Site Contracts Specialist, Hybrid in Munich, Sponsor-dedicated, Germany

**Description**

**Site Contracts Specialist, FSP, client-dedicated, hybrid in Munich**

Come discover what our 25,000+ employees already know: work here matters everywhere. We're a growing and evolving biopharmaceutical industry leader, which means you'll have endless opportunities to work with experts around the world and build the career you've dreamed of.
As a part of the Syneos Health team, you'll help us deliver results for a rewarding reason - we improve patients' lives around the world. Because to us, a patient isn't just a number, they're our family, friends, and neighbors.

**Why Syneos Health**
- #SyneosHealthLife means we're committed to our Total Self culture - where everyone can authentically be themselves. Our Total Self culture is what unites us globally, and we know every person's unique contributions make a difference.
- We believe our success is a direct result of the people who are driving it - you We value your dedication to care for our customers and patients, so we want to focus on taking care of you. That's why we offer a comprehensive benefits program encompassing your total health - physical, mental and financial.
- We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we're able to create a place where everyone feels like they belong.

**Role Purpose**

Here at Syneos Health we are currently looking for a **Site Contracts Specialist**opening,**to work on a sponsor-dedicated role in a permanent full-time position. The role is 2x per week Munich office based and 3x per week home-based. You will need to visit the office just for printing purposes. The role is part of our FSP 360 team (functional service provider), which is designed to successfully meet the individual needs and goals of the client you will be supporting.

Responsible for the end-to-end management of budgeting and contracting for Study Teams with a focus on contracting a variety of contracts & study types including Confidential Disclosure Agreements (CDAs), Investigator contracts for client sponsored studies, non-registrational / Investigator Sponsored Research (ISR) studies.

**Key Responsibilities and Major Duties**
- Provide knowledgeable single-point of service to study teams related to study budgets and contracts
- Prepare study /site level grant budgets
- Manage the end-to-end process for executing Clinical Trial Agreements (CTAgs) with investigator sites
- Prepares contract documents from templates and modify to reflect unique aspects of the particular study, including (the CTAg financial appendix),
- Negotiates financial and legal aspects of CTAg and Master Service Agreements with sites, Institutions or vendor personnel
- Is trained on legal fall back language and works with Legal as needed.
- Communicates clearly and efficiently with client Clinical and Legal Teams regarding amendments and other issues
- Enter CTAg, documents and data into Clinical Trial Management System and contract management software and ensure correct filing.
- Preparation, negotiation and execution of Master Agreements with Institution
- Develop and maintain template language in collaboration with legal for all contract types. Would include maintenance of associated back-up language
- Escalate to appropriate client colleague when a significant risk to the business is identified
- Independently make appropriate business decisions within their scope or authority, and educate internal project leaders on the issues and risks associated with contracting decisions
- Ensure contracts are executed in alignment with trial deliverables and priorities
- Execute local purchase contracts if applicable (e.g. of drug, equipment)
- Ensure all CTAgs and payments are accurately posted and ensure correct filing
- May support preparing invoices/payments due reports and managing, tracking and executing payments to investigator sites

**Qualifications**

**What we are looking for**:

- BA/BS degree in Business Administration, Public Administration, Public Health, related field, or equivalent combination of education and experience. Advanced degree preferred. Fluent in German and English.
- 2 or more years' experience negotiating legal and/or financial agreements, preferably in pharmaceutical industry clinical trials or years of industry related experience in clinical operations
- Working knowledge of clinical trial start-ups and finance cycles including knowledge of site needs and perspective

Strong organization and time management skills and ability to effectively manage multiple competing priorities
Strong communication skills with a strong customer focus, able to manage both internal and external clients at all organizational levels
Strong negotiation and interpersonal skills including strong conflict resolution skills
- Experience with Clinical Trial Management Systems (CTMS), SAP and Contract Management So