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Senior Clinical Trial Associate - Remote / Hybrid Options (San Diego)

Company: Avidity Biosciences, Inc.
Location: Houston
Posted on: January 16, 2022

Job Description:

Avidity Biosciences, based in San Diego, is pioneering a new class of oligonucleotide-based therapies called AOCs designed to overcome the current limitations of oligonucleotide therapies -in order to -treat a wide range of serious diseases. We utilize our proprietary AOC platform to design, engineer and develop therapeutics that combine the tissue selectivity of monoclonal antibodies (mAbs) and the precision of oligonucleotide-based therapies -in order to -access previously undruggable tissue and cell types and more effectively target underlying genetic drivers of diseases. We are passionate about the impact of every employee in bringing these potentially transformative therapeutics to patients in need. Make a difference with us. -Job Summary
The Sr. CTA -is responsible for supporting the daily workflow of clinical operations activities. The Sr. CTA -provides administrative support to -study -teams throughout the -study, serves as a mentor and coach for other CTAs, as applicable. -Key administrative activities -include, but are not limited to, -managing meeting invitations, creating agendas -and meeting minutes, study document filing, -maintaining study trackers, -and oversight of the study-specific eTMF. -Essential Duties and Responsibilities -(including but not limited to):

  • Serves as a member of the -clinical -operations -team and provides administrative support -and tracking -of trial status, -with the goal to contribute towards efficient management of trials
  • Leads the onboarding effort for -the -eTMF
  • Responsible for the set up and maintenance of the -electronic -Trial Master Files -(eTMF) -according to eTMF Plan
  • Responsible for the collection of essential documents
  • Performs -quality control of the documents/files as per study milestones outlined in the project plan and with CTM (or designee) oversight
  • Collaborates with the -clinical -study -team -(internally and external CROs), under the direction of the CTM -(or designee), to ensure that the -eTMF is audit/inspection ready
  • Provides administrative support to the -clinical -study -team for study related activities (e.g. -maintenance of study mailbox, -newsletter creation/review, -study document formatting, binders, meeting minutes etc.)
  • Assists -CTM (or designee) and cross-functional leaders -in the production of various study reports and updates -i.e. -country/site initiation, activation; recruitment) t
  • Assists in planning -and -organizing project-specific meetings including but not limited to -internal clinical study team -meetings, -external service
  • provider/partner -meetings, -CRA training, Investigator Meeting and PI meetings. Creates agendas, meeting minutes, and distributes.
  • May act as point of contact for -study-related requests for team members and -service providers/partners
  • May assist with study start-up -activities, -including feasibility, investigator recruitment, and general site management support under CTM -(or designee) -oversight
  • May support the distribution and tracking of IND Safety Reports/SUSARS/CIOMS according to the procedures defined by the study team in the project plan
  • May coordinate the distribution and the reconciliation of study material (Operations Manual, ISF, patient cards, etc.) as required by the study
  • May support financial tasks for the study (e.g. -investigator/institution/vendors payments), coordinating tracking
  • May review, validate, track and file the essential documents for investigational sites as well as follows-up on missing/incomplete/invalid documents
  • May lead -other -CTAs to oversee QC process of -eTMF per project plan
  • Performs other duties as assigned by management -Qualifications -Minimum Required:
    • Graduate of a secondary education or equivalent degree
    • Minimum of -3 -years of clinical research experience or proven competencies for this position -Other Required:
      • Must have established experience and fluency in the Microsoft Office package of programs (Outlook, Word, -Excel -and PowerPoint)
      • Excellent organizational skills, attention to detail, and a customer service demeanor
      • Ability to speak English proficiently
      • Ability to travel domestically and internationally including overnight stays -Preferred:
        • Experience as a CTA
        • University degree preferred -Competencies:
          • Demonstrates a working knowledge of ICH/GCP and -clinical research processes
          • Solid working knowledge -and experience utilizing an -eTMF platform(s)
          • Demonstrates professionalism, as evidenced by punctuality, ability to deliver on commitments, possess good interpersonal skills and maintain positive interactions with internal and external stakeholders
          • Communicates both verbally and in written form in an efficient and professional manner
          • Demonstrates values and -a -work ethic consistent with -Company -Values
          • Exhibits high self-motivation, is detail-oriented, -and able to work and plan independently as well as in a team environment
          • Ability to develop, coach and mentor CTA staff
          • Focuses on continuous improvement, including the ability to make proactive assessments on how to make processes more efficient

Keywords: Avidity Biosciences, Inc., Houston , Senior Clinical Trial Associate - Remote / Hybrid Options (San Diego), Healthcare , Houston, Texas

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