Talent.com
Associate Director - Project Management - FSP - Drug Development exp

Associate Director - Project Management - FSP - Drug Development exp

Thermo FisherOakland, CA, US
17 hours ago
Job type
  • Full-time
Job description

Job Opportunity At Thermo Fisher Scientific

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.

Joining within our PPD FSP functional area, allows you to join the renowned PPD CRO and still gain invaluable client dedicated experience.

May serve in a Project Lead role, Oversight Director role or People Manager role within the Project Delivery Organization. Serves as the Project Lead and primary sponsor contact. Accountable for the overall delivery of the project (quality, time, cost) on behalf of the organization. Establishes and communicates customer expectations to the project team with minimal direction. Ensures that escalation pathways are adhered to internally and externally. Leads the cross-functional project team to meet or exceed deliverables. Manages project(s) of increasing complexity (such as but not limited to : multi-service, multiregion / country, therapeutic complexity, financial scope). The Oversight Director is accountable for strategic indication or client-specific portfolio management within a Therapeutic Unit. Provides therapeutic expertise in project delivery execution, demonstrating the ability to react quickly and appropriately to escalations. Provokes critical thinking in the Project Lead related to delivery operations, financial negotiations and risk mitigations / issue management for a project. Contributes to overall strategy development for proposals and pre-proposal opportunities. The People Manager directs a team of Project Delivery direct reports of differing levels of experience and project roles within a Therapeutic Unit. Accountable for the career development and performance management of their team, providing coaching in both soft skills and technical skills as related to the use of organization systems, tools and processes. Adept at identifying and addressing training gaps, while maintaining employee motivation and trust. The people manager fosters the ability to collaborate and balance business need with career development opportunities.

A day in the Life :

  • Serves as the primary contact between the sponsor and the organization at the project level.
  • Lead cross-functional teams in the development, optimization, and execution of eCOA frameworks to ensure efficiency, compliance, and seamless trial execution.
  • Serve as the eCOA SME across the organization, providing expert guidance throughout the end-to-end (E2E) process to ensure best practices and regulatory compliance.
  • Ensures financial stewardship at a project level by demonstrating an intimate understanding of the contract, resource alignment to budget, management of Out of Scope activity, drive the Con Mod process / negotiations and team execution to timelines.
  • Establishes, communicates and manages customer expectations to achieve optimal delivery during the project.
  • Drives Risk Identification and Issue Resolution at project level (RBQM / RESOLVE).
  • Ensures project team compliance with organization policies, SOPs, ICH-GCP, regulatory and project specific requirements
  • Oversee third-party vendors for copyright, translations, and library services, ensuring compliance with licensing agreements and regulatory requirements.
  • Design and implement a comprehensive training program to enhance internal expertise on eCOA processes, compliance requirements, and industry best practices.
  • Ensure continuous regulatory inspection readiness, maintaining complete documentation (including eCOA training), audit trails, and compliance with global regulatory requirements (ICH-GCP, FDA, EMA, and industry guidelines).

Keys to Success :

  • Master's or Bachelor's degree in Life Sciences, or a related field, or equivalent experience.
  • At least 10 years of drug development experience in distinct phases of development, in different disease areas, with a broader view on drug development (pre-clinical / commercial / scientific background)
  • At least 5 years of Program Management experience in a Pharmaceutical or Biotech environment, preferably cross-cultural.
  • Knowledge, Skills, Abilities :

  • Explore understanding and experience of pre-clinical drug development activities and commercial activities
  • Translate strategic plans into operational plans, control timelines and finances
  • Explore natural leadership skills, leading without authority / influencing skills, ability to work within flat organization / at ease with C-suite
  • Strong analytical skills and attention to detail to identify and resolve issues proactively.
  • Ability to work independently and cross-functionally, leading complex initiatives with minimal oversight.
  • Excellent communication, stakeholder management, and interpersonal skills.
  • Fluent in English (written and spoken).
  • PPD 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 for typical working hours.
  • Ability to use and learn standard office equipment and technology with proficiency.
  • May have exposure to potentially hazardous elements typically found in healthcare or laboratory environments.
  • Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.
  • May require travel. (Recruiter will provide more details.)
  • 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.

    Apply today!

    Thermo Fisher Scientific is an EEO / Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

    Accessibility / Disability Access

    Job Seekers with a Disability : Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255

  • . Please include your contact information and specific details about your required accommodation to support you during the job application process.
  • This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.

    Create a job alert for this search

    Associate Director Project Management • Oakland, CA, US

    Related jobs
    • Promoted
    Associate Director, Regulatory Affairs (Remote)

    Associate Director, Regulatory Affairs (Remote)

    Jazz PharmaceuticalsPalo Alto, CA, US
    Remote
    Full-time
    If you are a current Jazz employee please apply via the Internal Career site.Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to \ntransform the lives of patients and...Show moreLast updated: 1 day ago
    • Promoted
    Associate Director, CMC Regulatory

    Associate Director, CMC Regulatory

    Revolution MedicinesRedwood City, CA, United States
    Full-time
    Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The company’s R&D pipeline com...Show moreLast updated: 30+ days ago
    • Promoted
    Senior DMPK Director

    Senior DMPK Director

    ExelixisAlameda, CA, United States
    Full-time
    The Senior DMPK Director has strong scientific, technical and leadership skills to develop and implement DMPK and modeling & simulation strategies to advance drug candidates from discovery to devel...Show moreLast updated: 30+ days ago
    • Promoted
    Director, Project Management – IEP & HEOR

