Oncology CRA - East Coast
Apply NowCompany: Catalyst Clinical Research
Location: Sudbury, MA 01776
Description:
Job Description
Our Client is seeking an Oncology CRA on the East Coast with approximately 2-4 years of experience. This is not a senior level opportunity. This position is responsible for providing general, high-level clinical expertise to team members and research sites as needed, by performing field monitoring site visits during the course of a clinical study. S/he must have an understanding of site needs, and provide appropriate training for the sites. Plays a key role in maintaining site relationships. Must be willing and able to travel to research sites, as required. Complies with SOPs and all federal regulatory guidelines for Good Clinical Practice. Is committed to providing outstanding customer service to all customers, whether internal employees or external buyers, vendors or other individuals providing services. Essential Duties and Responsibilities (in order of importance): 1. Serves as a clinical research resource to all sites in an assigned geographic area. 2. Performs monitoring visits for multiple sites for clinical studies, including qualification/ pre-study, initiation, interim monitoring and close-out, as needed. 3. Compiles site performance metrics. 4. Supervises and facilitates the maintenance of records for each site, including all regulatory and study-specific files. 5. Provides superior customer service to both internal team employees and external customers by being congenial, having a positive attitude, and developing productive working relationships. 6. Provides clear, positive, and constructive communications (both written and verbal) to all members of the team and all external contacts. Position Qualifications: Strong interpersonal skills and excellent written and verbal communications skills. Expert knowledge of GCP's, ICH and FDA regulatory requirements; recent GCP training (within the last 12 months) required. Ability to function autonomously in a home-office environment and be highly organized Committed to quality oncology care in the context of clinical trials Ability to travel frequently to site locations (travel expectation -75%).
Experience Required
Education and/or Experience: Registered Nurse degree or BS in life sciences and oncology experience within a clinical research environment. Minimum of three years experience as a Clinical Research Associate, providing monitoring to oncology clinical trials. Clinical Research Certification, such as CCRA, preferred. Physical Requirements: Will have frequent traveling responsibilities in this position, with potentially 75% travel time Will work in a home office environment when not traveling
Our Client is seeking an Oncology CRA on the East Coast with approximately 2-4 years of experience. This is not a senior level opportunity. This position is responsible for providing general, high-level clinical expertise to team members and research sites as needed, by performing field monitoring site visits during the course of a clinical study. S/he must have an understanding of site needs, and provide appropriate training for the sites. Plays a key role in maintaining site relationships. Must be willing and able to travel to research sites, as required. Complies with SOPs and all federal regulatory guidelines for Good Clinical Practice. Is committed to providing outstanding customer service to all customers, whether internal employees or external buyers, vendors or other individuals providing services. Essential Duties and Responsibilities (in order of importance): 1. Serves as a clinical research resource to all sites in an assigned geographic area. 2. Performs monitoring visits for multiple sites for clinical studies, including qualification/ pre-study, initiation, interim monitoring and close-out, as needed. 3. Compiles site performance metrics. 4. Supervises and facilitates the maintenance of records for each site, including all regulatory and study-specific files. 5. Provides superior customer service to both internal team employees and external customers by being congenial, having a positive attitude, and developing productive working relationships. 6. Provides clear, positive, and constructive communications (both written and verbal) to all members of the team and all external contacts. Position Qualifications: Strong interpersonal skills and excellent written and verbal communications skills. Expert knowledge of GCP's, ICH and FDA regulatory requirements; recent GCP training (within the last 12 months) required. Ability to function autonomously in a home-office environment and be highly organized Committed to quality oncology care in the context of clinical trials Ability to travel frequently to site locations (travel expectation -75%).
Experience Required
Education and/or Experience: Registered Nurse degree or BS in life sciences and oncology experience within a clinical research environment. Minimum of three years experience as a Clinical Research Associate, providing monitoring to oncology clinical trials. Clinical Research Certification, such as CCRA, preferred. Physical Requirements: Will have frequent traveling responsibilities in this position, with potentially 75% travel time Will work in a home office environment when not traveling