Study Vendor Specialist (BuyerPlanner)

Work Schedule

Environmental Conditions

Job Description

As part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer.

Join our team as a Buyer/Planner II where youll contribute to global healthcare and scientific this role youll optimize inventory management and vendor relationships while ensuring seamless supply chain operations. Working with cross-functional teams youll analyze demand requirements manage purchase orders and implement continuous improvement initiatives to support our mission of enabling customers to make the world healthier cleaner and safer.

This is a fully remote position for candidates located in the United States.

*Must be legally authorized to work in the United States withoutsponsorship.

*Must be able to pass a comprehensive background check whichincludes a drug screening.

Essential Functions:

• Manage third-party study vendors including study specification creation collection and finalization in conjunction with the relevant functional SMEs.
• Responsible for the day-to-day management and oversight of third-party vendors at the study-level.
• Responsible for keeping SMT updated regarding progress issuestracking
• Ensure study level contracted timelines and deliverables are clear and managed in the context of the vendor.
• Proactively identify elevate/escalate vendor issues that arise during study conduct to bring to resolution.
• Manage and measure performance of the vendor on assigned study
• Work with vendor to align KPI study delivery management and measurement of vendor performance escalating.
• Demonstrate appropriate oversight of vendors through regular well-structured meetings with vendors (including agendas and minutes)
• Work with Biogen FSP Oversight Manager Procurement to define project study specs and develop the Vendor Oversight Plan.
• SVS will drive development of specific study level vendor management plans
• Develops required study specific vendor materials
• Support the coordination of vendor performance management meetings to a study level.
• Provide accurate and up-to-date study level vendor information in relevant technology systems
• Driving the cross-functional collaboration and problem solving to ensure study level vendor risk identification and mitigation.
• Work closely with functional quality representatives (FQRs) to ensure vendors project deliverables meet quality standards.
• Ensures vendors compliance with relevant Biogen policies and procedures.
• Facilitate effective communication and collaboration between SMT and vendor.
• Ensures deliverable transparency from vendor to enable ease of invoice review and responsible for alerting Clinical Trial Lead CTL to invoice anomalies or inconsistencies

Minimum Requirements:

• High School diploma or equivalency (bachelors degree preferred)
• 2 years in clinical operations management managing clinical studies per quality timeline and budget expectations with a Sponsor company or a CRO.
• Exceptional project-management risk-assessment contingency-planning and communication skills and strong cross functional collaboration.
• Knowledge of clinical study management preferably related to one or more study phases (I II III)
• Strong understanding and practical application of Good Clinical Practices (GCP) International Council for Harmonization (ICH) guidelines and regulatory requirements for clinical development
• Demonstrated ability to establish and execute vendor plans according to study needs.
• Clinical Study Management experience working with third party vendors (preferred)

Salary Transparency:

This is a salaried role that will also be eligible to receive a variable annual bonus based on company team and/or individual performance results in accordance with company policy. Compensation will be initially discussed during the screening period with actual compensation confirmed in writing at the time of offer.

We offer a comprehensive Total Rewards package that our US colleagues and their families can count on which generally include:

A choice of national medical and dental plans and a national vision plan

A wellness program and valuable health incentive opportunities for company contributions to a Health Reimbursement Accounts (HSAs) or Health Savings Account (HSA)

Tax-advantaged savings and spending accounts and commuter benefits

Employee assistance programs

At least 120 hours paid time off (PTO). 10 paid holidays annually paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave) accident and life insurance short- and long-term disability and volunteer rime off in accordance with company policy.

Retirement and savings programs such as our competitive 401(k) U.S. retirement savings plan

Accessibility/Disability Access:

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.

EEO & Affirmative Action:

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.