purpose of the job:
billion dollar clinical trial patient recruitment sector. Almost all clinical trials fall behind schedule the potential of a true marketplace for clinical trials. We leverage proven data science and performance and are interested in participating in clinical trials. Responsibilities and Duties: Calling patients in clinical trials and conducting a basic medical screening Discussing available trials with patients screening to evaluate a patients eligibility for a trial Transferring pre-qualified patients to clinics for
limited to:
advantageous
Significant experience of regulatory drug development, manufacture, commercialisation or equivalent
/>Knowledge of regulatory procedures and legislation for drug development, product registration, line extension
/>Knowledge of regulatory procedures and legislation for drug development, product registration, line extension
They also prepare reports for the manager and trial balances to assist the
accountants. They may
and completing VAT returns.
â Preparing trial balances.
â Collecting account information
They also prepare reports for the manager and trial balances to assist theaccountants. They may be required filing and completing VAT returns.
of experience
coordinator is responsible for coordinating all clinical trial activities according to good clinical practice, areas:
Desirable
coordinator is responsible for coordinating all clinical trial activities according to good clinical practice, performance areas: Oversee all operations in the clinical trial to ensure protocol and GCP compliance Assist study and missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor, and regulatory regulatory authorities regarding notifiable trial events Prepare for and manage participant visits and work experience: 3-5 years experience in clinical trials/research Desirable additional education, work experience
coordinator is responsible for coordinating all clinical trial activities according to good clinical practice, performance areas: Oversee all operations in the clinical trial to ensure protocol and GCP compliance Assist study and missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor, and regulatory regulatory authorities regarding notifiable trial events Prepare for and manage participant visits and work experience: 3-5 years experience in clinical trials/research Desirable additional education, work experience