Review Process Lead in US-Remote

  • Title: Review Process Lead
  • Code: RCI-68493
  • RequirementID: 120418
  • Location: US-Remote
  • Posted Date: 08/19/2024
  • Duration: 1-2 Months
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  Job Description

Notes from Manager:

  • Role will be Remote, should be in EST time zone
  • The manager is not sure if this will last longer than 2-3 months
  • Must have a Bachelors Degree in a General Science field
  • Must have prior exp with Patient Recruitment and Retention
  • Will use Veeva Platform
  • Contractors will get emails from recruitment teams (not sourcing)
  • Will be responsible for routing material to appropriate people in company
  • Will be tracking work flows
  • Will be responsible for data for weekly meetings
  • Must be able to take care of action items
  • Will be working with material for Clinical Trials
  • Must have at least 3 years of exp
  • Must have exp with MS Office & SharePoint

 

Top 3 Criteria:

  • Patient Recruitment experience
  • Must be detailed oriented
  • Experience with Veeva platform

 

Duties:

  • The position is primarily accountable for driving the internal compliance review of patient and retention tactics.
  • This position acts as the interface with Regulatory Advertising and Promotion (RAP), Privacy, Health Care Compliance Officers (HCCOs), Law Department, study team members, suppliers, and other stakeholders involved in the development, management, and dissemination of patient and site-facing tactics.
  • This position is responsible for maintaining documentation of business processes and quality standards for effective compliance submissions.

 

Education/ Experience:

  • Bachelor’s Degree or equivalent, preferably in a scientific or health-related discipline.
  • At least 3 years of relevant experience in global patient recruitment, clinical trial execution with a pharmaceutical company, CRO, and/or healthcare facility/research site.
  • Expertise in the areas of drug development, clinical trial operations, and strategic planning.
  • Previous experience in clinical trial operations including the execution of study outreach, patient compliance and study support programs.
  • Strong planning and tracking skills, customer focused, well organized, detail oriented and capable of successfully managing multiple projects.
  • Excellent time, priority, and self-management skills.
  • Strong project management skills.
  • Strong team orientation: demonstrates initiative to solve problems and improve efficiency and/or customer service.
  • High degree of proficiency in Microsoft Excel, PowerPoint and Word.
  • Microsoft Project, Veeva preferred.


About Rangam:

Rangam Consultants is a minority, women-owned, disability workforce solutions global organization. Specialized in attracting and retaining talents globally for a rewarding career in IT, Engineering, Scientific, Clinical, Healthcare, Administrative, Finance, Business Management, and many more, while integrating veterans and individuals with disabilities into the workforce. Indeed, we connect career aspirants to relevant job opportunities, be it jobs in USA, UK, India, or Ireland. Also remote jobs, work-from-home jobs, or contract jobs in different verticals and industries.
Rangam strives to put job seekers first, giving them free access to search for jobs, post resumes, and research companies.Every day, we connect millions of people to new opportunities.