Clinical Operations Excellence Lead Project Management FSP FSP
Clinical Operations Excellence Lead Project Management FSP FSP
Posted on :
14-02-2025
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1 Vacancy
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Monthly Salary
Not Disclosed
Salary Not Disclosed
Vacancy
1 Vacancy
Posted on :
14-02-2025
Job Description
Job Title: Clinical Operations Excellence Lead Project Management FSP FSP
Job Location: North Carolina USA
Job Location Type: Remote
Job Contract Type: Fulltime
Job Seniority Level:
Work Schedule
Standard (MonFri)
Environmental Conditions
Office
Clinical Operations Excellence Lead(COEL) Project Management FSP Dedicated
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 lifechanging 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.
Discover Impactful Work:
We are seeking a Global Clinical Operations Excellence Lead within our FSP Project Management Team.
The Clinical Operations Excellence Lead is responsible for the operational implementation of managing the quality of research & studies. This position is supporting our FSP Project Management team. This candidate would have experience from a: Project Management or Clinical Trial Management position with the focus in operational compliance. In addition this person must have experience supporting Clinical Operations functions. Examples: Quality Metrics Quality Systems process improvements inspection readiness etc. The successful candidate will excel in leadership and establishing good and effective internal and external working relationships and communication.
Role Details:
Thermo Fisher Scientific 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:
Standard (MonFri)
Environmental Conditions
Office
Clinical Operations Excellence Lead(COEL) Project Management FSP Dedicated
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 lifechanging 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.
Discover Impactful Work:
We are seeking a Global Clinical Operations Excellence Lead within our FSP Project Management Team.
- This role will be hired at Senior (level depending on experience).
The Clinical Operations Excellence Lead is responsible for the operational implementation of managing the quality of research & studies. This position is supporting our FSP Project Management team. This candidate would have experience from a: Project Management or Clinical Trial Management position with the focus in operational compliance. In addition this person must have experience supporting Clinical Operations functions. Examples: Quality Metrics Quality Systems process improvements inspection readiness etc. The successful candidate will excel in leadership and establishing good and effective internal and external working relationships and communication.
Role Details:
- Serves as the primary contact and lead between the sponsor and the organization at the project level.
- Responsible for oversight & ensures standards are met Global Clinical Operations.
- Responsible for commitments are met to regulatory requirements & reflected correctly in all necessary documents.
- Ensure quality risk management principles are integrated in all Global Clinical Operations processes and systems in order to support compliance and ensure inspection readiness throughout
- This candidate must be able to work cross functionally ensure alignment within other business units within the organization
- This candidate is responsible for driving investigations CAPA plans audits inspection findings etc.
- Drives and owns the overall delivery of the crossfunctional project (time cost quality).
- Establishes communicates and manages customer expectations to achieve optimal delivery during the project.
- Drives Risk Identification and Issue Resolution
- Ensures project team compliance with organization policies SOPs ICH GCP regulatory and project specific requirements.
- Bachelor's degree or equivalent and relevant formal academic / vocational qualification
- Advanced degree (Master or PhD) in healthrelated discipline or equal by experience is preferred
- Bachelor’s degree or University degree – medical or paramedical (Biology Biomedical Sciences Pharmacy Veterinary etc.) or equivalent by experience
- Minimum of 10 years of experience in Clinical and/or Pharmacovigilance Quality Management
- Working knowledge of the relationship and regulatory obligations of pharmaceutical/biotech companies and CROs
- Global Strategic Drug Development experience
- Years of experience refers to typical years of related experience needed to gain the required knowledge skills and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions.
- Extensive experience of GCP/Pharmacovigilance quality management systems applicable regulatory rules and guidelines medical terminology clinical trials and drug development
- Excellent interpersonal negotiation and leadership skills
- Strong written and verbal communication skills acting globally in a culturallydiverse dynamic team
- Ability to act independently and effectively prioritize
- Root Cause Analysis CAPA Development and Risk Management methodology expertise
- Clinical development guidelines and directives and regulatory guidelines
- Expert knowledge of the key principles of cross functional project management (Time Quality Cost).
- Excellent oral and written communication and presentation skills.
- Demonstrated leadership and interpersonal skills including the ability to lead motivate and coordinate crossfunctional project teams.
- Technical and systems competency such as computer skills to include effective use of systems and applications such as Microsoft Outlook Word Excel and PowerPoint as well as organization systems (CTMS Preclarus Clarity).
- Proven flexibility and ability to effectively prioritize workload and resources for project team members in a frequently changing environment.
- Skilled in process improvement and strategic development especially as it applies to clinical trials clinical development and project management.
- Ability to coach mentor and lead global and/or crossfunctional teams with a cultural awareness.
- Strong financial acumen with an indepth of knowledge and practical application of budgeting forecasting and resource management.
- Excellent consultation and relationship building skills.
- Excellent judgment decision making and problemsolving skills and proven ability to apply critical and analytical strategic thinking skills to manage complex/ambiguous situations.
- Proactive solutions oriented and skilled at risk identification and management.
Thermo Fisher Scientific 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.
- Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.
- May require travel. (Recruiter will provide more details.)
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Employment Type
Full Time
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