Site Contracts Lead

Syneos Health is seeking a Site Contracts Lead to manage the negotiation and finalization of clinical study agreements (CTAs). This role is crucial for accelerating customer success in the biopharmaceutical solutions sector. Join a talented team that uses the latest technologies and advanced business practices to speed the delivery of important therapies to patients.

The Site Contracts Lead will collaborate with a global team, ensuring compliance with sponsor and company requirements, and driving the execution of CTA documents, including contractual language, terms, financial attachments, and investigator grant budgets.

If you are passionate about shaping solutions that can dramatically impact lives and thrive in a dynamic, inclusive culture, we encourage you to apply.

Company Overview

Syneos Health® is a leading fully integrated life sciences services organization built to accelerate customer success. We partner with innovators across the drug development and commercialization continuum, helping them navigate complexity and accelerate progress. Our culture is authentic, inclusive, and high-performance, driven by a purpose to deliver impactful solutions for customers and patients.

Quick Details

• Salary Range: Not Specified
• Job Type: Full-time
• Qualifications: BS degree in life sciences, a health related field, or equivalent combination of education and experience.
• Experience: 5 Year+

Key Responsibilities

• Oversee negotiations of clinical study agreements (CTA´s) on a study level and drive CTA document finalization and execution.
• Provide oversight of contract & budget negotiations status and manage escalation of out-of-parameter queries.
• Act as a subject matter expert for CTA elements on assigned studies for internal and sponsor stakeholders.
• Plan contract execution strategy for assigned studies and coordinate with internal study team stakeholders.
• Work closely with internal stakeholders and with Sponsor to prepare site contractual templates.

Requirements

• BS degree in life sciences, a health related field, or equivalent combination of education and experience.
• Preferred experience in a CRO/pharmaceutical industry and related clinical trial expertise or site start-up experience.
• Thorough knowledge of applicable regulations, drug development and clinical project management procedures.
• Good presentation, documentation and interpersonal skills. Proficient in MS Office, MS Project, outlook and Internet.
• Ability to handle multiple tasks to meet deadlines, delivering high quality work in a dynamic environment.
• Strong leadership skills; ability to teach/mentor team members.

Benefits

• Career development and progression opportunities.
• Technical and therapeutic area training.
• Inclusive culture where you can authentically be yourself.
• Opportunity to shape solutions that dramatically impact someone’s life.
• Work in a highly competitive and ever-changing environment.