Process Coordinator

1 week ago

Cincinnati, Ohio, United States Integrated Resources Full time
Integrated Resources, Inc

Cincinnati, OH (Onsite)

Full-Time
Company is currently recruiting for a Casual Full-Time Health Economics and Market Access (HEMA) Process Coordinator.
Caring for the world, one person at a time has inspired and united the people 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 Company work with partners in health care to touch the lives of over a billion people every day, throughout the world.


Pay range:
$29.50/hr on w2.

Job Description:
Company is currently recruiting for a Casual Full-Time Health Economics and Market Access (HEMA) Process Coordinator.
Caring for the world, one person at a time has inspired and united the people 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 Company 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., Microsoft 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 checks.
Assist in development and maintenance of training curricula in Compliance Wire
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 Pharmaceutical 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 Microsoft 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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