Clinical Supplies Oversight Associate Director

1 semana atrás


São Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

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 Clinical Supplies Associate Oversight Director acts as liaison with internal and external stakeholders in the provision and marketing of department services. Builds and maintains client relationships. Collaborates with senior leadership and executive staff on strategic planning and business development. Oversees department project and process improvement strategy utilizing metrics and key performance indicators to manage performance and end results. Ensures compliance with established policies, procedures and regulations.

Essential Functions

  • Accountable for functional management of teams to ensure succesful execution of all department deliverables within assigned projects.
  • Responsible for liaising externally with clients and internally with other departments. Provides troubleshooting and advice on issues as needed.
  • Ensures that the department maintains accurate and timely processing of crossborder materials movement.
  • Assists senior management with business development efforts to ensure the securing of new business by making presentations to sponsors, developing and reviewing bids and proposals, and conducting contract negotiations through to closure with the sponsor.
  • Participates in global and/or cross-functional initiatives and improvement projects.
  • Contributes to the hiring, development and implementation of global, regional and local functions and plans.
  • Ensures staff is trained according to company policies and procedures.

Job Complexity:

Works on significant and unique issues where analysis of situations or data requires an evaluation of intangibles.

Job Knowledge:

Having broad expertise or unique knowledge, uses skills to contribute to development of company objectives and principles and to achieve goals in creative and effective ways.

Supervision Received:

Acts independently to determine methods and procedures on new or special assignments. May supervise the activities of others. Exercises independent judgment in methods, techniques and evaluation criteria for obtaining results.

Business Relationships:

Serves as consultant and spokesperson for the functional area on highly significant matters relating to operations, scheduling or specific phases of project or contracts. Creates formal networks involving coordination among groups.

Qualifications:

Education and Experience:

  • Bachelor's degree or equivalent and relevant formal academic / vocational qualification
  • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 10+ 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:

  • Excellent communication skills both written and verbal, including strong command of the English language
  • Excellent interpersonal, negotiation and problem solving/decisionmaking skills
  • Proven leadership and team building skills
  • Strong computer skills including Microsoft Office suite
  • In-depth understanding of clinical supplies operations, legislations and best practices
  • Excellent organizational and multi-tasking skills
  • Capable of designing, presenting, and implementing specific plans to deliver high quality products and services and to ensure that all tasks meet defined deliverables
  • Ability to work under pressure
  • Ability to motivate and integrate teams and teach/mentor team members

Management Role: No management responsibility

Working Conditions and Environment:

  • Work may be performed in a production, office or home-based environment with exposure to electrical office equipment.
  • Frequent travels both domestic and international

Physical Requirements:

  • Frequently stationary for 6-8 hours per day.
  • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
  • Moderate mobility required.
  • Occasional crouching, stooping, bending and twisting of upper body and neck.
  • Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
  • Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
  • Ability to communicate complex information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.
  • Frequently interacts with others, relates sensitive information to diverse groups both internally & externally.
  • Ability to apply abstract principles to solve complex conceptual issues. Requires multiple periods of intense concentration.
  • Performs a wide range of complex tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task.
  • Regular and consistent attendance.

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.

#J-18808-Ljbffr

  • São Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

    **Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office 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...


  • São Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

    Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job DescriptionAt 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...

  • Clinical Project Manager

    1 semana atrás


    Sao Paulo, Brasil CTI Clinical Trial Services, Inc Tempo inteiro

    **Clinical Project Manager** **(Level Depends on Experience)** **Job Purpose/Summary**: Responsible for management and oversight of assigned clinical trials (Phase I through Phase IV) to ensure client’s goals of time, budget and quality performance are met. The Clinical Project Manager I is expected to require support and guidance from Directors and/or...

  • Clinical Associate

    7 meses atrás


    Sao Paulo, Brasil Icon plc Tempo inteiro

    Recognize, exemplify and adhere to ICON's values which center around our culture of accountability, integrity, partnership, collaboration and excellence in delivery. - As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and...


  • São Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

    Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAt 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...


  • Sao Paulo, Brasil CTI Clinical Trial Services, Inc Tempo inteiro

    **Clinical Project Assistant** **Job Purpose/Summary** Responsible for supporting management efforts of Clinical Project Managers and Directors, ensuring timelines, and quality standards are being achieved. **What You’ll Do** - Support Clinical Project Manager / Director in completing management activities; supports activities through all phases of a...


