Internal investigator Work, Jobs in Reading, Brk (with Salaries)

Manager, Investigator Site Budgets & Contracts
ICON Plc —Reading
- Full-time
- Remote
- Microsoft Excel
- Microsoft Office
- Contracts
- Employee assistance programme
4d
Clinical Research Associate II
IQVIA —Reading
- No degree
Senior Quality Assurance Manager (Clinical)
Bio Pharma Resourcing —Thames Valley
- £35,000 - £40,000 a year
- Travel
- Computer skills
Medical Director
ICON Plc —Reading
- Full-time
- Remote
- Patient monitoring
- English
- Communication skills
- Employee assistance programme
Senior Director, Search & Evaluation Late TA Lead, Immunology
CSL Behring —Maidenhead
- £263,000 - £328,000 a year
- Full-time
- Doctoral degree
- Master's degree
- Business development
Research Associate in Native Ambi...
The Rosalind Franklin Institute —Harwell
- £37,500 - £38,500 a year
- Full-time
- Doctoral degree
- Leadership
- Free parking
- Annual leave
4d
Global Data Manager - homebased (FSP)
IQVIA —Reading
- Remote
- Bachelor's degree
11d
Senior Clinical Trial Administrator
GE HEALTHCARE —Chalfont Saint Giles
- Travel
- Communication skills
Associate Project Manager - Cell and Gene Therapies m/w/d
UPS —London
- Project management
- Communication skills
Sr. Clinical Project Manager (Europe)
Allucent —Bracknell
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Flexible schedule
- Referral programme
Quick apply
Medical Strategy Lead, Oncology (Home-Based)
IQVIA —Reading
- Remote
- Microsoft Outlook
- English
- Business development
Clinical Trials Manager
Gilead Sciences —Uxbridge
- Full-time
- Hybrid work
- Travel
- Organisational skills
- Communication skills
Specialty Claims Crime Prevention Consultant
Allianz —Datchet
- £30,000 a year
- Full-time
- Hybrid work
- Customer service
- Organisational skills
- AI
- Employee discount
8d
Associate Director Inspection Management (GCP)
Regeneron —Uxbridge
- Supervising experience
- Presentation skills
- Bachelor's degree
- Annual leave
Medical Advisor
Norgine —Uxbridge
- Full-time
- Hybrid work
Quick apply
Manager, Clinical Study Lead
Regeneron —Uxbridge
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Bachelor's degree
- Annual leave
Associate Director, Medical Affairs
CSL Behring —Maidenhead
- Full-time
- Doctoral degree
5d
Assoc Director, Clinical Operations
Gilead Sciences —Uxbridge
- Full-time
- Hybrid work
- Management
- Doctoral degree
- Master's degree
Senior Manager, Clinical Data Management
Bristol-Myers Squibb —Uxbridge
- Full-time
- Hybrid work
- PMP
- Project management
- Presentation skills
8d
Principal Statistician (Pharmacokinetics)
PSI CRO —Oxford
- Full-time
- Remote
- English
- Master's degree
- Communication skills
Quick apply

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internal investigator jobs near reading, brk

Manager, Investigator Site Budgets & Contracts

ICON Plc -
Reading

Apply Now

Job details

Full-time
4 days ago

Benefits

Company pension
Employee assistance programme

Qualifications

Contract management
Microsoft Excel
Microsoft Office
Contracts

Full job description

Manager, Investigator Site Budgets & Contracts

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

As a Manager, Investigator Site Budgets & Contracts at ICON, requires a candidate with extensive experience using Grants Manager and/or GrantPlan and the ability to produce accurate Phase 1 – IV budgets efficiently. The ideal candidate will also provide valuable input into scenario planning and its impact on the study budget

What You Will Do:

You will focus on the generation and review of investigator site budgets related to investigator grants (IGs) using Grants Manager .

Key responsibilities include:

Responsible for creation & direct oversight/management of site budgets for multiple assigned clinical trials within designated therapeutic area.
Provide consistent site contract/budgets oversight and support to assigned Clinical Operations clinical trial teams, offering up-front and ongoing strategic planning specific to the program and needs of individual studies.
Leverage use of internal and CRO provided Investigator Grants (IG) reference data and available Fair Market Value (FMV) benchmarking tools to establish clinical trial-specific IG budget estimates for trial budget forecasting needs.
Lead and/or contribute to development of target FMV-based IG budget and negotiation parameters according to therapeutic area (infectious disease, oncology and/or therapeutics) in an outsourced CRO model.
Act as lead point of contact (POC) for CRO site budgets-related activities for assigned studies; oversee the development and approval of global investigator site budgets and associated negotiation parameters. Ensure cross-program/cross-clinical trial consistency in country-level site budget targets and parameters.
Responsible for direct management and tracking of CRO investigator site CTA/budget negotiations in alignment with FMV and GCP-driven principles.

Your Profile:

You will have solid contract management experience, with the ability to manage competing priorities and develop your team.

Required qualifications and experience:

Minimum 5 years’ direct experience in global investigator site budget creation and negotiations; strong experience in the use of GrantManager/GrantPlan; preferable experience in CTA template language negotiations and/or support in collaboration with Legal.
Effective communication and collaboration with key internal and external stakeholders, including CDO, CRO and investigator site personnel.
Strength in financial analysis and financial justification.
Familiarity in working within an outsourced model; experience in direct CRO oversight of CTA/budget negotiations.
Proficient in MS Office Products with advanced knowledge of Excel; ability to work with and be proficient in stand-alone system applications.
High level of attention to detail in management of high volumes of investigator site financial data

#LI-Remote

#LI-RS1

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Apply Now

Refine Your Search

internal investigator jobs in reading, brk

Manager, Investigator Site Budgets & Contracts

Clinical Research Associate II

Senior Quality Assurance Manager (Clinical)

Medical Director

Senior Director, Search & Evaluation Late TA Lead, Immunology

Research Associate in Native Ambi...

Global Data Manager - homebased (FSP)

Senior Clinical Trial Administrator

Associate Project Manager - Cell and Gene Therapies m/w/d

Sr. Clinical Project Manager (Europe)

Medical Strategy Lead, Oncology (Home-Based)

Clinical Trials Manager

Specialty Claims Crime Prevention Consultant

Associate Director Inspection Management (GCP)

Medical Advisor

Manager, Clinical Study Lead

Associate Director, Medical Affairs

Assoc Director, Clinical Operations

Senior Manager, Clinical Data Management

Principal Statistician (Pharmacokinetics)

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