Clinical Research Coordinator - Clinical Research

CenExel; Los Alamitos (CA); Sur place; USD 62 000 - 75 000; Plein temps

Résumé du poste

CenExel Clinical Research in Los Alamitos, CA is seeking an experienced Clinical Research Coordinator to coordinate clinical trials in accordance with ICH/GCP, protocol and company guidelines. You will support patient involvement from initiation through completion and manage data collection and reporting.

The role requires 1+ year of CRC experience, knowledge of federal human subjects protections, strong communication and teamwork, and the ability to work both independently and within a study

Qualifications

• Minimum 1+ years of Clinical Research Coordinator experience.
• Knowledge of Federal regulations protecting human subjects in research (ICH/GCP).
• Strong leadership and mentorship skills.
• Developing and maintaining effective working relationships with team, sponsor, and vendors.
• Excellent verbal and written communication; ability to work independently or in a team.

Responsabilités

• Coordinate all aspects of patient involvement from study initiation to completion.
• Organize research information for clinical trials.
• Observe subjects and assist with data analysis and reporting.
• Schedule data collection and ensure timely capture.
• Document adverse events and protocol deviations.
• Report research data to maintain quality and compliance.
• Perform administrative and regulatory duties related to the study.
• Participate in protocol development activities.
• Ensure site receives accurate information and supplies from sponsors.
• Educate participants and caregivers on protocol specifics and expectations.
• Perform safety and efficacy assessments per protocol.

Connaissances

CR Coordinator

Leadership

Mentorship

Regulatory knowledge

Communication

Crisis management

Teamwork

Formation

Bachelor's Degree

High school diploma or equivalent

Description du poste

About Us

Each of CenExel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.

Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.

Schedule

Monday - Friday (08:00 am - 4:30 pm)

Salary Range

$62,000 - $75,000 / Annually (Depending on education, experience, and skillset)

Job Summary

Responsible for assisting with coordinating clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies.

Essential Responsibilities And Duties

• Assists with coordinating all aspects of patient involvement from study initiation until study completion.
• Organizes research information for clinical trials.
• Observes subjects and assists with data analysis and reporting.
• Schedules the collection of data.
• Documents adverse events, protocol deviations, and other unanticipated problems appropriately.
• Reports research data to maintain quality and compliance.
• Performs administrative and regulatory duties related to the study as appropriate.
• Participates in other protocol development activities.
• Ensures site receives accurate information and supplies from sponsors (i.e.: source, protocol, scales, supplies, approvals, contacts, etc.)
• Educates potential participants and caregivers on protocol specific details and expectations.
• Performs safety and efficacy assessments per protocol (vital signs, EKGs, blood draws and other assessments as assigned).
• Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

Education/Experience/Skills

• High school graduate or equivalent; Bachelor's Degree, preferred.
• 1+ years of experience as a Clinical Research Coordinator (Required)
• Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials.
• Strong leadership and mentorship skills.
• Developing and maintaining effective working relationships at all levels of the organization, along with those at the sponsor and vendor level.
• Crisis management and problem-solving skills; ability to react calmly and effectively in emergent situations.
• Works independently as well as functioning as part of a team.
• Must be able to effectively communicate verbally and in writing.

Working Conditions

• Indoor, Office environment.
• Shift work, depending on location.
• Essential physical requirements include sitting, typing, standing, and walking.
• Lightly active position, occasional lifting of up to 20 pounds. Rarely lift over 20 pounds.
• Reporting to work, as scheduled, is essential.
• Overnight travel may be required for training and/or investigative meetings.

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.