Associate Clinical Project Management Director, Cardiovascular/Renal/Metabolic (Home-Based) - IQVIA

Employer
IQVIA
Location
Frederick, MD
Posted
Sep 18, 2020
Closes
Sep 22, 2020
Ref
1212550735
Industry
Other
Hours
Full Time
BASIC FUNCTIONS:Manages projects of full scope regional and global programs. Responsible for the successful planning, implementation and execution of contracted activities. Assures the accurate transfer of contracts from proposal through project completion. Functionally responsible for all team members throughout the duration of each clinical trial. Assures clear client communication, process documentation, and compliance with Good Clinical Practices (GCP) and procedures set forth by IQVIA Biotech and sponsors. Supports the department director in development of functional training, mentoring, and definition of standards and execution of department goals including process improvement.Supports the department director in development of functional training, mentoring, and definition of standards and execution of department goals including process improvement.Supports generation of new business opportunities including conducting early engagement activities, providing input to client proposals including and participating in bid defense. Provides support in client negotiations, internal process implementation, and trend analyses. ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES:Manages projects of full scope regional and global programs. Responsible for project team leadership. May operationally oversee the work of other project management staff.Responsible for building and maintaining positive client relationships and keeping all project reporting current and assuring executive management is aware of issues putting IQVIA Biotech at financial or regulatory risk through the approved upon pathways for reporting.Ability to negotiate with clients to assure IQVIA Biotech's operational processes are maintained and projects are done within scope.Reviewing and identifying project study trends and proactively responding to client and respective team members.Developing appropriate early warning systems of potential obstacles to the successful completion of the projects; analyzes information and develops innovative solutions to challenges.Identify, define, document in requirements in LMS systems and assure project level compliance with study specific training requirements.Responsible for change management on all assigned projects.Ability to independently resolve project related issues.Responsible for assuring projects assigned are run according to SOPs and WP as defined in the contract.Responsible for assuring project timelines are met as per contract.Responsible for identifying study processes which need to be created or updating and documenting that to the direct line manager or divisional lead.Responsible for maintaining client relationships for all assigned work, keeping all project reporting current, and assuring executive management is aware of issues putting IQVIA Biotech at financial or regulatory risk through the approved upon pathways for reportingIn conjunction with management, assists with developing, documenting, and updating internal processes and processes required for consistency across programs such as SOPs, working practices, and related quality assurance forms.Assists in communication of budget allocations and approval of invoices.Provide other project support to Managers, as assigned.Oversee delegation of support staff activities, as necessary.Provides required and supplemental training to staff. Provides ongoing feedback regarding staff performance and assesses performance at least annually with quarterly documented review of goals. Makes recommendations regarding salary adjustments.Assures compliance with Good Clinical Practices (GCP) within all Clinical Program Services (CPS) functional areas.Responsible for identifying processes which need updating and documenting that to the divisional lead.Leads the development and delivery of capability and proposal defense presentations to prospective clients. Takes a cross functional leadership role in assuring client presentations are effectiveAbility to present personal skills and IQVIA Biotech capabilities in any client presentation resulting in work awards.Supports Contracts and Proposals with final project contract execution and CIS documentation by the project team. Represents senior management in negotiation of contracts as appropriate.Participates in the performance appraisal program by providing timely and accurate feedback regarding the performance of respective team members at least annuallyMaintains current knowledge of FDA regulations, and GCP and ICH Guidelines for clinical research.Responsible to maintain personal currency documentation for IQVIA Biotech SOPs, CAPA completion and timesheet maintenance including assurance or back-up PM staff at every instance of out of office. In addition, responsible to assure currency for those within the Program Director's reporting linePerforms other duties as required.Authorized to:Negotiate deliverable timelines with clients leading to contract amendmentsNegotiate scope of work agreement with clients as per company policyApprove project direct and pass-thru expenditure as per company policyResponsible for all activities related to implementation of clinical studies, when responsible for project management, including:Project team leadershipCommunicating and documenting interactions with clients based on SOPsDefining and implementing functional standards, goals, and expectationsAssuring thorough planning and effective implementation of trials based on contracted scope of work, project timelines, and milestonesManaging ongoing team activityReviewing project budgets, monitoring costs, potential overruns and implementing cost effective solutionsReviewing and identifying project study trends and proactively responding to client and respective team members at least annuallyDeveloping appropriate early warning systems of impending obstacles to the successful completion of the project, analyzes information and develops innovative solutions to challengesKNOWLEDGE, SKILLS AND ABILITIES:Knowledge of clinical research processStrong communication skills (verbal and written) to express complex ideasExcellent organizational and interpersonal skillsPositive attitude and ability to interact with all levels of staff to coordinate and execute study activitiesAbility to manage multiple priorities within various clinical trialsAbility to reason independently for assessing and recommending specific solutions in clinical settingsAbility to set baseline targets, track trends and implement mitigation plansDemonstrated knowledge of electronic data management operationsDemonstrated knowledge of quality assurance related to clinical trial implementationDemonstrated ability to form strong working relationships across functional boundariesDemonstrated ability to motivate, and lead a project management teamDemonstrated financial and operational management, negotiation and problem-solving skills Extensive experience with monitoring and/or data management supervision according to Good Clinical PracticesExperience with pharmaceutical product development in a CRO environmentExcellent knowledge of FDA and/or ICH guidelines for conducting clinical researchExceptional ability to conceptualize, develop and manage process solutions and work with clients in all phases or research programsCRITICAL JOB FUNCTIONS IN ACCORDANCE WITH ADA CRITERIA:Very limited physical effort required to perform normal job duties.Up to 20% travel may be required including international travelMINIMUM RECRUITMENT STANDARDS: Previous Management Requirements:Nursing or University degree (US Bachelor level or equivalent) in a health-related field preferred with at least five (5) years of demonstrated clinical trial project management experience, ORMinimum two (2) year degree with equivalent experience, ORWithin the total years of experience, at least five (5) years clinical trial project management experience in a CRO-related position preferredWorking knowledge of all functional areas of clinical trials management (ie: Clinical, DM, Bios, Programming, MW, etc.)Clinical Monitoring or Data Management experience required. Excellent and demonstrated verbal and written communication and presentation skills. Excellent demonstrated knowledge of issues affecting data analysis for clinical trials is required. Ability to travel domestically and internationally as required.CLASSIFICATION:US: This position is classified as exempt under the Fair Labor Standards Act; employees are not eligible for overtime compensation.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/DisabledIQVIA, 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. Full time

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