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26 results
October 3, 2016

Title: Associate Director/Director (depending on experience)
Company: Small Biotech
Location: San Diego, CA (must work in the office)
Target Salary: TBD
Travel: Very limited
Requirements: 8+ years of experience in clinical research. Will look at candidates at the Sr. Project/Trial Management level who are ready to take the next step. Must have experience working on EU trials. Ideally candidates will have experience at both a CRO and a small sponsor company. Must have experience with Phases I-IV and have the...

July 30, 2016

Sponsor is a clinical-stage, cancer-selective gene therapy company focused on developing first-in-class, broadly applicable product candidates designed to activate a patient’s immune system against their own cancer from within.

Every member of our team plays a significant role in our success. Sponsor hires individuals who share our passion for ending cancer mortality and have exceptional talent that will contribute to this goal.


The Clinical Study Manager will be responsible for the conduct of clinical...

June 29, 2016

A Clinical Research Associate (CRA) job in San Diego, CA needs to be filled immediately by Adecco Medical & Science. This is a direct hire opportunity. In this position you will perform and coordinate all aspects of the clinical monitoring and site management process in accordance with ICH E6 Good Clinical Practices, FDA guidelines, local regulations and standard operating procedures. Additionally, you'll be responsible for performing the clinical monitoring aspect of designated projects in accordance with applicable SOPs; performing...

June 20, 2016

The candidate will be responsible for all aspects of clinical site management, regulatory compliance, and documentation requirements related to site qualification, initiation, routine monitoring, and close-out visits. Responsibilities will include maintaining frequent contact with and working effectively with clinical site staff, preparing and tracking required documentation from clinical sites, and assuring regulatory compliance with corporate SOPs, FDA, and ICH guidelines. The candidate will also assist clinical operations management...

June 6, 2016

The CRA will report to the Assistant Director of Clinical and Regulatory Operations and is responsible for assisting with the design, administration, and monitoring of clinical trials; monitoring and managing clinical data from collection through locked database; and ensuring compliance with clinical protocols, their objectives, and ICH and GCP guidelines.
Responsibilities and Duties:
• Assist with the design of clinical studies.
• Coordinate investigational site startup activities including, but not limited to, the...

June 6, 2016

Sr. Clinical Research Associate
- 2 month full time contract - will be office based with some travel

If interested, contact:

Natalie Duner

Real Life Sciences
Desk Hub, 2159 India Street, Suite 200, San Diego, CA, 92101, United States
T: +1 619 881 0004

June 3, 2016

Advanced Clinical is a global, clinical outsourcing organization built around delivering a truly better clinical trial experience. We have a great job opportunity for a Sr CRA’s to support one of our pharmaceutical clients:

Several needs coming up so will keep you posted on the additional details that will start coming in soon. Please let me know if you are interested and available in the coming weeks. (or if you know of someone else that would be interested/available.)
1099 $85/HR (door-to-door)
Interview process to...

June 2, 2016

This position will be responsible for conducting site visits, including pre-study, initiation, monitoring and termination; Ensuring adherence to all FDA, ICH-GCP and local regulations and Ensuring the completion and collection of regulatory documents.

If interested, please contact:

Joby Fernandez, Senior Recruiter. Sterling Life Sciences, a Division of Sterling-Hoffman Executive Search.


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Best Practices for your Clinical Trial

Are you aware of the latest regulations? One thing you can count on with our industry is that regulations are always updated and can be complex. Don’t worry! You can find all the information you need right here. (It’s stil up to you to read all of it though...)


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