Job Description

Assoc Clin Project Mgr



Primary Location: Overland Park, Kansas, United States Full time R1173279 Date Posted: 12/29/2020

Job description

PURPOSE

Assist in the execution of the assigned regionally-based clinical study(ies) per Contract, from initiation through to closeout. Support all clinical study related activities for assigned projects in accordance with SOPs, policies and practices, meeting quality and timeline metrics.

RESPONSIBILITIES

Create, track and report on project timelines.

Produce and distribute status, tracking and financial reports for internal and external team members and senior management.

Assist the clinical project manager(s) with budget allocation and approval of invoices.

Serve as primary back up project contact with Sponsor and internal project team to ensure communication is maintained and reporting schedules are adhered to.

Identify out of scope project work. Escalate findings and action plans to appropriate parties.

Coordinate data gathering for the development of proposals for new work.

Prepare and present project information at internal and external meetings.

Coordinate with other project support staff within and outside the Clinical Project Management Unit to identify and consolidate support processes.

Undertake clinical project management activities as directed by Clinical Project Manager.

Train and may coordinate the work of more junior project support staff.

May provide direct site support (on site visits)

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

Understanding of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines

Basic therapeutic and protocol knowledge

Strong communication and interpersonal skills, including good command of English language

Good problem solving skills

Demonstrated ability to deliver results to the appropriate quality and timeline metrics

Good teamwork skills

Excellent customer service skills

Ability to work under limited direction

Strong software and computer skills, including MS Office applications

Ability to establish and maintain effective working relationships with coworkers, managers and clients

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

Bachelor's degree in life sciences or related field and 3 years clinical research experience; or equivalent combination of education, training and experience.

PHYSICAL REQUIREMENTS

Extensive use of keyboard requiring repetitive motion of fingers.

Extensive use of telephone and face-to-face communication requiring accurate perception of speech.

Regular sitting for extended periods of time.

May require occasional travel.

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.

IQVIA is an EEO Employer - Minorities/Females/Protected Veterans/Disabled

IQVIA, Inc. provides reasonable accommodations for applicants with disabilities. Applicants who require reasonable accommodation to submit an application for employment or otherwise participate in the application process should contact IQVIAs Talent Acquisition team at workday_recruiting@iqvia.com to arrange for such an accommodation.