Remote Clinical Research Specialist

Integrated Resources INC·Remote(United States)
Healthcare
Excel

WFA Digital Insight

The remote job market has seen a significant surge in demand for clinical research specialists, with a reported 25% increase in job postings over the past year. As the healthcare industry continues to evolve, the need for skilled professionals to manage clinical trials has become more pressing. Integrated Resources INC stands out in this space, offering a unique opportunity for remote work and professional growth. With the rise of telehealth and digital trials, the skills required for this role, such as Excel proficiency and attention to detail, are in high demand. Candidates should be prepared to demonstrate their knowledge of GCP and SOPs, as well as their experience in managing clinical trial databases and tracking tools.

Job Description

About the Role

As a Remote Clinical Research Specialist at Integrated Resources INC, you will play a critical role in managing clinical trials and supporting sites globally. This role entails working closely with study teams to ensure compliance with GCP and SOPs, as well as coordinating the logistics of clinical trials. You will be responsible for arranging and participating in study team meetings, taking minutes, and distributing meeting materials.

The ideal candidate will have a strong understanding of clinical trial management, including the randomization process, IWRS administration, and study document management. You will be working remotely, with occasional on-site visits required for training and meetings.

What You Will Do

  • Provide product training and support to clinical sites for the pill cam procedure
  • Support the randomization process and act as the IWRS PRIMARY Administrator
  • Arrange and participate in the organization of study team meetings
  • Take minutes and distribute meeting materials
  • Manage and maintain study documents and trial supplies, including colonoscopy forceps and FedEx envelopes
  • Administer, maintain, and coordinate the logistic aspects of clinical trials according to GCP and SOPs
  • Ensure that any clinical trial databases/tracking tools are set up and maintained throughout the trial
  • Assist with collating, tracking, and shipping CRFs and data queries to data management
  • Maintain study data control table and review and approve monitoring reports in Siebel CTM SW
  • Coordinate archiving of study documentation and perform and support study site qualification, initiation, interim monitoring, and closeout visits

What We Are Looking For

  • Bachelor's degree in Engineering, Life Sciences, or a related field
  • 0-2 years of experience in clinical research, preferably in a remote or decentralized trial setting
  • Strong understanding of GCP and SOPs
  • Proficiency in Excel and experience with clinical trial management systems
  • Excellent communication and organizational skills
  • Ability to work independently in a remote setting
  • Strong attention to detail and ability to maintain accurate records

Nice to Have

  • Experience with IWRS administration and randomization processes
  • Knowledge of Siebel CTM SW and other clinical trial management systems
  • Certification in clinical research or a related field
  • Experience with clinical trial database management and tracking tools

Benefits and Perks

  • Remote work arrangement with occasional on-site visits
  • Competitive salary and benefits package
  • Opportunity for professional growth and development in a dynamic and evolving field
  • Collaborative and supportive team environment
  • Access to cutting-edge technology and training resources
  • Flexible working hours and work-life balance

How to Stand Out

  • Tip: Make sure to highlight your experience with clinical trial management systems and your understanding of GCP and SOPs in your application.
  • Familiarize yourself with the company's specific clinical trial management software and be prepared to ask questions about their systems and processes.
  • Create a portfolio that showcases your experience in managing clinical trials, including any relevant certifications or training programs.
  • Be prepared to discuss your experience with remote work and how you stay organized and motivated in a decentralized setting.
  • Don't be afraid to ask about opportunities for professional growth and development within the company.
  • Consider reaching out to current or former employees to gain insight into the company culture and values.

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