Clinical project manager Work, Jobs in Tongham, Sry (with Salaries)

Sr. Clinical Project Manager (Europe)
Allucent —Bracknell
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Flexible schedule
- Referral programme
Quick apply
Senior Clinical Data Manager - sponsor dedicated - oncology
Fortrea —Maidenhead
- Full-time
- Remote
- Presentation skills
- Mentoring
- Leadership
Project Manager, eCOA
IQVIA —Reading
- Full-time
- Remote
- PMP
- Public speaking
- English
- Work from home
Patient & Site Engagement Operations Manager - Sponsor Dedicated (m/w/d)
IQVIA —Reading
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- Data analysis skills
- Work from home
Clinical Registry Coordinator
ICON Plc —Reading
- Full-time
- Remote
- Microsoft Office
- Project management
- Bachelor's degree
- Employee assistance programme
6d
Site Activation Specialist
IQVIA —Reading
- Full-time
- Remote
- Travel
- Contracts
- Negotiation
- Work from home
Senior Manager, Clinical Data Management
Bristol-Myers Squibb —Uxbridge
- Full-time
- Hybrid work
- PMP
- Project management
- Presentation skills
Local Study Associate Director
IQVIA —Reading
- Full-time
- Remote
- Patient monitoring
- English
- Project management
- Work from home
14d
ECOA Project Manager
ICON Plc —Reading
- Full-time
- Remote
- Management
- Project management
- Presentation skills
- Employee assistance programme
7d
Manager, Clinical Study Lead
Regeneron —Uxbridge
- Microsoft Powerpoint
- Microsoft Word
- Bachelor's degree
- Annual leave
RWE Alliance Manager (FSP)
IQVIA —Reading
- Full-time
- Remote
- Project management
- Bachelor's degree
- Continuous improvement
- Work from home
5d
CDC Trial Manager I
Novo Nordisk —Gatwick Airport
- Computer literacy
- English
- No degree
9d
Project Manager, IRT
ICON Plc —Reading
- Full-time
- Project management
- Bachelor's degree
- Travel
- Work from home
- Employee assistance programme
8h
Senior Clinical Programmer I
Allucent —Bracknell
- Full-time
- Hybrid work
- Computer Science
- Bachelor's degree
- Flexible schedule
- Referral programme
Quick apply
Clinical Trials Manager
Gilead Sciences —London
- Full-time
- Management
- Doctoral degree
- Master's degree
Senior Coordinator
IQVIA —Reading
- Full-time
- Hybrid work
Redevelopment Senior Project Manager
The Hillingdon Hospitals NHS Foundation Trust —Uxbridge
- £66,582 - £77,368 a year
- Full-time
- Project management
3h
Senior Program Portfolio Manager
Durbin PLC (UK) —Middlesex
- Hybrid work
- Project management
- Bachelor's degree
- Leadership
- Work from home
- Employee assistance programme
Quick apply
12d

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Sr. Clinical Project Manager (Europe)

Allucent -
Bracknell

Quick apply

Job details

Benefits

Flexible schedule
Referral programme

Qualifications

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Clinical research
ADP
English
Administrative experience
Analysis skills
Project management
Bachelor's degree
Organisational skills
Business
Financial acumen
Communication skills

Full job description

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.

We are looking for a Sr. Project Manager (Sr. PM) to join our A-team (hybrid*/remote). As a Sr. PM at Allucent, you are responsible for the overall coordination and management of clinical trials from start up through to final delivery. The trials are mainly in Oncology, Neuroscience or Immunology and Infectious Diseases. Experience in Cell and Gene Therapy is a plus. This position directs the technical and operational aspects of clinical projects - all with the sense of urgency expected of Allucent customers.

In this role your key tasks will include:

Leads the project team, ensuring the project is delivered according to planned scope and timelines in accordance with the contract
Creates and executes project management plans required for project delivery and in accordance with established processes
Ensures quality and adherence to the relevant policies, SOPs, and working instructions, GCP and regulatory guidelines.
Establishes clear communication lines and escalation pathways, communicates with project stakeholders
Provides input on study related documents such as the study protocol, CRF, Medical Review/Monitoring plan, and Clinical Study Report
Establishes requirements for and ensures project specific training plan for team activities
Leads internal and external meetings, with internal and sponsor teams, including Kick Off Meetings (KOM) and Investigator Meetings based on project scope
Provides support for vendor identification, qualification and selection and manage vendors
Manages vendors and vendor relationships as required for project delivery
Ensures effective and efficient resource utilization across projects and programs
Produces, maintains and circulates project progress and status reports
Manages the study budget, including monthly invoicing.
Establishes project risk management plan with input from client and functional stakeholders and oversees adherence and updates throughout the project lifecycle
Proactively recognizes and addresses any changes in scope
Negotiates and influences internal and external team members in a professional manner and with successful outcomes
Effectively solves problems with projects teams by applying strategic thinking and conflict resolution skills
Ensures the Trial Master File is kept up to date and inspection ready
Serves as the primary point of communication between the sponsor and project team
Leads by example and encourages team members to develop strong solutions for clinical trial delivery
Responsible for oversight of project team delivery and communication with functional managers, including performance feedback

Requirements

To be successful you will possess:

Minimum Bachelor’s degree in life science, healthcare and/or business degree
Minimum 5 years of relevant work experience
Minimum 5 years of experience in drug development and/or clinical research, with at least 3 years of clinical trial project management experience
Preference for candidates with CRA experience
Expert knowledge of ICH-GCP(R2), data and patient privacy practices, and applicable (local) regulatory requirements
Demonstrates strong financial acumen, administrative excellence and analytical skills
Experience managing all phases of the full-service clinical trial delivery lifecycle (Start-up, Maintenance, Close-out).
Excellent written and verbal communication, planning, critical thinking and organizational skills, including command of English language
Representative, outgoing and client focused
Ability to work effectively in a fast-paced challenging environment with a growing company
Proficiency with various applications including, but not limited to, Microsoft Word, Excel, and PowerPoint required
Strong presentation skills
Fosters learning and the advancement and development of others
Dependable and able to take action to quickly to address urgent needs
Proactive and solution oriented
Willingly takes ownership and drives positive, collaborative results with the project team
Exercises good judgement with defined procedures and policies to determine appropriate action

Benefits

Benefits of working at Allucent include:

Comprehensive benefits package per location
Competitive salaries per location
Departmental Study/Training Budget for furthering professional development
Flexible Working hours (within reason)
Opportunity for remote/office* working depending on location
Leadership and mentoring opportunities
Participation in our Buddy Program as a new or existing employee
Internal growth opportunities and career progression
Financially rewarding internal employee referral program
Access to online soft-skills and technical training via ADP and internal platforms

Disclaimers:

Our office work policy encourages a dynamic work environment, prescribing 2 days in office per week for employees within reasonable distance from one of our global offices.

“The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.”

#LI-AdT #LI-remote #LI-hybrid

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Refine Your Search

clinical project manager jobs in tongham, sry

Sr. Clinical Project Manager (Europe)

Senior Clinical Data Manager - sponsor dedicated - oncology

Project Manager, eCOA

Patient & Site Engagement Operations Manager - Sponsor Dedicated (m/w/d)

Clinical Registry Coordinator

Site Activation Specialist

Senior Manager, Clinical Data Management

Local Study Associate Director

ECOA Project Manager

Manager, Clinical Study Lead

RWE Alliance Manager (FSP)

CDC Trial Manager I

Project Manager, IRT

Senior Clinical Programmer I

Clinical Trials Manager

Senior Coordinator

Redevelopment Senior Project Manager

Senior Program Portfolio Manager

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