Summary. The role of the. Clinical Study Coordinato. r is to ensure patient safety and wellbeing. The. Clinical Study Coordinato. r will coordinate and perform study visits under the guidance and supervision of the principal investigator. This is an office-based position, working in the same location as the principal investigator or in the designated clinic. To be successful in this role, the. Clinical Study Coordinato. r should be able to perfor...
Summary. . . . This is an exciting opportunity to work within a fast-paced, busy environment in the pharmaceutical, biotechnology, and medical device industries. As a Clinical Trial Assistant (CTA) you must assist the clinical research teams in ensuring the most effective and efficient conduct of clinical research studies by providing administration and project tracking support. . . Qualifications. . . To provide general administrative support to...
About the Role. The Clinical Research Unit (CRU) Director plays a pivotal role in overseeing the strategic direction and operational management of clinical research activities within the healthcare services sector. This position is responsible for ensuring that all clinical trials are conducted in compliance with regulatory standards and ethical guidelines, ultimately contributing to the advancement of medical knowledge and patient care. The CRU ...
About the Role. The Clinical Research Associate III will play a pivotal role in the management and oversight of clinical trials, ensuring that they are conducted in compliance with regulatory requirements and company standards. This position is responsible for monitoring study sites, collecting and analyzing data, and ensuring the integrity of the research process. The successful candidate will collaborate with cross-functional teams to facilitat...
Job Title: Administrative Assistant (AA). Department: Clinical Research. . Summary. The role of the Administrative Assistant is to support the CEO and the Project Management team in a well-organized and highly efficient manner. This is a full-time office-based position, working in a research clinic. The AA will be responsible for greeting patients, sponsors, and vendors, performing administrative duties, maintaining the overall cleanliness of th...
About the Role. We are seeking a highly motivated and detail-oriented Overnight Medical Assistant to join our team at Tranquil Clinical Research in Webster, TX. The successful candidate will be responsible for providing exceptional patient care and support to our medical staff during overnight shifts. As an Overnight Medical Assistant, you will play a critical role in ensuring the safety and well-being of our patients. You will be responsible for...
SUMMARY. Responsible for selling the Clinical Research services within the defined geographic location and collaborates with Business Development staff to ensure sales goals are achieved. The use of direct sales activities includes. prospecting, cold calling, in-person sales calls, proposal management, lead generation, and ultimately closing deals. Maintaining a high-activity sales effort that is documented and managed and provides timely reports...
Tranquil Clinical Research is enrolling clinical trials enrolling healthy human subjects. The following criteria must be met to apply. Between the ages of 18-45 years old. No current medical history. Healthy and free from clinically significant illness or disease, as determined by medical history, physical examination, clinical laboratory assessments, and other tests. No drug allergies. No peanut allergies. Not on any current medications or oral ...
Job Title: PRN. Research Nurse/Research Coordinator/Clinical Study Coordinator. overnight, weekend, and holiday staff **training is done during normal business hours. Department. Clinical Research. Reports to. CEO. Summary. The role of the study. Research Nurse. is to ensure patient safety and wellbeing. The. Research Nurse. will coordinate and perform study visits under the guidance and supervision of the principal investigator. This is an offic...
Summary. The role of this. Remote. Clinical Project Manager (CPM) is to ensure that the project is planned and conducted in accordance with relevant rules and regulations. The CPM will also need to ensure. overall success of the study trial, ensuring that the project is planned and conducted in accordance with all relevant rules and regulations, including the contract, company SOPs, ICH-GCP, FDA and other regulatory guidelines as applicable. The ...
Please do not call our office - we will reach out to you. Description. The Research Intern is an entry level clinical research position. The Intern will perform a variety of research, database and clerical duties of a routine and technical nature to support clinical trials and assist investigators to organize, gather and compile clinical research data. The Intern will primarily be responsible for the collection, aggregation, and analysis of data....
. Tranquil Clinical Research cares about the opinion of our employees and we want the world to know what an amazing place Tranquil is to work for. We always do the right thing, our number one job is the rights, safety and well being of our patients, we train hard and we play hard. We know that our employee provides an essential service and therefore we take better care of our employees than any CRO/Phase I unit in the US. Tranquil Clinical Resear...