  • São Paulo, Brasil buscojobs Brasil Tempo inteiro

    The Director, LATAM Clinical Operations will provide strategic leadership of the Clinical Operations function in emerging geographic regions, ensuring the successful execution of clinical trials from initiation to completion. As part of the leadership team, you will collaborate closely with cross-functional departments, including project management,...

  • Proj Mgr Clin Supplies

    8 meses atrás


    Sao Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

    Provides complete oversight of supply chain for complex global clinical trials. Ensures project/study activities are in compliance with company and client requirements. Acts as a representative for the department on all assigned projects. - Develops study specific plans for each assigned project. - Meets with internal teams to coordinate efforts, provide...


  • São Paulo, SP, Brasil Thermo Fisher Scientific Tempo inteiro

    **Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Job Description**: **Senior Director, Project Management - Oversight (Infectious Diseases)** **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...


  • São Paulo, SP, Brasil BeiGene Tempo inteiro

    PLEASE SUBMIT ALL RESUMES/CV'S IN ENGLISH FOR CONSIDERATION Language Requirement: Fluent English and Portuguese. Spanish is a plus. Preferred Experience: Pharmaceutical/Biotech Industry, Hematology, Oncology General Description: - Supports the Regional Clinical Study Manager in regional study delivery and ensures that delegated components of clinical...


  • São Paulo, São Paulo, Brasil Fortrea Tempo inteiro

    Company OverviewFortrea is a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience. We provide pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas.We...


  • Sao Paulo, Brasil Fortrea Tempo inteiro

    The Ass CRM is accountable for execution and oversight of local operational clinical trial activities and has ownership, oversight and impact on local regulatory and financial compliance, at a country operations level at the client in compliance with ICH GCP and country regulations. The position has a significant impact on how a country can deliver...


  • Sao Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

    Supports supply chain for moderate complex global clinical trials. Ensures project/study activities are in compliance with company and client requirements. May act as a representative and project lead for the department on less complex projects. - Develops study specific plans for each assigned project. - Meets with internal teams to coordinate efforts,...

  • Proj Mgr Clin Supplies

    7 meses atrás


    Sao Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

    PPD’s mission is to improve health. It starts as an idea to find a cure. It becomes a life saved. All in-between, it’s you! We know that meaningful results not only require the right approach, but also the right people. We invite you to re-imagine health promoting protocols with us, working alongside our talented, bright and energetic teams. From...


  • Sao Paulo, Brasil Curebase Tempo inteiro

    **About the role**: Curebase is seeking a Clinical Quality Associate I who will thrive in a quickly scaling healthcare technology environment. Quality at Curebase is deeply cross-functional, and you will work with nearly every function at the company to conduct risk-based quality management (RBQM) surveillance of Clinical Operations activities at Curebase....


  • São Paulo, Brasil S&P Global, Inc. Tempo inteiro

    Associate Director, Relationship ManagerApply locations Sao Paulo, BR Mexico City, MX time type Full time posted on Posted 7 Days Ago job requisition id 309960About the Role:Grade Level (for internal use): 12The Role/The Team: As the Associate Director - Relationship Manager, you will join a diverse, inclusive, and professional Market Outreach team...


  • São Paulo, Brasil Kyndryl Tempo inteiro

    Associate Director, Field MarketingAssociate Director, Field MarketingApply remote type: Partially Remotelocations: Sao Paulo (KBR51645)WeWork Officetime type: Full timeposted on: Posted 3 Days Agojob requisition id: R-28884Who We AreAt Kyndryl, we design, build, manage and modernize the mission-critical technology systems that the world depends on every...

  • Director/senior Director

    1 semana atrás


    Sao Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

    Our team of colleagues in clinical research services are at the forefront of getting cures to market. We bring a high caliber of scientific and clinical expertise to the development of drugs that address the world’s most challenging health concerns. Our Clinical Research team, who powers our PPD® clinical research portfolio, are part of our leading global...


  • São Paulo, Brasil Thermo Fisher Scientific Tempo inteiro

    Job DescriptionSummarized Purpose:Supports supply chain for moderate complex global clinical trials. Ensures project/study activities are in compliance with company and client requirements. May act as a representative and project lead for the department on less complex projects.Essential Functions:Develops study specific plans for each assigned project.Meets...


  • Sao Paulo, Brasil IQVIA Tempo inteiro

    Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...