Clinical Development

Here in Clinical Development, we are passionate about collaborating and innovating as a team to help our customers achieve their goals. We know that the work we do matters, and we are driven to accelerate the delivery of therapies, because we are passionate to change lives.

Whether you’re a Clinical Research Associate, Clinical Trial Manager, Project Specialist, Project Manager or Director or work in Study Start Up; we all work in sync to deliver results and bring therapeutics to the patients that need them.

 

Find Your Fit

Discover where you belong in Syneos Health.

Clinical Research Associate

Clinical Research Associates (CRA) have a vital role in our clinical trials.

We perform monitoring and site management activities for Phase I-IV clinical research projects. Our job is to assess the progress of clinical projects at assigned sites (either on site or remotely) and to ensure clinical projects are conducted, recorded, and reported in accordance with the protocol, Syneos Health and Sponsor standard operating procedures and all applicable local and federal regulatory requirements.

Our CRAs are passionate about changing lives, and they so every day here at Syneos Health.

Project Specialist

At Syneos Health our Project Specialists (PS) are responsible for maintaining and coordinating the logistical aspects of clinical projects and provide overall support to functional leads to ensure the successful completion of project deliverables.

As Project Specialists we ensure the contracted services and expectations of assigned projects are carried out by the project teams in accordance with executed contracts and the customers’ requirements.

We do all of this whilst maintaining timely and effective communication among team members, site staff and providing support for quality assurance activities, including preparation for audits and internal review, preparing documentation and follow through to resolution.

You’ll partner with a diverse team of experts and collaborate with passionate problem solvers.

Study Start Up

In Study Start Up (SSU) we support the start-up process and manage the critical path to site activation. SSU is one of the most complex and heavily regulated parts of any clinical trial or program launch. This period involves a significant number of stakeholders at start-up sites, regulatory agencies, vendors as well as the customer.

Working efficiently in SSU, we help reduce the time it takes for patients to start their clinical trial journeys and help bring lifesaving treatments to those that need them.

Our People

 

Grace
Director Clinical Development

I am proud to be a part of the Oncology team at Syneos Health. The meaningful work and great people around me motivate & inspire me every single day. Developing new medicines is a long journey- innovation and creative thinking helps us to shorten the distance from lab to life.

 

Hear why William joined Syneos Health.

 

 

 

Functional Service Provider (FSP)

An FSP relationship is a partnership between a CRO and a Sponsor. Every partnership is unique with each one tailored to achieve our customer’s visions and goals. This allows us to grow and evolve with our customers as their portfolio needs evolve.

For Syneos Health it means that colleagues who like structure and predictability, and who truly enjoy relationship building in the work environment, tend to thrive in FSP environments.

Sponsors look to Syneos Health for technical expertise. They expect our colleagues to be an extension of their team and to bring new ideas; demonstrate expertise in technology and processes; escalate recommendations for improvements and take opportunities to innovate. In other words, Syneos Health has a voice.

 

Kickstart Your Career

Explore some of our entry level roles and begin your career in Clinical Development.

  • Project Specialist

    As a Project Specialist you’ll help perform administrative and supportive activities assigned by the Project Lead to ensure the contracted services and expectations are carried out by the project team in accordance with executed contracts and the customers’ expectations.

  • Site Contracts Specialist

    Our Site Contract Specialists administer and negotiate site contracts that support projects within Clinical Operations on a global scale, with oversight from the SSU Country Manager. We ensure site contract documentation is in compliance with Sponsor and Company requirements. We partner with internal and external team members to implement solutions for project and/or individual site contract related problems. We establish strong working relationships with customer, internal project teams and sites. We ensure all relevant documents are submitted to the Trial Master File (TMF) as per Company Standard Operating Procedure (SOP)/Sponsor requirements.

  • Project Admin Specialist

    As a Project Administration Specialist, you’ll provide administrative and technical support to the Clinical Research Associates, Clinical Trial Managers & Project Specialist to assist with contracted services.

  • SSU Regulatory Coordinator

    Our SSU Regulatory Coordinators are responsible for aiding in the delivery of Site Start-Up (SSU) activities in one or more of the following functional areas: investigator site contracts, ethics and regulatory submissions, and essential documents required for site initiation. We help support projects within Clinical Operations on a global scale, with oversight from the SSU Country Manager and Central and Shared Services leadership. We are responsible for ensuring regulatory and site contract documentation complies with sponsor and Company requirements. We collaborate with internal and external team members to implement solutions for project and/or individual site contract related problems. Ensuring all relevant documents are submitted to the Trial Master File (TMF) as per Company Standard Operating Procedure (SOP)/Sponsor requirements.

Title

Location

Date Posted

 

Inside Syneos Health


Total Rewards

Our Values

Learning & Development

FAQ

Why Work Here

Diversity, Equity & Inclusion