Back to List

Support Scientist I- Study Coordination

Req ID #: 220185

Cleveland, Ohio, USA

About this job

We are seeking a Support Scientist I, Study Coordination for our Manual Ion Channel Testing Team at our Safety Assessment site located in Cleveland, OH.

We are seeking a Support Scientist I, Study Coordination for our Manual Ion Channel Testing Team at our Safety Assessment site located in Cleveland, OH.

Support Scientist provides administrative and scientific support to the Project Scientists/Study Directors.  Staff participate in the tracking and managing study related materials, providing requested data/information to the Project Scientist/Study Director or Sponsor, interpreting, and reporting study related data, and contributing to the improvement and optimization of the discipline workflows.  Staff are also knowledgeable in the application of GxP’s and applicable SOPs, along with adhering to study protocols where required.

Essential Functions (The fundamental Competencies/Skills & Responsibilities of the role (products and services provided/results accomplished) include, but are not limited to, those listed: 

  • Efficiently perform and document all procedures, materials and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.)

  • Accurately review study data for adherence to SOPs, methods/protocols and regulatory requirements

  • Effectively complete administrative tasks such as filing and placing orders as needed

  • Ensure documents align with requirements indicated in Client Information Database (CID)

  • Attain CRL personnel and Sponsor signature/approval for study documents and distribute documents when necessary

  • Attend study and/or department related meetings to assure understanding of assigned projects

  • Demonstrate effective communication skills through informal discussions with peers, supervisor, team and Sponsor/SDs

  • Develop critical thinking, troubleshooting and time management skills aligned with needs of operational areas

  • Maintain department, study and inventory trackers in support of Project Scientist/Study Director

  • Assist in preparation of data shared with Sponsors

  • Efficiently perform daily operational tasks to support the Project Scientist and Laboratory staff within one operational area

  • Assist with generation and maintenance of standard draft study plans/protocols/amendments and reporting templates in accordance with CRL or Sponsor specific

  • Perform all other related duties as assigned

The pay for this position is $23.00/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location

CRL site

About Charles River

Charles River is an early-stage Contact Research Organization (CRO). Here, we are passionate about our role in improving the quality of people's lives. With 100 sites around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our clients' unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.

Learn More