The growing team at the CTU is comprised of a Director of Clinical Trials Operations, Clinical Site Manager, Clinical Trial Associate, and Licensed Clinical Nurses with strong experience in clinical trials. Active private practice with patients available for clinical research or access to patients w...
Conducts clinical studies according to FDA regulations and guidelines. Protects the safety and welfare of the study subjects by ensuring that the study is conducted properly and in compliance with ICH/GCP and Optimal Research Standing Operating Procedures. ...
As a clinical research associate, you will lead and participate in the development of study designs, review and write protocols, prepare clinical trial agreements and lead the collection of the data and study findings. Senior Clinical Research Associate. Participate in the development of study-relat...
Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. Have a minimum of 3 years’ experience in monitoring pharmaceutical industry clinical trials. Have an in-depth knowledge of Good Clinical Practice, ICH g...
Apsida Life Science have partnered with a leading CRO who are looking for a CRC (Clinical Research Coordinator). ...
Clinical Research Nurse/CmedPosition Number: S-3209Type of Recruitment: ExternalPosition Summary:This position is comprised of both clinical responsibilities and regulatory responsibilities. Clinical responsibilities may include assisting with developing and implementing the activities of a clinical...
Come be a part of the Amway family! Job title:Senior Research Scientist - Nutrition Research & Clinical Investigator Department / Division:Core Nutrition / Innovation & Science Salary Grade:EXC 16 Salary Range:$107,914 - $139,653 per year, plus annual bonus Location:Ada, MI What do we need: We are l...
Alcanza Clinical Research (“Alcanza”) is a national, collaborative network of clinical research sites, founded on the mission to accelerate the development of new therapies by reducing barriers to clinical research participation for all. The RA performs clinical, lab, and administrative tasks as nee...
The Clinical Research Coordinator manages clinical trials conducted through the Clinical Protocol & Data Management Office. The Clinical Research Coordinator manages clinical trials (including some regulatory and budget requirements) and assists in the coordination of tests/visits for patients, work...
As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Activities include qualifying potential investigative sites, initiating clinical trials, maintaining study files, and providing instructio...
The Clinical Research Assistant will at times also act as a liaison with the radiation oncology clinic and medical oncology clinics when clinical trials are shared between departments and be the point person for providers and coordinators to reach out to for the clinical trial contacts. The Clinical...
The Clinical Research Coordinator will manage all clinical trial activities under supervision in compliance with all applicable laws, regulations, and procedures of study protocol while maintaining company mission, vision and values. Profound enables community physicians to offer clinical research a...
As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical ...
Utilize clinical and research knowledge to independently resect and obtain tissue from surgical specimens using sterile technique during cardiovascular surgeries at the Frankel Cardiovascular Center for clinical research purposes. The MI-AORTA Clinical Research Assistant will work within the Frankel...
As a CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Activities include qualifying potential investigative sites, initiating clinical trials, maintaining study files, and providing instructions to site personnel and...
The clinical research aide will perform a variety of research duties in support of funded studies related to maternal-child health. Early childhood/pregnant women research or clinical experience. The responsibilities for the position include: recruiting study participants, screening potential partic...
Part-Time Lecturer (Clinical Research Administration). Part-Time Lecturer (Clinical Research Administration). The School of Health Sciences is accepting applications for a part-time lecturer to teach specific Drug Development and/or Clinical Research Trial Management courses as assigned. Pharma/CRO/...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
Facilitate clinical testing and check results to determine patient eligibility for a clinical trial. Using established procedures, perform assessments independently and in collaboration with the physician investigator to ensure that the objectives of an established oncology research protocol are met...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
Certification is required through Association of Clinical Research Professionals (ACRP) as a Certified Clinical Research Coordinator (CCRC) or Society of Clinical Research Association (SOCRA) as a Certified Clinical Research Professionals (CCRP) or equivalent. Minimum 2 years of directly related exp...
POSITION PURPOSE Coordinate and participate in clinical research studies by performing activities involved in the collection, compilation, documentation of research data. The position will work with principal investigators and other research team members to accurately and efficiently carry out a ran...
Field monitoring of studies and data collection for clinical trials, assess all data documentation, reports, records, transcripts, exam results for consistency with case report form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to m...
The Innovation & Science Solutions team is a newly formed team focused on delivering efficacious science-based solutions with support for education and content.This team embraces the ambiguity of a new organization and consistently challenges our existing ways of working.Our team works closely with ...
Clinical responsibilities may include assisting with developing and implementing the activities of a clinical research trial which consists of selection of patients, treatment procedures, drawing blood, performing EKGs, recording adverse events, withdrawals, ethical/legal practices, monitoring and a...