Senior Site Contract Manager
We are seeking a highly skilled Senior Site Contract Manager to join our team. As a key member of our organization, you will be responsible for establishing and maintaining strong relationships with site contracts leads and negotiators.
About the Role
This is an excellent opportunity for someone who is passionate about delivering high-quality work in a dynamic environment. You will be working closely with internal stakeholders and sponsors to prepare site contractual templates, including payment terms and study-level negotiation parameters and processes.
* Establishes, maintains and updates training material for site contracts lead team and site contract negotiators.
* Serves as subject matter expert within the organization equipped to help resolve global site contracting issues, and escalation point within the Company for internal customers to seek assistance.
* Oversees negotiations of clinical study agreements (CTA's) on a study level and drives CTA document finalization and execution, including contractual language & terms, financial attachments, and investigator grant budgets in collaboration with a global team of site contract & budget negotiators.
Responsibilities
The successful candidate will have the following responsibilities:
1. Provide oversight of contact & budget negotiations status and manages escalation of out-of-parameter queries on budgetary and contractual requests to sponsor decision-makers in all regions of study conduct.
2. Advises study team and Sponsor stakeholders on industry trends, norms, and emergent developments surrounding site contract and budgetary negotiations.
3. Acts as first-line subject matter expert for all such CTA elements on assigned studies for internal and sponsor stakeholders alike.
Requirements
To be successful in this role, you will need:
* A BS degree in life sciences, a health-related field, or equivalent combination of education and experience.
* Strong experience in a CRO/pharmaceutical industry and related clinical trial expertise.
* Thorough knowledge of applicable regulations, drug development, and clinical project management procedures.
* Proficient in MS Office (Word, Excel, and PowerPoint), MS Project, Outlook, and Internet.
* Ability to handle multiple tasks to meet deadlines, delivering high-quality work in a dynamic environment.
About Us
We are committed to building a diverse, inclusive, and authentic workplace. If your past experience doesn't align perfectly, we encourage you to apply anyway.
We are an equal opportunities employer and welcome applications from all qualified candidates. Please note that we do not discriminate based on race, color, age, religion, marital status, ethnicity, national origin, sex, gender, gender identity, sexual orientation, protected veteran status, disability, or any other legally protected status.