Job Description

RWE Assoc Site Mgmt Lead



Primary Location: Durham, North Carolina, United States Full time R1171210 Date Posted: 01/20/2021

Job description

Job Overview
Lead the execution of the Site & Patient Services (SPS) components of Real World Late Phase Research (RLWPR) studies by applying clinical research expertise, exceptional decision-making skills and innovative approaches to problem solving. Proactively set project goals and tangible expectations for SPS project team members.

Essential Functions
Oversee the delivery of Site Management project tasks, providing advice and guidance to achieve high performance and quality project deliverables.
Ensure overall project efficiency and adherence to project timelines and financial goals; report metrics and out of scope activities.
Develop, implement and maintain the Site Recruitment, SPS Operations and SPS Risk Management Plan within the agreed project strategy.
Collaborate with other functional groups within the company such as data management, quality assurance and biostatistics where necessary to support milestone achievement and to manage study issues and obstacles.
Manage and follow study activities through ongoing tracking and review of study progress. Provide input and report progress to appropriate SPS management and project management leaders.
Act as the first line of escalation for site management questions and issues on assigned projects.
Lead preparation for in-house audits and in creation of Corrective Action Plans (CAPAs).
Develop and deliver presentations/training to clients, colleagues and professional bodies, as required.
Participate in business development activities such as proposal development and bid defence.
May conduct co-monitoring and/or assessment visits as needed to ensure the study is being conducted in accordance with the protocol, SOPs, GCP and applicable regulatory requirements.
May be assigned additional responsibilities as needed to support projects and other corporate/departmental initiatives.

Qualifications

Life sciences educational background
Prior experience and knowledge of clinical operations monitoring processes, documentation, GCP standards
In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Skill in understanding and executing complex study designs.
Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint.
Strong written and verbal communication skills including good command of English language
Demonstrated team leadership and mentoring skills.
Demonstrated ability to develop and deliver project and functional training.
Excellent planning, organizational and problem-solving skills.
Ability to manage competing priorities and ensure on time, high quality delivery of project tasks/responsibilities.
Ability to establish and maintain effective working relationships with co-workers, managers and clients.

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.