Job Details
We are growing and looking to add multiple Senior Clinical Research Coordinators to the TPS team.
The Senior Clinical Research Coordinator is tasked with the responsibility to conduct clinical trials according to the protocol, internal policies/procedures/best practices, and regulations governing clinical research in the USA. A CRC must be organized, efficient, and effective in order to maintain all the responsibilities of the position.
Key Responsibilities:
1. Serve as a primary coordinator for a specific study as assigned by management to conduct the following general study operations:
- Work under the direction of the internal management team
- Completely and accurately execute and document study visit procedures as required by the study protocol, internal policies/procedures/best practices, and regulatory requirements
- Conduct various required medical procedures and measurements as required by various protocol/s. These procedures/measurements may include one or more of the following: EKG (electrocardiograms), Holter Monitoring, PFT s (pulmonary function tests), Bodily Fluid Testing (urine screens, nasopharyngeal, saliva), Blood Draw, Blood Pressure, Pulse Rate, Oxygen Saturation, Weight, and Height.
- Coordinate visit schedules with all internal & external stakeholders such as, subjects, study doctors, external vendors, CRO/Sponsor staff, and other visit/study specific contributors
- Maintain regulatory documents and complete/report the required documents as required by study specific reporting schedules
- Establish the necessary knowledge and functional capability needed to be able to efficiently and effectively train site staff on the protocol & procedural requirements of studies for which they are the assigned lead CRC
2. Function as a supporting coordinator through collaboration with other CRCs and site staff to help complete the site work
3. Perform essential office tasks as required
Education & Work Experience Requirements:
1. Bachelor s degree in a scientific or healthcare field preferred
2. 1-2 years in clinical research experience preferred
Required Knowledge, Job-related Skills and Abilities:
1. Excellent written and verbal communication skills
2. Knowledge of medical terminology, clinical methods, procedures, and applications used in clinical trials
4. Demonstrable organization skills
5. Ability to stratify and manage multiple priorities
6. Ability to work independently, within a multi-disciplinary team, as well as with sponsors and vendors
7. Proficient in routine office procedures and tools including MS Office and other web-based platforms
Given our exciting and rapid growth, we offer the unique ability to progress in your career. With a proven internal career pathway that involves real mentorship and training, you are able to reach the future career you want to have.
If you are interested and fit the job requirements, we urge you to apply to learn more about TPS and the position. A member of our Talent Acquisition team will review your CV and then reach out at an appropriate time.