Contracts Manager - Clinical Trial Services Location: Madrid, Spain Job Type: Regular Full-time Division: Precision for Medicine Business Unit: Clinical Solutions Requisition Number: 4558 We are seeking an accomplished Contracts Manager (clinical trial site agreements) to join our European team!
We are looking for candidates who have strong experience in Clinical Site Agreements across Europe.
In particular, experience in managing site agreements across multiple European countries would be strongly desirable.
Do you enjoy a new challenge, thrive in the details, and flourish in multifaceted environments?
If you are no stranger to taking charge and enjoy contributing to a project team that delivers, we have an opportunity for you to bring your expertise in budgets and contracts to a new level.
As a Contracts Manager, you will review, draft, negotiate, and track a variety of legal agreements including confidentiality agreements, master confidentiality agreements, clinical study agreements, and amendment agreements across various locations, mainly European ones.
You will actively take part in setting up contracting strategies for assigned projects and work closely with the Clinical Operations study team, playing a key role to ensure deliverables align with defined study timelines.
You will have: Strong relevant experience in drafting, reviewing, and negotiating Clinical Trial Agreements and vendor contracts, as well as management, control, and tracking of the contract process.
You will be fully responsible for Site Contract Management from setting up site contracting strategy to execution of contracts.
Experience within CRO, life science, biotech, or pharmaceutical industry is essential.
Experience interacting with Global institutions with a main focus on European ones.
Excellent organisational and communication skills and attention to detail.
Education/qualifications required: Graduate of a secondary education or equivalent degree; Minimum 4 years or more of experience in setting up contracting strategy, drafting, reviewing, and negotiating site Clinical Trial Agreements, vendor contracts, and site budget negotiation.
Possesses strong organisational/written communication skills and the ability to multi-task and prioritise in a fast-paced environment.
Executes time-sensitive matters while maintaining accuracy and attention to detail.
Exhibits high self-motivation, and is able to work and plan independently as well as in a team environment.
Demonstrates a high degree of professionalism, as evidenced by punctuality, ability to deliver on commitments, an understanding of the service culture, and positive interactions with customers and teammates, including good interpersonal skills.
Displays sound business judgment and a proactive, independent work style.
Is proficient in MS Office software programs and computer applications.
Handles sensitive issues with discretion.
Works well independently and cooperatively with others to achieve common goals in a virtual environment.
Develops, maintains, and strengthens relationships with others inside or outside of the organization who can provide information, assistance, and support.
Some domestic and occasional international travel including overnight stays.
#J-18808-Ljbffr
