*“What if your work could help advance innovative medicines for patients with some of the world's most challenging diseases?*
*In this embedded PPD™ Functional Service Partnership (FSP) role, you'll contribute to a global biopharmaceutical organization committed to transforming scientific innovation into meaningful advances for patients. You'll work closely with the client’s clinical development teams, contributing to research across therapeutic areas such as oncology, respiratory diseases, obesity, eye health, cardiometabolic conditions, and other areas of significant unmet medical need. As a valued member of an integrated FSP clinical team, you'll build deep client and therapeutic expertise, collaborate with experienced colleagues, and take ownership of work that contributes to the development of potentially life-changing treatments. Bring your expertise, curiosity, and commitment to patients to an environment where meaningful science meets purposeful collaboration. Apply today!*
What You’ll Do:
Ensure clinical trial execution excellence, including planning, coordination, and delivery of complex regulatory tasks at Study level.
Enable seamless trial operations and stakeholder communication.
Ensure timely availability of materials, documentation, and trial information.
Manage and maintain clinical systems and tools, ensuring accurate reporting and data tracking at study level.
Oversee trial supplies, documentation, submissions, and operational parameters
Compile and track trial data for internal and external reporting at study level.
Work independently while collaborating closely with CTL, CTMs, and trial teams across regions.
Education and Experience Requirements:
o Secondary education in Business Administration or equivalent o Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 2 years).
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills and Abilities:
Ability to work in a team or independently as required
Excellent organizational skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectively
Excellent ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency
Demonstrated flexibility and adaptability to reprioritize workload and provide efficient support to meet changing project timelines
Demonstrated ability to attain and maintain a good working knowledge of applicable Country
Regulations, ICH Good Clinical Practices, and organization/Client SOPs and WPDs for all non clinical/clinical aspects of project implementation, execution, and closeout
Excellent English language and grammar skills and proficient local language skills as needed
Effective presentation skills
Excellent computer skills, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems
Ability to successfully complete the organizations clinical training program
Self-motivated, positive attitude and strong interpersonal skills
Ability to use problem-solving techniques applicable to constantly changing environment
Ability to provide constructive feedback and suggest improvements to department processes
Effective oral and written communication skills, with the ability to communicate effectively with medical personnel
Good negotiation skills
Basic medical/therapeutic area and medical terminology knowledge
Basic knowledge of local health systems
Excellent customer focus
Ability to work in a matrix environment
A proven relationship builder
An independent thinker
Ability to manage risk and perform risk escalation appropriately
Working Conditions and Environment:
Work is performed in an office/ laboratory/clinical/ and/or home office environment with exposure to electrical office equipment.
Occasional drives to site locations. Potential Occasional travel required.
Thank you for your interest as you consider starting a new career journey with us. As the world leader in serving science, our colleagues develop critical solutions through innovation—and build rewarding careers. Discover their extraordinary [stories](https://jobs.thermofisher.com/global/en/discover-our-stories) and connection to our Mission to enable our customers to make the world healthier, cleaner and safer. Their work is a story of purpose. What story will you tell?
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of more than $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Thermo Fisher Scientific is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, creed, religion, color, national or ethnic origin, citizenship, sex, sexual orientation, gender identity and expression, genetic information, veteran status, age or disability status.
Healthcare
Senior
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