(Home-based) - Senior Consultant, Medical and Scientific Solutions/Low Complexity Non-Interventional Studies (LCNIS)

Senior Consultant, Medical and Scientific Solutions/Low Complexity Non-Interventional Studies (LCNIS)

Home-Based - Anywhere in the US

Overview of the team:

IQVIA LCNIS is a fast-growing team focused on designing and delivering innovative studies that use a range of primary data collection research methodologies (panel surveys, direct-to-patient and direct-to-physician surveys, chart review studies, site-based recruitment approaches), while following a light-touch, agile delivery approach.

Role Summary:

As a Senior Consultant within LCNIS, you will have the opportunity to develop and deliver observational studies using an array of research methods. The Senior Consultant is responsible for overall project management to ensure on-time and on-budget study delivery. Management includes oversight of activities within the internal team, as well as collaboration with other functional teams within IQVIA and external sub-contractors.

Responsibilities:

oSupports the delivery of custom primary data collection studies from initiation to completion, working independently but with oversight from a Director or Principal

oLeads client-facing activities; serves as primary point of contact for day to day study operations.

oLeads development, implementation and maintenance of operational strategy and planning.

oManages and follows study activities through ongoing tracking and review of study progress.

oAuthors protocols, surveys, case report forms, and reports in collaboration with the Principal and other study team members.

oLeads development and submission of documents for Institutional Review Board (IRB) review, including development of informed consent forms and other patient or site-facing materials.

oCollaborates internally with other functional groups, such as data generation, data management, quality assurance and biostatistics where necessary to support milestone achievement and to manage study issues and obstacles.

oOversees site management activities to ensure efficient and effective delivery of site management operations; may include assisting with site contract/budget review and reviewing and approving site visit reports.

oDevelops and delivers team training.

oContributes to business development for LCNIS, including developing proposals in response to RFPs and attending bid defense meetings.

oServes as a solutions-based expert, internally and externally, by applying consultative problem-solving skills.

oMay be assigned additional responsibilities as needed to support projects and other corporate/departmental initiatives.

Requirements:

oBA/BS required; MA/MS/MPH preferred

o4 or more years’ experience of related experience in clinical research, observational research, or other health-services research.

oKnowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP), Good Pharmacoepidemiology Practices (GPP), and International Conference on Harmonization (ICH) guidelines.

oDemonstrable competence in project management with proven time management and personal organizational skills.

oAble to manage complex relationships, juggle priorities, think critically and problem-solve

oDemonstrated team leadership and mentoring skills

oComputer skills including proficiency in use of Microsoft Word, Excel and PowerPoint

oStrong written and verbal communication skills

oAbility to manage competing priorities and ensure on-time, high quality delivery of project tasks/responsibilities.

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 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.

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 IQVIA’s Talent Acquisition team at workday_recruiting@iqvia.com to arrange for such an accommodation.