Clinical Trial Assistant at Parexel

, , China -

Full Time

Start Date

Immediate

Expiry Date

21 Mar, 26

Salary

0.0

Posted On

21 Dec, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Trials, Regulatory Compliance, Database Management, Clerical Duties, Vendor Management, Communication, Organizational Skills, Time Management, GCP-ICH Guidelines, Clinical Development, Interpersonal Skills, Administrative Support

Industry

Pharmaceutical Manufacturing

Description

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. The Clinical Trial Administrator (CTA) is responsible for performing a variety of research, database, and clerical duties of a complex and technical nature in support of multiple clinical trials. This position also provides administrative support to clinical teams by reviewing vendor invoices for accuracy against budget, tracking vendor payments in compliance with federal regulations and taking meeting minutes during project team meetings. Bachelor’s degree in a related field, or equivalent combination of training, education and work experience, preferred • Three (3) or more years of experience in a clinical administrative or regulatory role in a pharmaceutical or CRO environment • Knowledge of FDA GCP-ICH Guidelines and local regulatory requirements • Knowing the objectives of the various stages of clinical development • Ability to demonstrate a high level of competency relating to administrative and clerical responsibilities, procedures, and systems • Excellent verbal and written communication, interpersonal, organizational, and time management Parexel is a leading global clinical research organization (CRO) providing insights-driven Clinical and Consulting solutions to the world’s life sciences industry. Leveraging deep local knowledge and a global breadth of clinical, regulatory and therapeutic expertise, our professionals worldwide work in partnership with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind — broadening access and making clinical research a care option for anyone, anywhere. Our proven track record spans 40+ years and drives us forward, advancing clinical research in healthcare’s most complex areas while harnessing innovation to drive efficiencies across every phase of the clinical development process. Our insights-driven approach, proven delivery and trusted execution are accelerating the delivery of life-changing treatments to patients — With Heart.™

Responsibilities

The Clinical Trial Assistant is responsible for performing a variety of research, database, and clerical duties in support of multiple clinical trials. This includes reviewing vendor invoices, tracking payments, and taking meeting minutes.