(Senior) Project Manager - Global Clinical Supplies

at  Thermo Fisher Scientific

távmunka, , Hungary -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate18 Jan, 2025Not Specified19 Oct, 2024N/ACommunication Skills,Customer Service,Perspectives,Technological Innovation,Clinical Supplies,Research,Bid Preparation,Training,DefenseNoNo
Add to Wishlist Apply All Jobs
Required Visa Status:
CitizenGC
US CitizenStudent Visa
H1BCPT
OPTH4 Spouse of H1B
GC Green Card
Employment Type:
Full TimePart Time
PermanentIndependent - 1099
Contract – W2C2H Independent
C2H W2Contract – Corp 2 Corp
Contract to Hire – Corp 2 Corp

Description:

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.
We have a vacancy for Project Manager/Sr Project Manager to join our Global Clinical Supplies Team in the EMEA region. This can be office based, hybrid, or fully homebased in a number of EMEA locations (note that level will be decided after interview).

A DAY IN THE LIFE:

  • Develops study specific plans for each assigned project.
  • Meets with internal teams to coordinate efforts, provide recommendations and risks, and update project reports/spreadsheets.
  • Integrates all clinical supplies activities into the supply chain to support project logistic strategy and compliance with GxP requirements.
  • Participates in ongoing training on new regulations.
  • Represents the department internally and externally at meetings, strategic projects and initiatives as per the business requirements.
  • Mentors and guides supports junior team members.
  • Participates in process improvement initiatives.
  • Maintains and uses existing tools while continously looking for improvement opportunities
  • May participate in the bidding and/or bid defense opportunities
  • Client contact for their supply chain strategy/requests/questions/concerns Participates in ongoing training on new regulations

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 5 (PM) 8+ (SrPM) years). Preferably eith experience of clinical supplies in a clinical trial environment.
    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 English and communication skills both written and verbal
  • Excellent interpersonal, planning, organizational, problem solving, sense of urgency and decision making skills.
  • Demonstrated leadership and team building skills
  • Strong working knowledge of Microsoft Office suite
  • In-depth focus on customers and attention to detail
  • Ability to work in team environment, as well as work completely independent
  • Comprehensive understanding of clinical supply operation
  • Strong client building and 3rd party relationship management
  • Outstanding ability to provide customer service with the highest standards of quality and excellence
  • Skillful in bid preparation and bid defense
    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.
    Apply today! http://jobs.thermofisher.com

Responsibilities:

Manages full supply chain oversight for complex global clinical trials. Ensures project/study activities are in compliance with company and client requirements.. Acts as a department representative on all assigned projects and provides consultation services to clients.


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Proficient

1

távmunka, Hungary