Senior Site Contract Associate - Biotech
iqvia · Paris
Job description
About the role
IQVIA Biotech supports biotech and emerging biopharma companies in clinical development across all phases and therapeutic areas. This Senior Site Contract Associate position covers France, Spain, Portugal and Greece and is home-based. You will support the delivery of start-up contracting activities for selected sponsors, studies or multi-protocol programs, including pre-award work.
Key responsibilities
- Develop simple investigator grant estimates and proposal text to support proposal development.
- Maintain contract and budget templates, contracting systems, tools, processes and training materials according to the Scope of Work and Project Plan.
- Collaborate with sponsors, stakeholders and RSU regions and countries to deliver the project scope in line with sponsor requirements and the RSU Management Plan.
- Provide operational and financial contracting support to facilitate business development and the initiation and maintenance of clinical trials while meeting regulatory requirements.
- Help create and review core scientific, technical and administrative documentation needed for study initiation and maintenance.
- Contribute to collecting, interpreting and sharing contracting intelligence for assigned studies and the wider company.
- Ensure contracting efficiency, adherence to timelines and financial goals, and report performance metrics and out-of-scope activities.
- Comply with contract management and quality standards and support contract analysts, managers and directors administratively.
- Maintain internal systems, databases, tracking tools, timelines and project plans, with emphasis on CTMS.
Required profile
- Bachelor's degree in life sciences or health care.
- At least 6 years of relevant experience, including demonstrable experience as a contract negotiator.
- Sponsor or clinical research organization clinical site contracting experience.
- Understanding of the regulated clinical trial environment and the drug development process.
- Ability to build effective working relationships with colleagues, managers and sponsors.
Required skills
- Good negotiating, communication and interpersonal skills, and strong technical writing.
- Knowledge of GCP/ICH and applicable regulatory guidelines, SOPs and corporate standards.
- Strong knowledge of Microsoft Office and e-mail applications.
- Ability to interpret pricing models and prepare proposals, bid grids and budgets.
- Good organizational and planning skills.
Questions fréquentes
Why are you reporting this job?
Explore further
Salaries, guides and searches in France.
Salaries by job title
- Aide ménager / aide ménagère (H/F) – CDI temps partiel 20
- Technicien de maintenance industrielle 14
- Employé(e) de ménage – CDI temps partiel 13
- Technicien de Maintenance Itinérant H/F 12
- Technicien de maintenance 11
- Employé(e) de ménage à temps partiel 10
- Conducteur de ligne H/F 8
- Collaborateur Comptable 8
Apply in 30 seconds
Enter your email to apply. An account will be created automatically.
By continuing, you accept our terms of use.
Already have an account? Login
A question about this job?
Ask it here: you will get the full job summary by e-mail, right away.
Published 10 hours ago
Expires 1 month from now
2 views · 0 interested
Boost your chances
Upload your CV — we will match you with relevant openings.
Analyzing your CV...
iqvia
Paris
Related job offers
-
Experienced Clinical Research Associate (CRA II / Senior CRA)
icon Paris -
Experienced Clinical Research Associate (CRA II / Senior)
icon Paris -
Registered Dietitian – Clinical Research Support (Remote, France)
iqvia Paris -
Manager, Feasibility & Site Activation
icon Warsaw -
CRA2 (Freelancer)
iqvia Illkirch-Graffenstaden