Regulatory project manager Work, Jobs in Alsager, Chs (with Salaries)

Clinical Project Manager
Biocomposites —Keele
- Full-time
- Organisational skills
- Leadership
- Communication skills
- Free parking
- Employee discount
Quick apply
1d
Senior Project Manager
KION Group AG —Stockport
- Full-time
Client Services Manager
Wren Sterling —Wilmslow
- £45,000 - £52,000 a year
- CRM software
- Project management
- Continuous improvement
Quick apply
2d
Risk Management Specialist
Biocomposites —Keele
- Full-time
- Management
- Leadership
- Communication skills
- Free parking
- Employee discount
Quick apply
2d
Sustainability and Ethics Officer
Kingsland Drinks —Manchester
- £35,000 - £45,000 a year
- Full-time
- Microsoft Powerpoint
- Data analysis skills
- Analysis skills
- Free parking
- Employee assistance programme
Quick apply
21h
Senior Contract Manager
Hitachi —Stone
- Full-time
- Remote
- Sales
- Mentoring
- Contracts
- Flexible schedule
Regulatory Affairs Specialist (Technical Writing)
Biocomposites —Keele
- Full-time
- Microsoft Word
- Doctoral degree
- Data analysis skills
- Free parking
- Employee discount
Quick apply
14d
Senior Design Manager
Dandara —Altrincham
- Management
- CAD
- Microsoft Office
- Employee assistance programme
11h
Commercial Procurement Assistant - Energy & Natural Resource
Turner & Townsend —Warrington
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Office
- Analysis skills
Quick apply
Director, Patient Centered Outcomes Assessment
RTI International —Manchester
- Full-time
- Doctoral degree
- Master's degree
- Business development
Senior Cyber Operations Test Manager - AVP
Barclays —Knutsford
- Leadership
Manufacturing Engineer
Rapiscan —Stoke-on-Trent
- Engineering
- Data analysis skills
- Analysis skills
1d
Associate Data Scientist
Charles River Laboratories —High Peak
- £27,000 a year
- Full-time
- Data analysis skills
- Master's degree
- Continuous improvement
8d
Design Manager
Willmott Dixon —Warrington
- Hybrid work
- Team management
- Leadership
- Communication skills
Quick apply
2d
Radiology Research Manager
The Christie NHS Foundation Trust —Manchester
- £49,387 - £56,515 a year
- Full-time
- Organisational skills
- Communication skills
9d
Senior Manager Biocompatibility
Convatec —Didsbury
- Full-time
- Hybrid work
- Doctoral degree
- Master's degree
- Bachelor's degree
Principal Nuclear Safety Case Engineer
AECOM —Warrington
- Full-time
- Hybrid work
- Engineering
- Master's degree
- Bachelor's degree
Senior Nuclear Safety Case Engineer
AECOM —Warrington
- Full-time
- Hybrid work
- Engineering
- Master's degree
- Mentoring
Intermediate Business Analyst
CDL Software —Manchester
- £40,000 - £45,000 a year
- Full-time
- Hybrid work
- Analysis skills
- Software development
- AI
- Free parking
- Referral programme
Quick apply
Payroll Specialist
Gray Healthcare Ltd —Macclesfield
- £38,000 - £40,000 a year
- Full-time
- Microsoft Excel
- Organisational skills
- Communication skills
- Free parking
Quick apply

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regulatory project manager jobs near alsager, chs

Clinical Project Manager

Biocomposites -
Keele

Quick apply

Job details

Full-time
1 day ago

Benefits

Free parking
Company pension
Company events
Free or subsidised travel
Employee discount
On-site parking

Qualifications

Healthcare research operations
Clinical research
Stakeholder collaboration
Stakeholder liaison
Internal department liaison
Project team management
Product development
Organisational skills
Project schedule tracking
Multidisciplinary collaboration
Good Clinical Practice (GCP)
Leadership
Project management experience
Team motivation leadership
Communication skills
Good Clinical Practice (ICH-GCP) guidelines
Project progress tracking
Progress tracking

Full job description

Job Description

Biocomposites is an international medical devices company that engineers, manufactures, and markets world leading products for use in infection management in bone and soft tissue. Based in Keele, UK, it has global operations across Europe, USA, Argentina, Canada, China, and India. Biocomposites is a world leader in the development of innovative calcium compounds and bone cements for surgical use. Its products regenerate bone and target infection risks across a variety of specialties, including musculoskeletal infection, orthopaedics, trauma, spine, foot and ankle, podiatry, and sports injuries. Biocomposites products are now used in over one million procedures per annum and sold in more than 100 countries around the world.

