As a Senior Clinical Research Associate, you will play a pivotal role in the success of our studies. Your site visits will be critical in ensuring compliance and excellence, while your innovative recruitment strategies will drive project outcomes.
To succeed in this role, you will need to possess excellent communication skills, both written and verbal. You should also have strong organizational and problem-solving abilities, as well as proficiency in Microsoft Office and relevant technology. In addition, you must have a minimum of 4 years of on-site monitoring experience, with preference for Oncology trial management exposure.
A key aspect of this role is the ability to empower sites with knowledge, providing essential training and maintaining robust communication channels. You will also be responsible for championing quality and integrity, evaluating and enhancing site practices to ensure adherence to protocols and regulations.
The successful candidate will be able to drive study progress, monitor every aspect of the study, from regulatory submissions to data query resolutions, ensuring seamless execution. They will also be required to maintain meticulous records and ensure all site documents are perfectly maintained.
This is an exciting opportunity to join a dynamic team and contribute to groundbreaking advancements in healthcare. If you are a motivated and organized individual with a passion for clinical research, we encourage you to apply.
* Essential Functions:
* Engage in Site Visits:Ensure the success of our studies through critical site visits.
* Recruitment Strategies:Develop and implement innovative plans to recruit study subjects.
* Empower Sites with Knowledge:Provide essential training and maintain robust communication channels.
* Champion Quality and Integrity:Evaluate and enhance site practices to ensure adherence to protocols and regulations.
* Drive Study Progress:Monitor every aspect of the study, ensuring seamless execution.
* Master Documentation:Maintain meticulous records and ensure all site documents are perfectly maintained.
* Collaborate and Innovate:Work closely with a passionate team to support project execution.
* Manage Finances with Precision:Oversee site financials and ensure timely invoice retrieval.
* Qualifications:
* Educational Excellence:A Bachelor's degree in a scientific or healthcare discipline is preferred.
* Experience Matters:At least 4 years of on-site monitoring experience, with preference for Oncology trial management exposure.
* Regulatory Savvy:Strong knowledge of GCP and ICH guidelines.
* Tech-Savvy:Proficiency in Microsoft Office and relevant technology.
* Communication Pro:Excellent written and verbal skills.
* Organized and Analytical:Strong organizational and problem-solving abilities.
* Time and Financial Management:Effective in managing time and finances.
* Team Player:Ability to build and maintain strong relationships with coworkers, managers, and clients.