Clinical trial manager Work, Jobs in Quebec, Dur (with Salaries)

Project Manager, CMC
Iksuda Therapeutics —Newcastle upon Tyne
- £42,000 - £48,000 a year
- Full-time
- Hybrid work
- Master's degree
- Project management
- Presentation skills
- Health & wellbeing programme
- Work from home
Quick apply
12d
Applied Psychologist (trial manager)
Tees, Esk and Wear Valleys NHS Trust —Sherburn ED
- £49,387 - £56,515 a year
- Part-time
- Doctoral degree
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Commercial Assistant
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Mental Health Support Worker
Changing Futures North East —Hartlepool
- £27,485 a year
- Full-time
- Applied behaviour analysis
- Working with children
- Psychology
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Project Manager, CMC

Iksuda Therapeutics
Newcastle upon Tyne

Quick apply

Job details

Permanent | Full-time
£42,000 - £48,000 a year
12 days ago

Benefits

Health & wellbeing programme
Free flu jabs
Company pension
Work from home
Company events
Flexible schedule
Life insurance
Sick pay

Qualifications

Biology
Programme management
Master's degree
Project management
Presentation skills
Bachelor's degree
Organisational skills
Contracts
Microsoft Project

Full job description

Iksuda Therapeutics is a Biotechnology Company focused on the development of Antibody Drug Conjugates (ADCs) for the treatment of cancer.

An exciting opportunity to join our team as a Project Manager, CMC is now available. The CMC Project Manager is responsible for cross-functional alignment of CMC activities leading to clinical development of antibody-drug conjugates targeting oncology indications. This individual will work closely with senior management and technical leads to create project plans, track progress against key milestones and integrate projects within the program portfolio.

Essential Functions and Duties:

Management of external vendors and coordination with the internal subject matter experts to ensure documentation and related activities are completed on time
Tracking and managing invoicing from external vendors ensuring they are aligned with pre-agreed proposals or agreements
Tracking and management of key inventories both internally and external vendor inventory
Manage the supply chain of key materials to facilitate manufacturing campaigns
Building and maintaining complex project plans
Ensuring effective and timely communication to team members and senior management regarding project status, key milestones, achievement of external and internal commitments and resource allocation
Managing meetings including scheduling, agendas, minutes, and actions
Driving cross-functional alignment to facilitate decision-making
Identifying strategic or operational issues impacting plan execution and working with the team on risk mitigation
Facilitating effective relationships among key team members

Experience required
3 years of relevant experience in program management in pharmaceutical or biotechnology drug development specifically within the area of CMC.

Skills and competencies required

Essential

Excellent documentation skills
Extremely well-organized with the ability to manage a highly-detailed workflow in the context of a broad strategic perspective
Self-motivated with expertise in both planning and implementation
Enthusiasm for working in a dynamic environment with a sense of urgency and aggressive timelines
Able to communicate effectively at all levels with internal employees and external collaborators, and with the ability to work collaboratively as a member of cross-functional and global team
Proficiency in project management, resource planning, and organizational skills
Competency with project management tools such as Microsoft Project
Ability to independently prioritize according to the business needs and be accountable for program/project execution
Ability to coordinate with other groups to identify and mitigate CMC program risks
Ability to manage external relationships with key vendors and contract manufacturing partners
Excellent written and presentation skills

Desirable

Experience in advancing oncology drug candidate from preclinical through Phase 1 and 2 clinical trials would be preferred
Understanding of GMP manufacturing, bio-analytics, CMC, QC/QA, and Regulatory considerations

Qualifications required

Essential

BSc in chemistry, biology or equivalent

Desirable

MSc in chemistry, biology or equivalent
Project management qualifications such as APM, AXELOS etc

Schedule:

Monday to Friday - Flexible hours

Work Location:

This is a hybrid role, predominantly working remotely with the flexibility to attend site meetings at the Company’s UK office as appropriate with visits to the US facilities and vendor sites as required.

MUST have UK Right to Work.

Please include a cover letter with your application.

Pay: £42,000.00-£48,000.00 per year

Benefits:

Company events
Company pension
Free flu jabs
Health & wellbeing programme
Life insurance
Sick pay
Work from home

Work Location: Hybrid remote in Newcastle upon Tyne NE4 5BX

Quick apply

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clinical trial manager jobs in quebec, dur

Project Manager, CMC

Applied Psychologist (trial manager)

Commercial Assistant

Mental Health Support Worker

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