Description
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 centers on the customer and the patient. We continually seek to simplify and streamline our work to make Syneos Health easier to work with and for.
Whether 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 therapy delivery because we are passionate about changing lives.
Discover what our 29,000 employees across 110 countries already know:
WORK HERE MATTERS EVERYWHERE
Why Syneos Health
We are passionate about developing our people through career development, support, training, peer recognition, and rewards.
We are committed to our Total Self culture, where you can be authentic. We take care of our people and foster diversity of thoughts, backgrounds, and perspectives.
Job Responsibilities
Perform activities in compliance with applicable policies, SOPs, and work instructions.
Assist Clinical Monitoring staff with site management, serving as a Sponsor representative, and communicating with sites to ensure compliance with protocols and guidelines.
Create and maintain project files, handle correspondence, participate in audits, and prepare site manuals and reference tools.
Maintain and update clinical tracking information, manage documents, and coordinate logistics for site supplies.
Assist with team meetings, prepare minutes, anticipate issues, and implement corrective actions.
Complete training to stay aware of clinical research developments.
Potentially provide training or mentorship to junior staff.
Qualifications
What we’re looking for
Associates degree preferred or equivalent; experience in clinical research or related field considered in lieu of degree.
Knowledge of medical terminology, clinical data, and ICH/GCP preferred.
Strong organizational, communication, and interpersonal skills.
Ability to prioritize tasks and embrace new technologies.
Minimal travel up to 10% may be required.
Get to know Syneos Health
We have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products, and over 200 studies across numerous sites and patients.
In any role, you’ll take initiative and challenge the status quo in a dynamic environment. Learn more about us.
Additional Information
Tasks and responsibilities are not exhaustive. The company may assign other duties at its discretion. Qualifications considered as equivalent will be evaluated accordingly. This description does not constitute a contract. We comply with all applicable legislation and are committed to equal opportunity employment, including reasonable accommodations under the ADA.
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