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Study Startup & Essential Documents Specialist

IUVO BIOSCIENCE OPERATIONS, LLC
Remote

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Job Details

$65,000 - $80,000 a year

Qualifications

Computer operation
Microsoft Excel
Microsoft Outlook
Computer literacy
Writing skills
Schedule management
Microsoft Teams
Standard operating procedures (SOPs)
Project stakeholder communication

Full Job Description

A Trusted CRO Partner for the Future of Eye Care

iuvo Clinical is a full-service ophthalmology-focused contract research organization (CRO) dedicated to improving patient’s quality of life with breakthrough eye care therapies. We combine decades of specialized experience with a high touch, high science approach, partnering with innovators to accelerate ophthalmic breakthroughs from concept to commercialization. Whether advancing a novel retinal therapy or supporting a complex ocular device trial, we provide the expertise, flexibility, and personal dedication to ensure your clinical trial’s success.

We offer a comprehensive benefits package and the opportunity to broaden your experience and grow your career!

We currently have an exciting opportunity for a Study Startup & Essential Documents Specialist.

SUMMARY

The Study Startup and Essential Documents Specialist (SSEDS) is responsible for supporting site start-up activities, including collection and review of essential documents for assigned investigative sites and Central IRB activities on a project and site-level. As a member of the Clinical organization, the SSEDS is responsible for assigned clinical programs and sites.

ESSENTIAL DUTIES AND RESPONSIBILITIES

Manage essential documents at a study-level from study start-up through close-out and at a site-level from site selection through close-out inclusive of IRB activities
Complete activities to confirm study and site-level eTMF completeness and document quality
- Set-up and maintenance of study-specific Regulatory Trackers as needed (in lieu of an electronic tracking system)
- Ongoing review of Regulatory Trackers (or electronic tracking system)
Responsible for Central IRB Management on a project and site-level
Complete Study-level IRB submissions inclusive of but not limited to:
- Assist with the development of Informed Consent Form and patient facing materials such as phone scripts, patient diaries, and advertisements as needed in preparation of study level IRB submission.
- Study-level close-out activities as applicable
Independently accountable for study start-up for assigned clinical sites
- Serve as the primary point of contact for assigned sites for start-up
- Assist sites with the completion of IRB applications and submissions
- Provide guidance and instruction on site completion of essential documents
- Send study start-up/required site activation documents to assigned clinical sites
- Organize, prepare, and ship applicable clinical study binders to clinical sites (regulatory binders, questionnaires, etc.) as needed
Collect and carefully review essential documents in accordance with Sponsor specifications
Responsible for Essential Document Quality, Completeness, and Processing
- Verify documents meet ALCOAC standards and are aligned with ICH/GCP and SOP requirements
- Follow study specific TMF Plan for classification of documents within the eTMF
- Collaborate with eTMF Administrator re: study-specific updates needed to the Veeva system as applicable
- Follow up with sites re: essential document action items through to resolution
Track site essential documents and maintain study trackers as assigned to provide real-time updates to Sponsor as requested
Primary point of contact for sites during the start-up process and essential document contact for the duration of the study (site activation forward)
Responsible for site-level essential document Action Item (AI) follow-up with sites (e.g., start-up/site activation documents, expired documents, missing documents, document updates) from the time of site-selection through site close-out
Collaborate with internal and external team members. Inclusive of but not limited to:
- Assist with eTMF follow-up required as a result of internal or external eTMF audits or site-level audit findings pertaining to the ISF
- Attend internal and external team calls to stay informed of current study status and provide feedback/updates as needed
- Develop collaborative relationships with investigative sites and internal and external team members. Review pertinent regulations to develop and communicate proactive solutions to start-up issues and challenges.
- Provide recommendations for improvement of project or divisional efficiencies based on work experience and observations
- Escalate site issues to applicable project team member
Other duties as assigned
Read and adhere to client-approved or iuvo SOPs

QUALIFICATIONS & REQUIREMENTS

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required.

EDUCATION and/or EXPERIENCE

Bachelor’s degree or equivalent job experience preferred
A clinical background with strong clinical site management/study start-up experience
Experience collecting, reviewing, and submitting regulatory documents and communicating with investigative sites is highly preferred
Experience in ophthalmology preferred.

COMPUTER SKILLS

Experience working with eTMF systems
Proficiency with Microsoft Office (Word, Excel, Outlook, Teams) and other software/programs as applicable to position

COMMUNICATION SKILLS

This position requires a person who communicates effectively both verbally and in writing with clinicians, clients, vendors, and internal project team members through demonstration of:

Excellent presentation and interpersonal skills, including clear, succinct, and timely communication
Sharing ideas in a constructive manner
Listening to and objectively considering ideas and suggestions from others
Keeping commitments
Keeping others informed of work progress, timetables and issues
Read and comprehend work instructions/SOPs and protocols and write clear, concise communications and documentation

OTHER SKILLS and ABILITIES

Highly organized
Must be able to efficiently schedule/perform follow-up of tasks, manage multiple priorities
Excellent time management
Attention to detail
Strong analytical skills

PHYSICAL DEMANDS

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.

While performing the duties of this job, the employee is regularly required to sit or stand at a desk, talk and hear.

WORK ENVIRONMENT

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Office setting / remote home office. iuvo Clinical fosters a video-first environment; employees are expected to have their cameras on for all internal and external meetings, check-ins, and collaborative sessions.

Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

LOCATION Remote

TRAVEL As required, estimated as <5%.

DISCLAIMER

This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities, and activities may change, or new ones may be assigned at any time with or without notice.

iuvo Clinical is an Equal Opportunity Employer

Quick Apply

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application development specialist jobs

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