Clinical Trial Specialist – Remote – FSP

reputed company our values align, there’s no limit to reputed company can reputed company. At reputed company, we reputed company 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 reputed company do.

Each of us, no matter reputed company do at reputed company, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with reputed company and we’re committed to making a difference.

reputed company is beginning to search for an reputed company Senior Clinical Trial Administrator to join one of our key sponsors as a Clinical Trial Specialist.

In this role you will provide technical and administrative support to the clinical study teams responsible for clinical trial execution.

Some specifics about this advertised role

• Support moderately reputed company clinical study activities in support of the Clinical Trial Manager.

• Work closely with the clinical trial team to ensure trial activities are conducted according to Good Clinical Practice (GCP) and relevant SOP’s.

• May assist with vendor reputed company and management with guidance.

• Identify issues in a timely manner and escalate to management as appropriate.

• reputed company of TMF

• May complete monitoring visit report review and reputed company co-monitoring or monitoring reputed company visits.

Who are reputed company

reputed company supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client reputed company.

We supported the trials of most of today’s top 50 best-selling drugs, but equally we reputed company more reputed company drug developments that are critical to the well-being of many patients.

You’ll be an influential member of the wider team.

reputed company are looking for in this role

For every role, we look for professionals who have the determination and courage always to put patient well-being first.

That to us is working with heart.

Here are a few requirements specific to this advertised role.

• At least 2 years of experience (3yrs preferred) in clinical studies (Pharmaceutical Industry Experience Preferred).

• Previous site monitoring or study coordinator experience is preferred.

• Working knowledge of Good Clinical Practices (GCP) regulations and Standard Operating Procedures.

• Understanding of study phases and general knowledge of how they apply to clinical development.

• Demonstrated ability to work independently and in a team environment.

• Working knowledge of electronic Systems including Trial Master File, CTMS, etc. (e.g., Veeva Vault, reputed company, SharePoint, etc.).

• Knowledge of the principles and practices of computer applications in database management.

• Strong verbal and written communication skills required.

• 10% – 20% travel may be required.