Clinical project manager Work, Jobs in Hare Hatch, Brk (with Salaries)

Sr. Clinical Project Manager (Europe)
Allucent —Bracknell
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- English
- Flexible schedule
- Referral programme
Quick apply
Project Manager, eCOA
IQVIA —Reading
- Full-time
- Remote
- Microsoft Powerpoint
- Travel
- Communication skills
- Work from home
13d
Manager, Clinical Data Management
IQVIA —Reading
- Full-time
- Remote
- Databases
- Bachelor's degree
- Team management
- Work from home
6d
Manager, Clinical Study Lead
Regeneron —Uxbridge
- Bachelor's degree
- Continuous improvement
- Travel
- Annual leave
Senior Manager, Clinical Data Management
Bristol-Myers Squibb —Uxbridge
- Full-time
- Hybrid work
- PMP
- Presentation skills
- Bachelor's degree
Senior Clinical Data Manager - sponsor dedicated - oncology
Fortrea —Maidenhead
- Full-time
- Remote
- Presentation skills
- Mentoring
- Leadership
Data Team Lead
IQVIA —Reading
- Full-time
- Remote
- Bachelor's degree
- Mentoring
- Leadership
- Work from home
12d
Transformation Manager
Kingston and Richmond NHS Foundation Trust —Kingston upon Thames
- £55,524 - £62,652 a year
- Full-time
- Presentation skills
- No degree
- Training & development
- Employee assistance programme
4h
Data Team Lead, EMEA
IQVIA —Reading
- Full-time
- Remote
- Microsoft Word
- English
- Bachelor's degree
- Work from home
- Employee stock ownership plan
4d
Local Study Associate Director
IQVIA —Reading
- Full-time
- Remote
- English
- Bachelor's degree
- No degree
- Work from home
Principal Investigator
Velocity Clinical Research, Inc. —High Wycombe
- Full-time
- Travel
Quick apply
Snr Data Team Lead, EMEA
IQVIA —Reading
- Full-time
- Remote
- Bachelor's degree
- Continuous improvement
- Leadership
- Work from home
4d
Patient & Site Engagement Operations Manager - Sponsor Dedicated (m/w/d)
IQVIA —Reading
- Full-time
- Remote
- English
- Presentation skills
- Bachelor's degree
- Work from home
Senior Portfolio Manager
Durbin PLC (UK) —Middlesex
- Hybrid work
- Bachelor's degree
- Continuous improvement
- Team management
- Work from home
- Employee assistance programme
Quick apply
2d

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clinical project manager jobs near hare hatch, brk

Sr. Clinical Project Manager (Europe)

Allucent -
Bracknell

Quick apply

Job details

Benefits

Flexible schedule
Referral programme

Qualifications

Microsoft Powerpoint
Microsoft Word
Technical project or programme management experience
Healthcare research operations
Sourcing
Clinical research
Resource allocation planning
Stakeholder collaboration
Stakeholder liaison
English
Microsoft Office Suite
Project team management
Analysis skills
Bachelor's degree
Risk management
Conflict management
Organisational skills
Project schedule tracking
Good Clinical Practice (GCP)
Training & development
Business
Financial acumen
Project management experience
Communication skills
Good Clinical Practice (ICH-GCP) guidelines
Project progress tracking

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

Quick apply

Refine Your Search

clinical project manager jobs in hare hatch, brk

Sr. Clinical Project Manager (Europe)

Project Manager, eCOA

Manager, Clinical Data Management

Manager, Clinical Study Lead

Senior Manager, Clinical Data Management

Senior Clinical Data Manager - sponsor dedicated - oncology

Data Team Lead

Transformation Manager

Data Team Lead, EMEA

Local Study Associate Director

Principal Investigator

Snr Data Team Lead, EMEA

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

Senior Portfolio Manager

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