Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.
The PPD FSP Solution:
PPD's Functional Service Provider division partners with and serves as an extension of our PPD team, supporting our customers' key functions. We cover customer needs on every level, allowing them to do more with less, with an uncompromising commitment to quality. We deploy the same top-tier talent in ALL engagement models. Exceptionally trained, rigorously supported and technologically empowered to help customers manage capacity and set programs up for success.
Joining within our PPD FSP functional area allows you to join the renowned PPD CRO and still gain invaluable client dedicated experience.
Discover Impactful Work:
The AD, Project Management - eCOA serves as a functional subject matter expert (SME) in the field of electronic Clinical Outcome Assessments (eCOA), driving process optimization, standardization, and operational excellence across clinical programs. This role collaborates closely with many cross-functional departments to enhance efficiency and effectiveness in eCOA implementation.
By providing strategic oversight, governance, and continuous process improvements, the successful candidate will ensure that eCOA solutions are seamlessly integrated, fully compliant with regulatory requirements, and enhance the patient and site experience to ensure an optimal level of robustness for data captured via eCOA.
A day in the Life:
* Serves as the primary contact between the sponsor and the organization at the project level.
* Leads cross-functional teams in the development, optimization, and execution of eCOA frameworks to ensure efficiency, compliance, and seamless trial execution.
* Serves as the eCOA SME across the organization, providing expert guidance throughout the end-to-end (E2E) process to ensure best practices and regulatory compliance.
* Ensures financial stewardship at a project level by demonstrating an intimate understanding of the contract, resource alignment to budget, management of Out of Scope activity, driving the Con Mod process/negotiations and team execution to timelines.
* Establishes, communicates and manages customer expectations to achieve optimal delivery during the project.
* Drives Risk Identification and Issue Resolution at project level (RBQM/RESOLVE).
* Ensures project team compliance with organization policies, SOPs, ICH-GCP, regulatory and project specific requirements.
* Oversees third-party vendors for copyright, translations, and library services, ensuring compliance with licensing agreements and regulatory requirements.
* Designs and implements a comprehensive training program to enhance internal expertise on eCOA processes, compliance requirements, and industry best practices.
* Ensures continuous regulatory inspection readiness, maintaining complete documentation (including eCOA training), audit trails, and compliance with global regulatory requirements (ICH-GCP, FDA, EMA, and industry guidelines).
Keys to Success:
* Master’s or Bachelor’s degree in Life Sciences, or a related field, or equivalent experience.
* Minimum 8 years of experience in clinical trials within the pharmaceutical or biotechnology industry, with direct eCOA implementation responsibilities.
* Proven expertise in system implementation, vendor management, and process development of eCOA.
Knowledge, Skills, Abilities
* Expert knowledge of eCOA methodologies, regulatory guidelines (ICH-GCP, FDA, EMA), and industry best practices.
* Deep understanding of eCOA systems, technical implementation, and operational workflows.
* Strong analytical skills and attention to detail to identify and resolve issues proactively.
* Ability to work independently and cross-functionally, leading complex initiatives with minimal oversight.
* Excellent communication, stakeholder management, and interpersonal skills.
* Fluent in English (written and spoken).
PPD values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:
* Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
* Able to work upright and stationary for typical working hours.
* Ability to use and learn standard office equipment and technology with proficiency.
* May have exposure to potentially hazardous elements typically found in healthcare or laboratory environments.
* Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.
* May require travel. (Recruiter will provide more details.)
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Apply today! http://jobs.thermofisher.com
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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