Resource Coordinator II

Posted 7 Days Ago
Be an Early Applicant
Hiring Remotely in São Paulo, BRA
In-Office or Remote
Mid level
Biotech
The Role
Manage a centralized resource management mailbox, route resource requests, execute weekly Excel allocation uploads, publish reports to SharePoint, and load baseline resource requests into a resource management tool. The role requires Excel data manipulation, clinical trial process knowledge, cross-functional communication, deadline management, and continuous process improvement in a matrixed pharmaceutical or CRO environment.
Summary Generated by Built In

Job Overview:

Cross business communication of resource requests that come from the centralized resource management mailbox. Required to interpret emails that come in from a centralized mailbox, determine where they should be routed. There are functional areas where daily interaction would be anticipated. First, for requestors within the business who are looking for resources to fulfill a need. These can come from Project Managers, the Proposal Group, Clinical Trial Managers, among others. The Second area is from Line Managers who have the resources to fulfill those requests. Communication with Line Managers about their Weekly Allocation uploads as required when errors or issues develop during the process.

    Summary of Responsibilities:

    • [20%] Manage the Resource Management Mailbox that is the centralized conduit for Resource Requests within CDCS. The purpose of this task is to read, interpret, and ensure appropriate emails are routed to the people who can fulfill the requests.
    • [20%] Manage and execute the weekly Allocation Upload Process. By close of business on Friday, 50-75 Excel Spreadsheets need to be uploaded into the Resource Management Tool via a Macro Tool developed by Resource Management.
    • [30%] Publishing of weekly reports from the Resource Management Tool. Each Week excel files are published to SharePoint from the Resource Management tool. Those Spreadsheets are generated via a Macro and do require mild manipulation prior to being published.
    • [20%] Base Line Resource Request (BRP) Loading into the Resource Management Tool. As work is awarded, an excel file from the Proposal/Contracting group is generated and needs to be loaded into the Resource Management Tool to populate the new Demand. Some Excel manipulation is required to ensure the proper format for an Excel Macro to run and perform the load.
    • [10%] Requires an understanding of the process and tools and has the ability to influence some change and enhancements to the process. Partnering with Manager develop different ways to streamline efficiencies and continuous improvement of process and tools.
    • All other duties as needed or assigned.

    Qualifications (Minimum Required):

    • University / college agree, or certification in related healthcare or resource management profession from an appropriately accredited institution
    • In lieu of the above requirement, candidates with four (5) or more years of relevant clinical research or resource management experience in pharmaceutical or CRO industry may be considered
    • Good understanding of the clinical trial process

    Experience (Minimum Required):

    • Minimum of three (5) years of professional experience.
    • In lieu of above requirement, candidates with four (4) years of clinical research (pharmaceutical research or contract research organizations) may be considered.
    • Strong ability to work within a project team.
    • Strong planning, organization, and problem-solving ability.
    • Strong oral and written communication and interpersonal skills.
    • Ability to work to deadlines and effective time management.
    • Ability to work with all levels of personnel.
    • Good analytical and problem-solving skills.
    • Good understanding of resource supply / demand principles.
    • Works efficiently and effectively in a matrix environment.
    • Excellent computer system and database knowledge and advanced MS Excel skills.
    • This position requires a higher level of process understanding and is the next level of the Coordinator Role I.

    Physical Demands/Work Environment:

    • Overtime and weekend work as required
    • Standard Office environment

    Learn more about our EEO & Accommodations request here.

    Skills Required

    • University or college degree, or certification in a related healthcare or resource management profession from an accredited institution
    • Four or more years of relevant clinical research or resource management experience in the pharmaceutical or CRO industry may substitute for the education requirement
    • Good understanding of the clinical trial process
    • At least three years of professional experience
    • Four years of clinical research experience in pharmaceutical research or contract research organizations may substitute for the professional experience requirement
    • Strong project team collaboration skills
    • Strong planning, organization, and problem-solving abilities
    • Strong oral, written communication, and interpersonal skills
    • Ability to meet deadlines and manage time effectively
    • Ability to work with personnel at all levels
    • Good analytical and problem-solving skills
    • Good understanding of resource supply and demand principles
    • Ability to work efficiently in a matrix environment
    • Excellent computer system and database knowledge
    • Advanced Microsoft Excel skills
    • Ability to work overtime and weekends as needed
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    The Company
    HQ: Durham, NC
    10,811 Employees

    What We Do

    Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.

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