(LB-572) - Sr Site Contracts Lead With Clinical Trials Experience In Argentina Or Mexico

(LB-572) - Sr Site Contracts Lead With Clinical Trials Experience In Argentina Or Mexico

15 feb
|
Syneos Health
|
Xico

15 feb

Syneos Health

Xico

.Sr Site Contracts Lead with Clinical Trials Experience in Argentina or MexicoUpdated: February 10, 2025Location: Mexico-Latin America - MEX-Home-BasedJob ID:25001551Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.
We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.Our Clinical Development model brings the customer and the patient to the center of everything that we do.
We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with,



but to make us easier to work for.Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals.
We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.Job responsibilitiesEstablishes, 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.Provides 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.




Provides consultation during escalation of out-of-parameter queries as needed.Advises study team and Sponsor stakeholders on industry trends, norms, and emergent developments surrounding site contract and budgetary negotiations.
Provides consultation on potential risks and mitigation tactics for negotiation issues pertaining to overall study start-up needs.Acts as first-line subject matter expert for all such CTA elements on assigned studies for internal and sponsor stakeholders alike.
Advises stakeholders on issue resolution within the context of assigned studies.
May seek additional support from internal support structures as needed.Plans contract execution strategy for assigned studies—including forecast of site-specific contractual execution timelines with as much accuracy as possible—and coordinates with internal study team stakeholders to ensure that CTA strategy is aligned with overall study start-up plans and expectations overall.
Manages expectations of internal and sponsor study team regarding global CTA negotiations for assigned studies

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