Site Specialist

PPD-Pharmaceutical Product Development is looking for an energetic and highly organized Site Specialist to join our team. Our ideal candidate is a collaborative problem-solver with a high attention to detail and a commitment to providing exceptional customer service. If you have the qualifications listed below and are excited to join a fast-paced, ever-evolving industry, then we want to hear from you!Required Qualifications:• Bachelor's degree in a scientific or related field• At least 2 years of experience in clinical research• Understanding of Good Clinical Practice (GCP) and ICH guidelines• Excellent written and verbal communication skills• Ability to manage multiple projects simultaneously• Proficiency in MS Office applications and data entry programs• Knowledge of clinical trial processes and procedures

Responsibilities:

1. Work with project teams to ensure compliance with Good Clinical Practice (GCP) and ICH guidelines.
2. Monitor clinical trial data and ensure accuracy and completeness of documentation.
3. Liaise with sponsors and clinical sites to facilitate the smooth running of clinical trials.
4. Support the development of processes, procedures and SOPs.
5. Prepare and maintain clinical trial documentation, such as protocols, Informed Consent Forms and Case Report Forms.
6. Assist with data entry and data management activities.
7. Monitor and track clinical trial progress against timelines.
8. Manage project budgets and ensure timely delivery of deliverables.
9. Provide customer service to sponsors, clinical sites and other stakeholders.
10. Monitor and track project milestones and prepare reports.

According to JobzMall, the average salary range for a Site Specialist is $45,000 to $65,000 per year. This range depends on the size of the company, the experience of the individual, and the scope of the job duties.

PPD, Inc. is a global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services.