HEMA Health Economics and Market Access Processes Coordinator

Artech LLC

  • Cincinnati, OH
  • 2 days ago
  • Remote
  • $25–$29 Per Hour

Highlights

This role is located in Cincinnati Ohio and will operate under the direct supervision of the HEMA Research Operations Associate Director-- providing full-time (40 hours per week) process administration support. Client is the world's most comprehensive and broadly based manufacturer of health care products, as well as a provider of related services, for the consumer, pharmaceutical, and medical devices markets.

Numbers & Facts

LocationCincinnati, OH (
Remote
)
Salary$25–$29 Per Hour

Description

Title : HEMA Health Economics and Market Access Processes Coordinator
Location:Remote (Cincinnati; Ohio)
Duration : 12+ Months
Pay Range : $25-29/hr.
Part Time: 20 hours per week

HEMA Processes Coordinator

Caring for the world, one person at a time has inspired and united the people of Clients for over 125 years. We embrace research and science -- bringing innovative ideas, products and services to advance the health and well-being of people.

Client is the world's most comprehensive and broadly based manufacturer of health care products, as well as a provider of related services, for the consumer, pharmaceutical, and medical devices markets. Employees of the Client & Client Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world.

This role is located in Cincinnati Ohio and will operate under the direct supervision of the HEMA Research Operations Associate Director-- providing full-time (40 hours per week) process administration support.

Basic responsibilities

  • Administer the approval process of research protocols using PUBSTRAT, including basic quality control, according to standardize procedures
  • Administer the approval process of scientific publication submissions using PUBSTRAT, including basic quality control, according to standardized procedures
  • Maintain entries into research process trackers and summarization of information for reporting to senior leadership
  • Assist in development and updating/maintenance of PUBSTRAT administrators process guidelines
  • Serve as main point of contact with the vendor of the PUBSTRAT platform
  • Document Preparation: memorandums, correspondence, and/or presentations as needed.
  • File management (e.g., Client 365 Teams, SharePoint, Word, Adobe)
  • Assist in the critical review and proofread of standardize process documents
  • Assemble relevant data, generate reports, compile statistics or information as directed (as needed)
  • Conduct debarment/exclusion check
  • Assist in development and maintenance of training curricula in ComplianceWire
  • Flexibility to accommodate a changing work schedule and sensitivity to international time zones is required.
  • Develop in-depth knowledge of department s research processes, policies, and procedures
  • Acquire knowledge of department organizational structure
  • Collaborate with administrative staff colleagues to ensure office efficiencies
  • Maintain CLIENT Credo objectives
  • Assist with Purchase Order requests and processing
  • Provide other administrative support as assigned by the Associate Director.

Qualifications

  • A minimum of an associate degree is required. A bachelor s degree is preferred.
  • Experience with publication management systems (e.g., PUBSRAT, PubPro) is highly preferred
  • Basic understanding of research methodologies (in clinical/health preferred)
  • Knowledge in regulatory and/or compliance in health care industry (e.g., clinical research, trials, health outcomes research) is highly preferred
  • Basic understanding of scientific publication methodologies preferred
  • Proficiency in Client Office (Word, Excel, PowerPoint, Outlook, Adobe) is required
  • Ability to learn specialized computer (or Web-based) software used for document approval processes, training curricula, and other applications
  • Prior experience with creating standardized operating procedures is preferred
  • Must have excellent time management skills
  • Must have good verbal and written communication and interpersonal skills
  • Must have strong organizational skills, along with excellent judgment and reasoning abilities.
  • Must be a strong team player with the ability to coordinate with other HEMA associates and research partners
  • Ability to multi-task and work under minimal supervision, in a dynamic, fast-paced, multicultural, international environment is required.

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