Clinical Site Contract & Budget Negotiator ( level 2 or Senior)
- Bulgaria
- ICON Strategic Solutions
- Regulatory Affairs
TA Business Partner
- Icon Strategic Solutions
About the role
This vacancy has now expired. Please click here to view live vacancies.
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
We are hiring experienced Site Contract Negotiators to work closely with our client, a leading pharmaceutical company.
This particular role is a client dedicated one where you will work exclusively on one sponsors trials and SOPs.
Overview of the role:
- Perform negotiation of legal terms and budget terms for Clinical Study Agreements (“CSA”) (i.e., investigator site agreements)
- Perform negotiation of legal terms and budget terms for amendments to CSAs
- Draft and negotiate ancillary site contracts (e.g. PI / Sub-I / department agreements /Study Coordinator) as required
- Produce and maintain site-specific templates where needed to support the targeted investigator site list, but limited to the sites within the studies assigned
- Recommend country-specific and site /entity-specific modifications to templates based on site and local regulatory requirements
- Utilize previously negotiated terms for existing contracts between same site/entity
- Prioritize to meet study timelines to minimize impact to planned Site Initiation Visit (SIV) dates.
- Perform quality control checks of contracts and amendments prior to upload to DocuSign for electronic
- Pre-populate site-specific budget items from prior negotiations following sponsor provided guidelines.
- Negotiate site budgets following sponsor principles document and comments & fallbacks
- Actively participate in per-subject cost development meeting.
- Provide country level expertise to budget related contract terms and conditions
To be successful in the role, you will have:
- BA/BS/BSc degree
- 2 years Industry experience managing clinical site contracts & budgets are required.
- Demonstrates effective time management skills; able to independently prioritize multiple tasks.
- Demonstrates the ability to work independently and use initiative to anticipate/resolve issues and complete tasks.
Benefits of Working in ICON:
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. See all locations Learn more about Our Culture at ICON
Day in the life
.jpg)
Teaser label
Inside ICONContent type
BlogsPublish date
01/17/2025
Summary
Five Reasons Why You Should Work at a Contract Research Organization Contract research organisations (CROs) play a pivotal role in advancing medical science, offering career opportunities that are
.jpg)
Teaser label
Career ProgressionContent type
BlogsPublish date
05/10/2024
Summary
Although many employers are returning to the office, we’re still seeing a mix of both video and in-person interviews in application processes. Early in 2020, the number of companies using video interv
.png)
Teaser label
IndustryContent type
BlogsPublish date
01/18/2024
Summary
Introduction to Regulatory Affairs in Clinical Research Regulatory affairs play a pivotal role in ensuring the safety, efficacy, and quality of pharmaceutical products and medical devices. In the
Similar jobs at ICON
Salary
Location
Europe
Department
Regulatory, Drug Safety/ Quality Assurance & Other roles
Location
Any EMEA Location
Area of interest
Europe ICON Full Service & Corporate Support Talent Acquisition
Business Area
ICON Strategic Solutions
Job Categories
Regulatory Affairs
Job Type
Permanent
Description
As a Manager, Regulatory CMC (lifecycle management) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. We are seeking 2 ro
Reference
2025-120133
Expiry date
01/01/0001
Author
Patrick HaleAuthor
Patrick HaleSalary
Location
Japan, Tokyo
Location
Osaka
Tokyo
Remote Working
Home or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Drug / Device Regulatory Affairs
Job Type
Permanent
Description
We are currently seeking a Regulatory Affairs Specialist to join our diverse and dynamic team. As a Regulatory Affairs Specialist at ICON, you will play a pivotal role in designing and analyzing clini
Reference
JR129971
Expiry date
01/01/0001
Author
Haruna YamabayashiAuthor
Haruna YamabayashiSalary
Location
Japan, Tokyo
Location
Osaka
Tokyo
Remote Working
Home or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Drug / Device Regulatory Affairs
Job Type
Permanent
Description
We are currently seeking a Regulatory Affairs Specialist to join our diverse and dynamic team. As a Regulatory Affairs Specialist at ICON, you will play a pivotal role in designing and analyzing clini
Reference
JR127716
Expiry date
01/01/0001
Author
Haruna YamabayashiAuthor
Haruna YamabayashiSalary
Location
Georgia, Tbilisi
Location
Tbilisi
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Regulatory Affairs
Job Type
Permanent
Description
Job Responsibilities: • Recognize, exemplify and adhere to ICON's values which centre around our commitment to People, Clients and Performance • As a member of staff, the employee is expected to embra
Reference
JR131117
Expiry date
01/01/0001
Author
Maya KatsarskaAuthor
Maya KatsarskaSalary
Location
Poland, Warsaw
Location
Sofia
Warsaw
Johannesburg
Remote Working
Home or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Regulatory Affairs
Job Type
Permanent
Description
Job Responsibilities:• Ensuring regulatory deliverables are performed in accordance with all relevant regulations, guidelines, policies and procedures within contractual timelines and budget with soun
Reference
JR129985
Expiry date
01/01/0001
Author
Maya KatsarskaAuthor
Maya KatsarskaSalary
Location
UK, Reading
Location
Sofia
Warsaw
Reading
Gdansk
Warwickshire
Swansea
Remote Working
Home or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Drug / Device Regulatory Affairs
Job Type
Permanent
Description
We are currently seeking a Regulatory Project Manager (RPM) to join our diverse and dynamic Regulatory Project Services (RPS) team. As an RPM at ICON, you will play a pivotal role in contributing to d
Reference
JR130377
Expiry date
01/01/0001
Author
Maya KatsarskaAuthor
Maya Katsarska