Project Manager, Oncology - Sponsor Dedicated
Syneos Health Commercial Solutions · Atlanta, GA
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FULL-TIME
Posted Aug 24, 2026
Job Description
## Project Manager, Oncology – Sponsor Dedicated
Syneos 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 we do.
In this role, you'll manage interdisciplinary clinical research studies as a project manager, ensuring compliance with GCP, relevant SOPs, and regulatory requirements. You'll act as the primary liaison between the company and the customer to ensure timely study launch, conduct, and closeout according to contractual agreements. Leading the project team, you'll ensure quality, timelines, and budget management while being accountable for the financial performance of each project.
You'll coordinate activities and deliverables of all study conduct partners, proactively identify and manage issues, and ensure studies are conducted in compliance with GCP and regulatory requirements. Responsibilities include accountability for all project deliverables, quality and completeness of the TMF, maintenance of study information on various databases and systems, and study management components of inspection readiness. You'll oversee development and implementation of project plans, plan and present at internal and external meetings, prepare project management reports, and develop contingency planning and risk mitigation strategies. Additionally, you'll develop strong relationships with current clients to generate new business and may participate in bid defense meetings and line manage team members.
### Qualifications
- Bachelor's Degree (or equivalent) in life sciences, Medicine, Pharmacy, Nursing, or equivalent combination of education and experience.
- Clinical research organization (CRO) and relevant therapeutic experience preferred.
- Strong knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory requirements.
- Strong organizational skills and ability to manage time and work independently.
- Direct therapeutic area expertise.
- Ability to embrace new technologies.
- Excellent communication, presentation, and interpersonal skills, both written and spoken.
- Ability to travel as necessary (approximately 25%).
This posting is for a possible upcoming opportunity. By expressing interest, you'll be added to our talent pipeline.
### Benefits
The role offers a company car or car allowance, health benefits including Medical, Dental, and Vision, Company match 401k, eligibility for Employee Stock Purchase Plan, potential commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Salary varies based on qualifications and experience.
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_This job was found on [bandana.com](https://www.bandana.com/?utm_source=jd_attribution&utm_medium=repost)_
Syneos 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 we do.
In this role, you'll manage interdisciplinary clinical research studies as a project manager, ensuring compliance with GCP, relevant SOPs, and regulatory requirements. You'll act as the primary liaison between the company and the customer to ensure timely study launch, conduct, and closeout according to contractual agreements. Leading the project team, you'll ensure quality, timelines, and budget management while being accountable for the financial performance of each project.
You'll coordinate activities and deliverables of all study conduct partners, proactively identify and manage issues, and ensure studies are conducted in compliance with GCP and regulatory requirements. Responsibilities include accountability for all project deliverables, quality and completeness of the TMF, maintenance of study information on various databases and systems, and study management components of inspection readiness. You'll oversee development and implementation of project plans, plan and present at internal and external meetings, prepare project management reports, and develop contingency planning and risk mitigation strategies. Additionally, you'll develop strong relationships with current clients to generate new business and may participate in bid defense meetings and line manage team members.
### Qualifications
- Bachelor's Degree (or equivalent) in life sciences, Medicine, Pharmacy, Nursing, or equivalent combination of education and experience.
- Clinical research organization (CRO) and relevant therapeutic experience preferred.
- Strong knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory requirements.
- Strong organizational skills and ability to manage time and work independently.
- Direct therapeutic area expertise.
- Ability to embrace new technologies.
- Excellent communication, presentation, and interpersonal skills, both written and spoken.
- Ability to travel as necessary (approximately 25%).
This posting is for a possible upcoming opportunity. By expressing interest, you'll be added to our talent pipeline.
### Benefits
The role offers a company car or car allowance, health benefits including Medical, Dental, and Vision, Company match 401k, eligibility for Employee Stock Purchase Plan, potential commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Salary varies based on qualifications and experience.
---
_This job was found on [bandana.com](https://www.bandana.com/?utm_source=jd_attribution&utm_medium=repost)_
Benefits
- Health insurance
- Dental insurance
- Paid time off
Additional Details
- City
- Atlanta
- State
- Georgia
- Country
- US
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