Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
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.
Division Specific Information:
Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought leaders and therapeutic experts. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations.
Title: Labs Project Manager I
Dept.: Lab Operations/ Global Central Labs
Location: Highland Heights, KY - Office based
Summarized Purpose:
Join Thermo Fisher Scientific Inc. as a Labs Project Manager I and manage projects, collaborate with professionals, and implement innovative solutions to improve processes within the Global Central Lab! This position will be work onsite at the Lab in Highland Heights, KY.
A day in the life:
Provide oversight and coordination of project initiation, ensuring seamless project start-up.
Review, interpret, translate, and program study protocols into a complete and accurate database.
Communicate with internal departments and external vendors to ensure project requirements are clearly understood, agreed upon, and followed.
Ensure smooth communication of technical and clinical laboratory information to collaborators, including investigational sites, sponsors, and non-technical personnel.
Consult with laboratory management and technical staff to assist clients in managing clinical trials.
Prepare study specifications documents, maintaining accurate version controls for specs, budgets, and contracts.
Ensure compliance with FDA and Good Clinical Practice guidelines, company SOPs, and other relevant regulations.
Educate investigator sites by delivering protocol-specific lab procedures presentations.
Collaborate with IT and data management teams to design, validate, and implement new software and functionalities.
Mentor and train junior personnel, identifying areas for development and efficiency improvements.
Education
Bachelor's degree or equivalent and relevant formal academic / vocational qualification
Experience
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years') or equivalent combination of education, training, & experience.
Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment election decisions.
Knowledge, Skills, Abilities
Good organizational skills with the ability to adapt and adjust to changing priorities and to manage multiple assignments with challenging/conflicting deadlines
Effective project management and organizational skills
Good computer skills
General knowledge of clinical trial processes and programs
Strong attention to detail and problem solving skills
Good written and verbal communication skills
Ability to effectively conduct oral presentations
Demonstrated experience in identification and resolution of technical problems in a professional environment
Ability to maintain a high degree of confidentiality with clinical teams
Ability to attain, maintain and apply a working knowledge of applicable procedural documents
Demonstrated positive attitude, enthusiasm toward work, and the ability to work well with others
Work Environment
Thermo Fisher Scientific 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 and/or standing for typical working hours.
Able to lift and move objects of 15 to 40 pounds
Able to work in non-traditional work environments.
Able to use and learn standard office equipment and technology with proficiency.
May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.
Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.
Exposure to fluctuating and/or extreme temperatures on rare occasions
Benefits
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
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.