    Director, Project Management – IEP & HEOR

    Revolution MedicinesSan Francisco, CA, United States
    Full-time
    Director, Project Management – IEP & HEOR.Director, Project Management – IEP & HEOR.Director, Project Management – IEP & HEOR. Be among the first 25 applicants.Director, Project Management – IEP & H...Show moreLast updated: 30+ days ago
    • Promoted
    • New!
    Associate Director, CMC Program Management

    Associate Director, CMC Program Management

    Ultragenyx PharmaceuticalSan Francisco, CA, US
    Full-time
    Associate Director, CMC Program Management.Ultragenyx is looking for an Associate Director, CMC Program Management, with a passion and creativity to develop great medicines for rare and ultra-rare ...Show moreLast updated: 17 hours ago
    • Promoted
    Associate Director, Program Management

    Associate Director, Program Management

    Klein Hersh InternationalSan Francisco, CA, United States
    Full-time
    Our client is seeking an Associate Director, Project Management to join the Project Management team responsible for advancing exciting drug candidates into the clinic to treat diseases with high un...Show moreLast updated: 30+ days ago
    • Promoted
    Associate Director Program Management

    Associate Director Program Management

    Avails Medical, Inc.Menlo Park, CA, US
    Full-time
    We are seeking a proven leader to join our team as an.Associate Director / Director of Program Management.In this role, you won’t just manage projects—you’ll lead multidisciplinary ...Show moreLast updated: 3 days ago
    • Promoted
    Associate Director - Project Management- Market Lead

    Associate Director - Project Management- Market Lead

    Turner & TownsendSan Francisco, CA, US
    Full-time
    Associate Director - Project Management - Market Lead.Founded in 1952 and formerly known as Heery International Inc.United States as part of Turner & Townsend. It specializes in project and program ...Show moreLast updated: 30+ days ago
    • Promoted
    Sr. Manager / Associate Director, Drug Product

    Sr. Manager / Associate Director, Drug Product

    BridgeBioSan Francisco, CA, United States
    Full-time
    Manager / Associate Director, Drug Product.When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement.In 2015, w...Show moreLast updated: 30+ days ago
    • Promoted
    Associate Director, Clinical Development

    Associate Director, Clinical Development

    Revolution MedicinesRedwood City, CA, US
    Full-time
    Associate Director, Clinical Development.Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addict...Show moreLast updated: 30+ days ago
    • Promoted
    Associate Director, Contract Optimization and Strategy Team (COST)

    Associate Director, Contract Optimization and Strategy Team (COST)

    Revolution MedicinesRedwood City, CA, US
    Full-time
    Cost - Vendor Associate Director.Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cance...Show moreLast updated: 30+ days ago
    • Promoted
    Associate Director Clinical Pharmacology – San Francisco Biotech

    Associate Director Clinical Pharmacology – San Francisco Biotech

    TANNER & ASSOC INCSan Francisco, CA, United States
    Full-time
    Associate Director Clinical Pharmacology – San Francisco Biotech.New Position : Associate Director Clinical Pharmacology – San Francisco Biotech. The Associate Director role will have a broad range o...Show moreLast updated: 30+ days ago
    • Promoted
    Associate Clinical Programming Director

    Associate Clinical Programming Director

    ExelixisAlameda, CA, United States
    Full-time
    As a member of the Digital Strategy, Analytics, and Programming Leadership Team, this role guides and influences the strategic direction and priorities of the function and partners closely with the...Show moreLast updated: 30+ days ago
    • Promoted
    Associate Clinical Pharmacology & Pharmacometrics Director

    Associate Clinical Pharmacology & Pharmacometrics Director

    ExelixisAlameda, CA, United States
    Full-time
    The Associate Clinical Pharmacology and Pharmacometrics Director has strong scientific, technical and leadership skills to contribute to development and implementation of clinical pharmacology and ...Show moreLast updated: 22 days ago
    • Promoted
    Director, Project Management IEP & HEOR

    Director, Project Management IEP & HEOR

    Revolution MedicinesRedwood City, CA, US
    Full-time
    Director, Project Management Integrated Evidence Planning (IEP) & Health Economics And Outcomes Research (HEOR).Revolution Medicines is a clinical-stage precision oncology company focused on develo...Show moreLast updated: 30+ days ago
    • Promoted
    Director / Senior Director, Clinical Project Management

    Director / Senior Director, Clinical Project Management

    Valid8 Financial, Inc.San Francisco, CA, United States
    Full-time
    Director / Senior Director, Clinical Project Management.TCG Labs-Soleil is looking for a Director / Senior Director of Project Management who will report to the Chief Medical Officer.This individual wi...Show moreLast updated: 9 days ago
    • Promoted
    Associate Director, Regulatory Operations

    Associate Director, Regulatory Operations

    Revolution MedicinesRedwood City, CA, US
    Full-time
    Associate Director, Regulatory Operations.Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addic...Show moreLast updated: 7 days ago
    • Promoted
    Associate Director, Regulatory Affairs - Oncology

    Associate Director, Regulatory Affairs - Oncology

    Gilead Sciences, Inc.Foster City, CA, United States
    Full-time
    Associate Director, Regulatory Affairs - Oncology.At Gilead, we’re creating a healthier world for all people.For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 an...Show moreLast updated: 30+ days ago