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Associate Project Manager

extra holidays - extra parental leave
Remote: 
Full Remote
Work from: 

Offer summary

Qualifications:

Grade 12 or equivalent, Project Management experience beneficial, Coordinational experience advantageous, Intermediate Excel skills.

Key responsabilities:

  • Coordinate technical and service aspects of projects
  • Manage logistics for investigational medicinal products
Thermo Fisher Scientific logo
Thermo Fisher Scientific Biotech: Biology + Technology Large https://www.thermofisher.com
10001 Employees
HQ: Waltham
See more Thermo Fisher Scientific offers

Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Business Job Title: Associate Project Manager

About Thermo Fisher Scientific:

At Thermo Fisher Scientific, each one of our 90,000 extraordinary minds have a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner and safer.

When you’re part of Thermo Fisher Scientific, you’ll do challenging work, and be part of a team that values performance, quality and innovation. As part of a successful, growing global organization you will be encouraged to perform at your best.

Thermo Fisher Scientific provides industry leading pharma services solutions for drug development, clinical trial logistics and commercial manufacturing to customers of all sizes through our Patheon brand.

Location/Division:

Thermo Fisher Scientific, Clinical Trials Division, Centurion (Remote – Kenya), Gauteng, South Africa

Reports To: Project Manager South Africa

Position Objective:

You will be responsible to support our client’s clinical trials by managing the clinical study requirements from study setup, through to day-to-day activities and study close out. The holder of this position is independent in carrying out assigned tasks listed below and expected to practice continuous improvement and self-training on our quality management system.

What will you do?

  • Coordinating technical and service aspects of a given project, ensuring compliance with study requirements, ensure day to day operational study requirements are met
  • Managing logistics for importation and delivery of investigational medicinal products
  • Provide training to team members and stakeholders
  • Participating in internal and external meetings
  • Maintaining compliance with established procedures and standards
  • Contributing to corporate goals
  • Assisting in the investigation of non-conformances and customer complaints
  • Liaising with global project managers or clients on drug returns and destruction requirements
  • Timely provision of reports
  • Design, implementation, maintenance and reporting of key performance indicators
  • Continuous improvement and self-training on the quality management system
  • Maintain the quality adherence through all processes
  • Communication with clients and global project managers

How will you get here? Education

  • Grade 12 or equivalent
  • Project Management experience will be beneficial
  • Any co-ordinational experience will be an advantage
  • Excel intermediate level
  • Clinical trial industry experience will be an advantage

Knowledge, Skills, Abilities:

  • Effective time management and prioritization skills Self-driven and motivated
  • Ability to work independently and be self-motivated with a positive attitude
  • Collaborate cross departmental and cross organizational
  • Customer focused
  • Detailed orientated
  • Financially orientated
  • Ability to work under pressure and meet tight deadlines
  • Strong excel capabilities

Required profile

Experience

Industry :
Biotech: Biology + Technology
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Microsoft Excel
  • Motor Coordination
  • Self-Motivation
  • Calmness Under Pressure
  • Collaboration
  • Time Management
  • Detail Oriented

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