Clinical Trial Assistant (CTA)
Clinical Trial Assistant (CTA)
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Salary Not Disclosed
1 Vacancy
Job Description
Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The companys R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins and RAS Companion Inhibitors for use in combination treatment strategies. As a new member of the Revolution Medicines team you will join other outstanding Revolutionariesin a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.
The Opportunity:
This is a unique opportunity for an entry-level Clinical Operations Professional. As a Clinical Trial Assistant (CTA) you will be responsible for providing administrative and operational support for one or more studies within a clinical program. Reporting into the Sr. Clinical Program Manager you will play a critical role in executing well-defined tasks that support clinical study start-up maintenance and close-out.
Responsibilities:
Work on assignments and problems of limited scope requiring independent decision-making and initiative using standard procedures under close supervision.
Solicit Clinical Study Execution Team (CSET) meeting agenda topics coordinate meetings minutes and logistical support.
Support site management activites and provide status to CSET (e.g. tracking site documents distributing study materials site enrollment metrics etc.).
Liaise with internal teams and vendors for document collection and update; act as primary CTA contact on studies.
File study documents to the Trial Master File (TMF) and assist with TMF reviews. Maintain TMF and ensure document quality and completeness.
May assist with protocol amendment documentation and version control.
May assist with development of basic department initiatives process documents and standard forms most used by CTAs.
Support other clinical operations activities as appropriate.
Required Skills Experience and Education:
BS BA or RN in a relevant scientific discipline.
0-3 years of relevant experience in the pharmaceutical or biotech industry preferably in Clinical Operations or Clinical Research related experience.
Basic understanding of FDA and EMA Regulations ICH guidelines GCP and familiarity with standard clinical operation procedures (SOPs).
Basic organization and communication skills.
Proficient in MS Office (Word Excel Outlook) and project tracking tools.
Demonstrate reliability proactive communication and quality in task execution.
Apply knowledge of Clinical Operations in day-to-day assigned tasks.
Thrive in a collaborative team setting and be driven by a desire to deploy innovative approaches and technologies in a high-energy environment.
Travel may be required (10%).
Preferred Skills:
Has familiarity working with vendor systems/portals (e.g. eTMF EDC IRT CTMS).
Oncology experience preferred. #LI-Hybrid #LI-JC1
The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role level and location. Individual base pay salary is determined by multiple factors including job-related skills experience market dynamics and relevant education or training.
Please note that base pay salary range is one part of the overall total rewards program at RevMed which includes competitive cash compensation robust equity awards strong benefits and significant learning and development opportunities.
Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race color religion gender sexual orientation gender identity/expression national origin/ancestry age disability marital status medical condition and veteran status.
Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect process and use any personal data that you provide to us in accordance with ourCCPA additional information please contact.
Employment Type
Full Time
