjoyable, cost effective endeavor. You will join an interdependent, fun, engaged development organization that is focused on delivering high-quality software solutions.
Are you ready to own all aspects of the software development life cycle? Is collaboration something you require in your next role? Are you biased towards taking action? Do you want to apply your skills towards making a difference in people's lives?
Agile isn't something we do, it's something we are! So if you are up for the challenge of solving real word problems working alongside a team of intelligent and driven individuals then we are ready for you!
What we work with:
Minimum Qualifications
Preferred Qualifications
Qualified applicants must not require employer sponsored work authorization now or in the future for employment in the United States.
The US base salary range for this full-time position is $123,500 - $185,000 + bonus + benefits. Our salary ranges are determined by role, level, and location. The range displayed on each job posting reflects the minimum and maximum target for new hire salaries for the position across all US locations. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific salary range for your preferred location during the hiring process.
Please note that the compensation details listed in US role postings reflect the base salary only, and do not include bonus or benefits.
Verily Life Sciences LLC is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If you have a need that requires accommodation, please let us know by completing our Accommodations for Applicants form.
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Biotechnology research and development
1,001 - 5,000 Employees
San Francisco, CA, US
2015