Clinical Project Manager, Dermatology, Home-Based, Mexico, IQVIA Biotech page is loaded Clinical Project Manager, Dermatology, Home-Based, Mexico, IQVIA Biotech Apply locations Mexico City, Mexico time type Full time posted on Posted 5 Days Ago job requisition id R1365752 IQVIA Biotech is seeking a Clinical Project Manager to join our Dermatology Team. Qualified candidates will have several years of previous Project Management experience in a CRO or Sponsor environment.
PLEASE SUBMIT RESUMES IN ENGLISH.
BASIC FUNCTIONS:
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 and procedures set forth by IQVIA Biotech and sponsors. Supports the department director in... development of functional training, definition of standards and execution of department goals including process improvement.
ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES:
Responsible for all activities related to implementation of clinical studies including:
Manages projects of full scope regional and global projects. Responsible for project team leadership
Responsible for building and maintaining positive client relationships
Ability to negotiate with clients to assure IQVIA Biotech's operational processes are maintained, 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
Identifying, define, document training requirements in LMS systems and assure project level compliance with study specific training requirements
Responsible for change management on all assigned projects
Responsible for assuring projects assigned are run according to SOPs and WP as refined in the contract
Responsible for assuring project timelines are met as per contract
Responsible for identifying processes which need 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 In 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.
Provide other project support to Managers, as assigned
Oversee delegation of support staff activities, as necessary
Assists in the development and delivery of capability and proposal defense presentations to prospective clients
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 annually
Maintains 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

KNOWLEDGE, SKILLS AND ABILITIES:
Knowledge of clinical research process from Phase I through regulatory submission
Strong communication skills (verbal and written) to express complex ideas
Excellent organizational and interpersonal skills
Positive attitude and ability to interact with all levels of staff to coordinate and execute study activities
Ability to manage multiple priorities within various clinical trials
Ability to reason independently for the purpose of assessing and recommending specific solutions in clinical settings
Ability to set baseline targets, track trends and implement mitigation plans
Understanding of basic data processing functions, including electronic data capture
Working knowledge of current ICH GCP guidelines
CRITICAL 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 travel
Must be able to secure a credit card cosigned by IQVIA Biotech
MINIMUM RECRUITMENT STANDARDS :
Previous Management Requirements:
Nursing or University degree US Bachelor Level or equivalent) in a health-related field with a minimum of three (3) years direct clinical trial experience in a CRO or research-related organization with at least one (1) year management experience OR
Equivalent level of education and experience.
Previous experience in managing people within a scientific/clinical environment is preferred.
Clinical Monitoring or Data Management experience required.
Excellent and demonstrated verbal and written communication and presentation skills.
Ability to work independently, prioritize and work with in a matrix team environment is essential.
Working knowledge of Word, Excel, and PowerPoint required.
Prior experience in electronic data capture preferred.
Experience in contract/timeline management preferred
Excellent written and verbal communication skills required
Ability to travel domestically or internationally as required
CLASSIFICATION:
US: This position is classified as exempt under the Fair Labor Standards Act; employees are not eligible for overtime compensation.
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. 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. Learn more at https://jobs.iqvia.com
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