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Clinical Research Associate II

Systimmune

Role overview

Qualifications

  • Bachelor’s degree in health science or related field
  • 2+ years monitoring Oncology trials independently conducting on-site and remote monitoring visits
  • Excellent verbal and written communication skills required
  • Excellent organizational, multi-tasking and time management skills required

Responsibilities

  • Perform Site Evaluation Visits, Site Initiation Visits, Interim monitoring visits and Close Out Visits
  • Prepare the study reference manual, including liaising with the Contract Research Organization (CRO) team
  • Responsible for ensuring investigator sites have met all contractual and regulatory requirements for site initiation
  • Manage patient recruitment strategies, proactively identifying barriers to recruitment while proposing solutions

Key facts

Hard skills

Clinical Research Data Management Clinical Trials gRPC Site Assessment Continuous Monitoring Patient Referral Electronic Data Capture (EDC) Organizational Structure

Other skills

  • Microsoft Office
  • Communication
  • Multitasking
  • Time Management

About the company

Systimmune logo

Systimmune

Biotechnology

Located in Redmond WA, founded in 2014, Systimmune Inc. is a bio-pharmaceutical company focused on the treatment of cancer through developing novel therapeutic bi-specific, and tri-specific antibodies, as well as antibody-drug conjugates (ADC's). Our objective is to create biologics that work through systematic intervention on the solid tumor micro-environment, to either directly attack the tumor and/or to activate the immune system to attack the tumor. We are a group of highly experienced immuno-oncology scientists utilizing several technology platforms to develop world class advanced antibody-based drug therapies.

Company details

IndustryBiotechnology
Company size51 - 200

Links

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Job description

SystImmune is seeking a high quality, ambitious and experienced Clinical Research Associate II (CRA II) to support SystImmune’s clinical trials.   The CRA II is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP guidelines, local regulations, and applicable SOPs.  The CRA II must be self-motivated, independent, and able to work in a small team environment. The successful candidate will be a highly organized individual who can also multitask and adjust direction based on changing project/corporate priorities.

Job Responsibilities:
  • Perform Site Evaluation Visits, Site Initiation Visits, Interim monitoring visits and Close Out Visits
  • Prepare the study reference manual, including liaising with the Contract Research Organization (CRO) team (i.e., central lab, specialty labs and vendors) to ensure efficient preparation and delivery of study materials to investigator sites
  • Responsible for ensuring investigator sites have met all contractual and regulatory requirements for site initiation and first release of study drug
  • Assist in the development of study/program plans (i.e., Monitoring Plan, eCRF Completion Guidelines, Data Management Plan, Safety Management Plan, etc.)
  • Manage patient recruitment strategies, proactively identifying barriers to recruitment while proposing solutions (i.e., study-site webinars, newsletters or other potential creative solutions)
  • Monitor recruitment, data quality and patient safety while on site and remotely through EDC systems and direct site communication
  • Liaise with study site personnel to ensure timely and correct entry of data into eCRF, including the timely resolution of data queries
  • Maintain project files including ethics committee approvals, curricula vitae of investigators and study personnel, clinical investigators brochure, protocols, case report forms instructions, consent documents, clinical-trial material shipping orders, start-up meeting attendance documentation, letters of agreement, lab reference ranges, and all investigator and site correspondence
  • Identify and complete follow- up of SAEs at study sites
  • Assist with data listing, data coding, patient profile reviews, database lock, and site close-out activities
  • Ensure appropriate and timely submission of documents to the Trial Master File
  • Perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/patients according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP. 
Qualifications: 
  • Bachelor’s degree in health science or related field.
  • 2+ years monitoring Oncology trials independently conducting on-site and remote monitoring visits.
  • Excellent verbal and written communication skills required.
  • Excellent organizational, multi-tasking and time management skills required.
  • Demonstrated experience developing/maintaining site relationships and securing compliance
  • Working knowledge of International Conference on Harmonization Good Clinical Practice guidelines
  • Experienced in Microsoft Office Products (Word, Excel, PowerPoint, SharePoint, Teams) and other clinical trial systems (e.g., CTMS, EDC and eTMF)
  • Ability to travel as required (50-75%)
Compensation and Benefits:

The expected base salary range for this position is $80,000 - $110,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s qualifications, experience, and skills.
 

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Marcus Rivera

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