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Senior Clinical Trial Assistant (Open to Remote)

Employer
Global Blood Therapeutics
Location
Working from Home
Start date
Aug 5, 2022

View more

Discipline
Clinical, Clinical Research, Clinical Trials
Required Education
Bachelors Degree
Position Type
Full time
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Job Details

SENIOR CLINICAL TRIAL ASSISTANT (Open to Remote)

Position Summary:

The Senior Clinical Trial Assistant (CTA) is responsible for providing support to the lead Clinical Trial Manager (CTM) and Clinical Research Associate (CRA) in the management of clinical trials.

The Sr. CTA will be responsible for tracking and document maintenance as applicable and supporting the oversight of vendors and clinical trial sites. The Sr. CTA will work closely with a cross-functional team to ensure that clinical trials are conducted in a timely fashion and in compliance with GBT SOPs, ICH/GCP/regulatory guidelines, company goals and budgets.

Essential Duties and Responsibilities: 

  • Support one or more study execution team (SETs), including scheduling meetings, distributing agendas and meeting minutes
  • Document outstanding action items with expected completion dates and responsible individual(s).  Follows-up on all SET action items
  • Support SET risk management discussions, follow-up and documentation
  • Track and maintain study information and report on study progress
  • Track and provide IRB/IEC submission documentation and other supplementary documentation, as appropriate
  • Obtain, review, process, and track study related documents (CVs, FDA 1572s, lab certifications, IRB approvals, contracts, protocols, etc.)
  • Maintain and disseminate basic study tracking information including, but not limited to: visit reports, regulatory documents, site contact lists, team contact lists and vendor lists
  • Lead Essential Document Packet review and approval process
  • Lead ICF development, review and approval process
  • Attend monitoring oversight visits with CRA or CTM, where needed and as appropriate
  • Maintain and ensure the completeness of the Trial Master File (TMF) in accordance with SOP requirements
  • In collaboration with Supply chain, lead the management and tracking Investigational Product (IP)supplies for study sites
  • Oversight of preparation, shipment and management of study supplies to sites
  • Support preparation of materials for investigator meetings, workshops, and study manuals
  • Lead development of study newsletters
  • Lead onboarding of new CTA team members
  • Identify and support process improvement initiatives
  • All work must adhere to ICH Good Clinical Practice (GCP) guidelines and comply with company SOPs

Qualifications:

  • Bachelor’s degree or equivalent or combination of relevant experience and training
  • 2 to 4 years of relevant industry experience
  • Effective communication skills
  • Excellent organizational skills and attention to detail
  • Excellent problem-solving skills
  • Ability to efficiently perform multiple tasks and manage changing priorities
  • Appropriate and timely escalation
  • Ability to complete activities with minimal oversight
  • Demonstrate proficiency in Microsoft Word, PowerPoint and Excel
  • Take direction well

Fit with GBT culture:

  • Ability to build strong relationships with co-workers of various backgrounds and expertise
  • Ability to function at a high level in a team setting whether leading the group or acting as an individual contributor
  • Values-based leadership consistent with GBT's Core Values
  • Excitement about the vision and mission of GBT
  • Flexibility
  • Integrity

NOTE:  This position summary is not intended to be all-inclusive. Employee may perform other related duties as negotiated to meet the ongoing needs of the organization.

The Company complies with all laws respecting equal employment opportunity and does not discriminate against applicants with regard to any protected characteristic as defined by federal, state, and local law.  This position requires you to work onsite at the Company’s facilities.  The Company requires all employees working in its facilities (including attending in-person meetings and events) to be fully vaccinated from COVID-19 (except as required by applicable law).  Therefore, this position requires you to be fully vaccinated from COVID-19, subject to reasonable accommodations for a disability/medical condition or sincerely-held religious belief, and/or as otherwise required by applicable law.  The Company considers you fully vaccinated once 14 days have passed since you received either the second dose in a two-dose COVID-19 vaccine series or a single-dose COVID-19 vaccine. This position requires you to maintain a fully-vaccinated status against COVID-19, subject to reasonable accommodations required by applicable law. The vaccine must have been FDA approved, have emergency use authorization from the FDA, or, for persons fully vaccinated outside of the U.S., be listed for emergency use by the World Health Organization.

 

Company

Global Blood Therapeutics (GBT) is a biopharmaceutical company dedicated to the discovery, development and delivery of life-changing treatments that provide hope to underserved patient communities. Founded in 2011, GBT is delivering on its goal to transform the treatment and care of sickle cell disease (SCD), a lifelong, devastating inherited blood disorder. The company has introduced Oxbryta® (voxelotor), the first FDA-approved treatment that directly inhibits sickle hemoglobin polymerization, the root cause of SCD. GBT is also advancing its pipeline program in SCD with inclacumab, a p-selectin inhibitor in development to address pain crises associated with the disease. In addition, GBT’s drug discovery teams are working on new targets to develop the next generation of treatments for SCD. To learn more, please visit www.gbt.com and follow the company on Twitter @GBT_news.

Find Us
Website
Location
181 Oyster Point Blvd
South San Francisco
California
94080
United States
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