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Study Start Up & Feasibility Specialist at GI Alliance – Cedar Park, Texas

GI Alliance
Cedar Park, Texas, 78613, United States
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Recently UpdatedIndustries:Healthcare / Health ServicesJob Function:Admin/Clerical/Secretarial

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About This Position

Study Start Up & Feasibility Specialist
Job DetailsJob Location: Urology Austin Cedar Park - Cedar Park, TX 78613
Position Type: Full Time
Job Shift: Day
Description

Description


Position purpose


The Study Start Up & Feasibility Specialist ensures rapid study start up and manages all aspects of the feasibility process across sites.


Responsibilities/Duties/Functions/Tasks:


• Manages client feasibility communications including site submission, completion of questionnaires, and other requests on behalf of assigned sites as directed


• Oversees the internal feasibility process ensuring essential data (EHR, CTMS) and key stakeholder feedback is incorporated


• Collaborates with legal and leadership to ensure the tracking, documentation, and signatures for all NDAs/CDAs are completed at the time of feasibility


• Ensures timely submission of, and follow up on, all feasibility questionnaires and site submissions to clients, while keeping CRM data updated and organized in real time


• Provides timely and thorough pipeline updates to clinic operations, regulatory, and contract teams at every stage of PSV, study awards and study start-up


• Attends PSVs to ensure continuity in prior communications, to capture study updates affecting feasibility, and to gather details and timelines related to study start up


• Drives PSV and study startup optimization via successful hand-off of study details and client communications to other departments. Leads PSV training efforts with clinical operations to close the sales cycle


• Owns all CRM data including upkeep of all internal research site information, current study updates, and new opportunity details in the study pipeline


• Provides scheduled and on-demand pipeline and departmental updates to leadership and local site teams


• Works alongside research leadership and Principal Investigators to determine study site selection


• Creates and maintains client facing presentations and marketing materials to showcase network capabilities


• Manages preparation, including any documentation needed, for any client meeting


• Maintains investigator CV addendums with updated clinical trial history


• Leads data entry process of business development activities in the CRM related to opportunity state progression through the entire study cycle


• Acts as the face of the network alongside physicians in various industry meetings


• Organizes, creates documentation for, and attends study kick off calls for all new studies entering study-startup


• Works with all shared service departments to drive rapid study start up. Supports client communications as requested after local site handoffs


• Is the central communicator between all shared service departments to ensure study start up tasks are on track and being completed on time


• Reports monthly start up metrics to leadership


• Maintains start up activities/communications within the CTMS system


• Supports other business development or start up functions as necessary



Qualifications

Qualifications


Qualifications


Education:


• Bachelor’s Degree from an accredited university preferred


Experience:


• Urology research experience preferred


• Minimum of 3 years of clinical research required


• Business development experience within the research industry preferred


Other Requirements: Travel within the United States may be required



Performance Requirements:



• Knowledge of grammar, spelling, and punctuation.


• Skill in operating office equipment.


• Skill in answering the phone and responding to questions.


• Skill in time management, prioritization, and multitasking.


• Skill in writing and communicating effectively.


• Ability to work under pressure, communicate and present information.


• Ability to read, interpret, and apply clinic policies and procedures.


• Ability to identify problems, recommend solutions, organize and analyze information.


• Ability to multi-task, establish priorities, and coordinate work activities.


• Ability to competently use Microsoft Office, including Word, PowerPoint, Excel, and appropriate practice management software.



Equipment Operated: Standard office equipment including computers, fax machines, copiers, printers, telephones, etc.



Work Environment: Position is remote with some travel to industry meeting and clinical research sites as needed.



Physical Requirements: Must possess the physical and mental abilities to perform tasks such as sitting for 90 percent of the day; manual dexterity to operate office machines including computer and calculator; stooping, bending to handle files and supplies; and mobility to complete errands or deliveries. Stress can be triggered by multiple staff demands and deadlines.

Job Location

Cedar Park, Texas, 78613, United States
Loading interactive map for Cedar Park, Texas, 78613, United States

Job Location

This job is located in the Cedar Park, Texas, 78613, United States region.

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