Associate Project Manager - Middleton, United States - Thermo Fisher Scientific

Thermo Fisher Scientific

Verified Company

Middleton, United States

2 weeks ago

Posted by:

Mark Lane

beBee recruiter

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.

Location/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:
Associate Project Manager - Labs

Department:
Clinical Research Group/ GMP Labs

Location:
Remote (United States)

Discover Impactful Work:

Liaises with PPD's operational divisions, affiliates and sponsors. Coordinates the study setup, maintenance and closure activities for identified protocols and/or study programs. Consults on project management issues and supports overall function of the Project Management group.

A day in the Life:

Serves as local study coverage for global studies and point of contact for clinical teams. Ensures timely completion of study activities and deliverables. Documents communication and actions with sponsors or with investigator sites.
Manages existing Batch, Supply only, & "In Conduct" studies. Develops new study setups as appropriate in collaboration with Tech Ops group.
Serves as designated backup for PM staff (Centralized) and point of contact

coverage for Project Managers when out-of office. Reviews and prepares with Project Managers in advance of coverage.

Advises project managers on procedural and budgetary items and the necessity for change due to any subsequent study modifications and/or protocol amendments. Monitors monthly Budget to Burn reviews and contract modifications.
Supports Project Management group with development and implementation of initial study supply orders to include: Creation of initial supply template, and submission of initial shipment requests to Supply Chain Management group.
Monitors completion of shipment requests.
Schedules group meetings and teleconferences (internal & external), prepares and distributes agenda, records and distributes minutes as required.
Monitors assignments and adjusts priorities and work schedule to meet deadlines and provide high quality deliverables. Completes additional tasks needed in support of project, client and departmental objectives.

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 02 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 selection decisions.
Preferred: Experience within project management and/ or central labs

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
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 uprigh