Clinical Research Associate I

South San Francisco, CA 94080

Posted: 09/18/2018 Employment Type: Contract Industry: Clinical & Scientific Job Number: 13880

Bayside Solutions is seeking a Clinical Research Associate I to be part of our client’ s team in South San Francisco . This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Clinical Research Associate I:

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Communicate with internal team members and Contract Research Organizations (CROs) regarding trial start-up, maintenance, and close-out activities.
  • Work in collaboration with the Clinical Study Manager (CSM) assists in the oversight of vendor activities along with the CROs.
  • Receive regulatory documents for review and submission to the Regulatory Department.
  • Develop Trial Master File (TMF) plan and manage through transfer of documents to the Sponsor.
  • Provides guidance with development of the clinical trial binders for study sites.
  • Manage and track study-specific payments and invoices.
  • Provide support for investigator meeting planning, including organizing meeting materials and provide on-site meeting assistance (as needed).
  • Oversee CRO tracking systems and tools to support the conduct of a clinical trial from start-up to close-out phase.
  • Provide support to CSM on start-up activities.
  • Review and collaborate with CSM on the development of certain study specific plans and/or processes (e.g. Satellite Site Management Plans or Drug Destruction Memos).
  • Collaboratively work with CRO to ensure CTMS has current updated information.
  • Manage and track vendor-specific payments and invoices.
  • Assist with maintaining tracking and reporting of study metrics.
  • Coordinates with Clinical Study Manager (CSM) to communicate relevant trial information between various internal functional members and contract vendors.
  • Manage tracking and delivery of clinical/ non-clinical supplies.
  • Generate and review trial management reports from internal tracking systems at requested intervals.
  • Conduct timely review of clinical trial documents upon request.
  • Review Informed Consent documents as well as Monitoring Visiting Report Review (PSSV, SIV, IMV and COV).
  • Provide support to both internal and external departmental members when necessary.
  • May serve as subject matter expert on task forces, initiatives, and working groups.

Summary of Qualifications:
  • Bachelor’ s degree or equivalent required.
  • A minimum of 5 years in clinical research, or health related industry required.
  • Highly effective verbal and written communication skills; effectively delivers key messages’ aptitude to independently communicate with teams and stakeholders.
  • Demonstrates an aptitude to distill information from multiple sources to create meaningful insights and induces collaboration and innovative thinking study-wide.
  • Experience with effective vendor management preferred.
  • Demonstrates an aptitude for strategic thinking skills; manages risks (including risk identification and mitigation); identifies critical path/critical dependencies.
  • Strong customer focus with functional peers, vendors, country affiliates, etc.
  • Excellent planning and organizational skills.
  • Ability to build trusting and collaborative relationships that promote innovation, knowledge-sharing and adaptation to change.
  • Practices the ability to influence and negotiate to achieve team goals.
  • Consistently supports change in an effort to continue to develop USMA’ s dynamic organization.
  • Demonstrates creativity and innovation to support projects and initiatives.
  • Strong technical and analytical skills and ability to manage system data maintenance across multiple systems.
  • Aptitude to interpret outputs from analytical tools to enhance and improve study execution.
  • Self-motivated, achievement-driven and exhibits ability to work with minimal guidance. 

Elizabeth Isabel

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