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26 results
June 1, 2016

Small biotech company is seeking a Medical Writing Consultant for a part- time (20 hours per week) 3 month contract opportunity. The work may be done remotely but this person needs to be available to come to the office during the week for meetings.
Responsible for writing protocols and investigator brochures. Hematology/oncology background is required.

June 1, 2016

The candidate will be responsible for implementing Phase 1-3 infectious disease vaccine or drug trials for a small biotechnology company in San Diego, reporting to the VP, Clinical Vaccines. Responsibilities include:
• Achieving U.S. Food and Drug Administration (FDA) standards for subject safety and data integrity.
• Managing a Contract Research Organization (CRO) in the conduct of clinical trial(s).
• Fostering effective and collaborative interactions among Clinical and Company employees and with the staff of multiple U....

April 4, 2016

Ionis Pharmaceuticals, Inc., located in the North San Diego County city of Carlsbad, was founded in 1989 to create advanced, novel medicines to treat complex and challenging diseases. We are the pioneer in the discovery and development of antisense drugs with more than 1300 patents.

Ionis is a challenging, motivating and rewarding environment designed to foster innovation and scientific excellence. Our founding goals have changed little in over 27 years and our success is a direct result of our outstanding employees. We are...

March 8, 2016

Typically serves as the Lead CRA (LCRA) with full responsibilities for clinical monitoring and line management of Clinical Research Associates (CRAs). Ensures appropriate communication, regulatory documentation, and ongoing oversight. Provides support for business development.

January 15, 2016

osition Summary:
The Clinical Trial Assistant provides clinical trial management support to the study team and is responsible for the development and maintenance of the Trial Master File.

January 15, 2016

Member of the clinical team responsible for conducting Phase I - IV studies according to Federal Regulations and ICH guidelines and study protocol, including planning study conduct, writing study protocols, designing CRFs, CRO selection, CRO training and management, selections and training of study investigators, planning and running study meetings, and overseeing the evaluation, selection and training of new study investigators. Responsible for the initial budget and contract negotiations with study sites or CROs. Responsible for writing...

January 15, 2016

(Non-Oncology trials)

Sr. CRA to help out on both a single site trial at Standford and a multi-site trial for a Small Sponsor (small team). Contract will be written in 6 month blocks. Please let connect to discuss some of the details we are not able to list online.
We have other sponsors with similar needs so lets connect so I am able to have a good understanding of your experience to better assist you.

Mohammad Ouranos| Clinical Recruiter
Advanced Clinical
570 Pacific Ave, San Francisco, CA 94133

January 15, 2016

Hope you are doing well. Please review the job opportunity below and contact me if you are interested or may know of someone interested.
Thank you in advance.

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 CTM/SR CTM to work within one of our leading pharmaceutical clients in South San Francisco, CA:
(Permanent, Contract, Consulting available for this role)



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