Peachtree BioResearch Solutions, a Julius Clinical Company, is a global specialized full-service CRO providing highly specialized study operations teams for pharmaceutical, biotech, and medical device companies. Formed over 15 years ago by a pharma leadership team experienced in buying CRO services with the purpose of creating trusting partnerships with sponsor clients - no matter their budget. We do this by investing in people who thrive in an environment where their experience and contributions can be felt throughout the organization. It's an exciting time as we expand our global reach, while still offering a personalized approach to sponsors and delivering incredible value.
We are looking to engage a US-based contractor who can act as a site contracts specialist and be responsible for negotiating and managing clinical site agreements and other related docs. This role will require less than a full-time commitment, and is 100% remote. You would work with highly experienced team members who are also very supportive.
Responsibilities:
- Negotiate clinical study budgets and clinical trial agreements (CTAs) with investigators or designated site personnel.
- Maintain a tracking system of clinical study agreements, issues and communications with internal and external sources regarding contract and budget status.
- Participate in clinical study team meetings, kick-off meetings, bid defense meetings and departmental/company meetings as needed.
- Develop relationships with Sponsors and Investigator Sites to facilitate effective communication and achieve favorable terms.\
- Provide input into contract template development.
- Assist with the negotiation and finalization of other contract types as may be assigned.
Experience:
- Experience in negotiation of investigator site contracts.
- Strong Excel knowledge and some experience with costing tools.
- Prior CRO experience highly desired
- Medical, Dental, Vision, Life, Disability coverage
- 20 days PTO + PTO rollover + 13 paid holidays
- 401(k)
Top Skills
What We Do
Over 10 years ago, Peachtree was founded to fill a perceived missing principle in typical CRO services. Where can I find a CRO that will partner with me, understand my challenges, and solve issues to keep my program on track? Filling this need requires experienced clinical research professionals.
We focused on people – building an organization by investing in highly experienced personnel with broad therapeutic area expertise in a number of clinical trials. From single-center Phase I to global multi-center trials. Most all of our clinical personnel have both sponsor and CRO experience – allowing us
to fully understand the issues our sponsor-clients face. We built a rock-solid processes and systems infrastructure to support the teams and this investment continues today – always seeking to improve our service.
We also saw the opportunity to support an under-served segment of the market – emerging mid-sized companies. We felt they could benefit from access to highly-experienced teams that understand the challenges of limited resources and be flexible, reliable, and responsive. Most of all – provide solutions.
So where is Peachtree today?
A full-service CRO offering project management, feasibility & subject recruitment, clinical site management & monitoring, data management, biostatistics, medical monitoring, medical writing, and
clinical quality assurance
We are 80+ highly-experienced clinical research professionals with an average of more than 20 years relevant clinical experience
Our client roster continues to grow having worked with nearly 100 pharmaceutical, biotech, and medical device companies providing full-service clinical trial support to niche services
Continued investment in best-in-class systems such as IBM Clinical for EDC, Veeva Vault for eTMF, ZenQMS for quality management and training, and Oracle for CTMS
