Clinical Trials jobs in Scotland
- ICON PlcLivingston
- Knowledge and understanding of clinical study protocols and schedule of assessments.
- 2 or more years of experience in clinical research site contracting and…
- View all ICON Plc jobs - Livingston jobs - Contract Analyst jobs in Livingston
- Salary Search: Contract Analyst I salaries
- See popular questions & answers about ICON Plc
- Medpace, Inc.Stirling FK9 4TZ
- Knowledge of medical terminology, and an interest in clinical trials/drug development – desirable.
- Medpace is a full-service clinical contract research…
- View all Medpace, Inc. jobs - Stirling jobs - Project Assistant jobs in Stirling
- Salary Search: Project Assistant - Clinical Safety salaries in Stirling
- See popular questions & answers about Medpace, Inc.
- Medpace, Inc.Stirling FK9 4TZ
- Knowledge of medical terminology, and an interest in clinical trials/drug development – desirable.
- Medpace is a full-service clinical contract research…
- Medpace, Inc.Stirling FK9 4TZ
- 1+ years clinical trial safety experience.
- Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development…
- MedtronicEdinburgh
- Relevant experience in clinical selling.
- Spending time in the OR working alongside our clinical stakeholders providing customer education on the safe and…
- View all Medtronic jobs - Edinburgh jobs - Senior Sales Specialist jobs in Edinburgh
- Salary Search: Senior Therapy Sales Specialist salaries in Edinburgh
- See popular questions & answers about Medtronic
- Inuvi Health LtdEdinburgh
- Be a qualified registered doctor, with broad and current clinical experience.
- We work with a diverse range of clients across various industry sectors, including…
- Centre for Implant DentistryGlasgow G3 7HU
- Company car
- In this pivotal role, you will develop strategic partnerships with dental practice and manage referral pipelines.
Clinic Nurse - Private Healthcare Services
Often replies in 1 dayBruntsfield PharmacyEdinburgh EH10 4EQ- Employee discount
- Sick pay
- Bereavement leave
- Store discount
- Company pension
- Private medical insurance
- Can deliver clinical services confidently, safely and effectively.
- Managing the clinic booking calendar and your own clinical workload.
- Thermo Fisher ScientificBellshill ML4 3NJ
- Work is performed in an office/ laboratory and/or a clinical environment.
- Prepares, reviews and coordinates, under guidance, local regulatory submissions (MoH,…
- Thermo Fisher ScientificPaisley PA4 9RE
- This will require in-depth knowledge of clinical markets and a clear understanding of what clinical customers expect.
- Entering clinical trial sites into Marken’s internal database (where necessary).
- To coordinate and manage shipment bookings and transportation activities,…
- View all UPS jobs - Edinburgh jobs - Customer Service Representative jobs in Edinburgh
- Salary Search: Preferred Customer Associate salaries in Edinburgh
- See popular questions & answers about UPS
- Medpace, Inc.Stirling FK9 4TZ
- Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical,…
- View all Medpace, Inc. jobs - Stirling jobs - Study Manager jobs in Stirling
- Salary Search: Regulatory Submissions (Study Start-up) Manager salaries
- See popular questions & answers about Medpace, Inc.
- Medpace, Inc.Stirling FK9 4TZ
- Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical,…
- View all Medpace, Inc. jobs - Stirling jobs - Study Manager jobs in Stirling
- Salary Search: Regulatory Submissions (Study Start-up) Manager salaries
- See popular questions & answers about Medpace, Inc.
- Medpace, Inc.Stirling FK9 4TZ
- Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical,…
- CatalentBathgate EH48 2FY
- Pharmaceutical, biotechnology, clinical supply, or other regulated industry experience.
- Experience with ERP, master data, clinical supply, or distribution…
- View all Catalent jobs - Bathgate jobs - Operations Supervisor jobs in Bathgate
- Salary Search: Regional Supervisor, Global Operations UK/EU salaries in Bathgate
- See popular questions & answers about Catalent
- MedtronicEdinburgh
- Own the end-to-end data lifecycle, from clinical study data collection to clinical validation trials.
- Design and manage scalable data infrastructure across…
- View all Medtronic jobs - Edinburgh jobs
- Salary Search: Data Engineer salaries in Edinburgh
- See popular questions & answers about Medtronic
People also searched:
Contract Analyst I
Job details
Full job description
At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.
As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.
As a Contract Analyst I at ICON, you will prepare, verifying, and carrying out invoicing via electronic processing and reporting activities for an assigned portfolio of accounts.
What You Will Do:
You will contribute to contract management activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
- Negotiate directly with assigned sites on all site related contracting items including clinical trial agreements, budgets, payment terms, ancillary agreements and amendments.
- Partner with internal Study Startup team, CROs, Clinical Operations teams, and TAU partners to improve overall SB&C metrics and deliver processes.
- Ensure standards are applied to the SB&C processes across projects.
- Leverage leading industry tools and data sources to provide budget and contract feedback aligned with parameters and fair market value guidance.
- Promptly recognize and improve potential delays and escalate to appropriate team members.
- Track all actions and negotiations to ensure timelines are achieved for studies and sites assigned.
- Support resolving escalated issues identified by the site activation sub-team in partnership with the internal Study Startup team.
Your Profile:
You will bring relevant contract management experience, along with the following qualifications and skills.
Required qualifications and experience:
- BS degree or international equivalent
- 2 or more years of experience in clinical research site contracting and budgeting within a pharmaceutical company, CRO or relevant industry vendor.
- Ability to explain data to facilitate decision making processes to be data driven.
- Knowledge and understanding of clinical study protocols and schedule of assessments
- Strong organizational skills, decision making, communication and negotiation skills.
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 .
Are you a current ICON Employee?