Job Summary

The Clinical Project Manager is a key part in a product development program from concept through to commercial product. The role requires working closely with other departments in Biocomposites, including research, regulatory, quality, manufacturing, and finance. The role also requires the individual to work closely with contractors, including research laboratories and clinical research organisations.

The postholder will provide dedicated oversight of the clinical studies commissioned by Biocomposites, involving planning, organizing, and directing the activities of personnel involved in clinical research projects to make sure that they deliver in line with the clinical goals and objectives.

The Clinical Project Manager will act as the primary contact for vendors and will lead in planning and communication with diverse study teams to make sure that trials are conducted and executed effectively. They are also responsible for the preparation and review of all documents that are related to clinical projects, which includes contracts, vendor budgets, regular updates and annual reports.

Reports to

Clinical Research Director

Location & Working pattern

Keele Office - Monday to Friday 9am to 5pm, 35hpw

Duties & Responsibilities

Work closely with the Clinical Research Director to develop and execute the Project Plan
Act as project Manager to ensure effective project management, providing timely issue resolution, expert knowledge and key decisions at each stage of the project
Manage adherence to project budgets
Report and communicate project progress on a regular basis to key stakeholders
Provide regular reports, quantifying progress, performance, cost and associated internal risk relative to the achievement of project goals
Establish and maintain key relationships with internal and external stakeholders
Negotiate and Influence key stakeholders at all levels in line with business and programme requirements and ensure that productive and effective relationships are maintained
Demonstrate creativity and innovation on projects by maintaining up to date knowledge of advances in project management techniques
Monitor and report on the progress of delegated clinical trials, which includes budgets and timelines
Prepare, oversee, and review documents that are related to assigned clinical study
Ensure the availability of necessary resources for the execution of clinical projects
Review and approve invoices being presented by study vendors and external consultants
Answerable to questions and issues brought up by vendors and external consultants
Fully involved in resolving issues and contribute to improvement strategies for delivery of future studies
Work with other members of the study team to outline priorities, and resolve conflicts that may come up in the project process

Essential requirements

A minimum of 5 years experience in the field of clinical research of which 2 years must have been in a project lead role
Experience in writing clinical study procedures and other clinical documents
Delivery of Site Initiation Training for clinical trials
In depth knowledge of ICH GCP
Able to convey information to clinical investigators, clinical trial sites and CROs
Ability to organise and motivate other members of the study team.
Must be able to work as part of a team.
Must possess excellent communication skills so as to be able to effectively convey messages across to both study team members and other external persons like vendors and external consultants.
Good problem-solving, organizational, and leadership skills are highly required.
Ability to pay keen attention to detail at all times.
Must be able to work within stipulated timeframes or deadlines even in the face of multiple responsibilities or projects

Desirable requirements

Medical, nursing or scientific degree
Protocol writing
Knowledge of IRB submissions

What do we offer?

Competitive salary and benefits! With us, you will receive a competitive salary package and benefits.

We grow talent. At Biocomposites we create opportunities to thrive and grow.

One Biocomposites – team spirit & engagement. Our culture is important and we strive to create engaged and inclusive global teams that encourage colleagues to share their diverse perspectives and opinions.

Who do we look for?

People who are passionate about what we do.

People who are open minded to evolving the way we work.

People who can work together to transform outcomes and change lives.

Benefits:

Company events
Company pension
Employee discount
Free or subsidised travel
Free parking On-site

Quick apply

Refine Your Search

regulatory project manager jobs in alsager, chs

Clinical Project Manager

Senior Project Manager

Client Services Manager

Risk Management Specialist

Sustainability and Ethics Officer

Senior Contract Manager

Regulatory Affairs Specialist (Technical Writing)

Senior Design Manager

Commercial Procurement Assistant - Energy & Natural Resource

Director, Patient Centered Outcomes Assessment

Senior Cyber Operations Test Manager - AVP

Manufacturing Engineer

Associate Data Scientist

Design Manager

Radiology Research Manager

Senior Manager Biocompatibility

Principal Nuclear Safety Case Engineer

Senior Nuclear Safety Case Engineer

Intermediate Business Analyst

Payroll Specialist

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