Senior/Principal Clinical Team Manager - Neuroscience at Thermo Fisher Scientific
Werk van thuis, , Netherlands -
Full Time


Start Date

Immediate

Expiry Date

13 Nov, 25

Salary

0.0

Posted On

14 Aug, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Presentation Skills, Neuroscience, Defense, Clinical Research, Ophthalmology, Thinking Skills, Ctm, Leadership, Ownership, Preparation, Psychiatry

Industry

Pharmaceuticals

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.
Our Project Delivery team advises, coordinates and leads the technical and operational aspects of projects, securing the successful completion of clinical trials. The team is therapeutically aligned to respond better to our customer needs.

WE ALSO SEE CANDIDATES WITH EXPERIENCE IN: BASKET, MASTER PROTOCOL AND ADAPTIVE TRIAL EXPERIENCE.

Currently, we are looking for an expert Clinical Team Manager to join our team. This exciting and unique role could take you the next step of your career within Clinical Research. As a Senior Clinical Team Manager (CTM), you combine deep knowledge, therapeutic expertise, and robust tools to help our clients deliver life-changing therapies to market. You take ownership, anticipate problems, find solutions and deliver results

The role coordinates all aspects of clinical activities on an international basis, including:

  • Day to day management and leadership of a team of Clinical Operations members who are allocated to a project on a Country basis
  • Responsibility for the achievement of the project clinical deliverables within the contractual timelines and budget
  • Development of clinical tools (e.g. Monitoring Plan and Guidelines) and set up of the required training, tracking and quality systems
  • Work in partnership with the Project Manager to prepare, organize, and present at client meetings, including bid defense and kick off meetings
  • Clinical Resource Management – provide input into preparation of forecast estimates of clinical deliverables, assignments and identification of additional resource requirements
  • Acting as a contact and support to the Sponsor for all clinical-related aspects of the project

KNOWLEDGE, SKILLS AND ABILITIES:

  • Outstanding organizational skills
  • Critical thinking skills
  • Proven performance management abilities
  • Excellent judgment and decision-making skills
  • Highly effective verbal and written communication and presentation skills
  • Experienced knowledge of relevant regulations e.g. ICH/GCP, FDA guidelines, etc.
  • Experience in Rare Diseases/ALS/Ophthalmology or Psychiatry

How To Apply:

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Responsibilities
  • Day to day management and leadership of a team of Clinical Operations members who are allocated to a project on a Country basis
  • Responsibility for the achievement of the project clinical deliverables within the contractual timelines and budget
  • Development of clinical tools (e.g. Monitoring Plan and Guidelines) and set up of the required training, tracking and quality systems
  • Work in partnership with the Project Manager to prepare, organize, and present at client meetings, including bid defense and kick off meetings
  • Clinical Resource Management – provide input into preparation of forecast estimates of clinical deliverables, assignments and identification of additional resource requirements
  • Acting as a contact and support to the Sponsor for all clinical-related aspects of the projec
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