Senior Research Coordinator
4 weeks ago
Our culture and values guide how we work and treat one another. Cortica celebrates diversity and fosters an inclusive environment, seeking ideas and opinions from everyone on the team. We safeguard equal rights and respect for all individuals, regardless of race, color, religion, sex, national origin, age, disability, creed, genetic information, sexual orientation, gender identity or expression, ancestry, veteran status or other applicable, legally protected characteristics. All Cortica employment decisions are made based on an individual's qualifications and ability to successfully perform the job responsibilities.
What will you do?
- Independently perform all research tasks for on-site clinical trials.
- Seek out innovative solutions for process efficiency.
- Operate in a self-directed manner, with support from the global research coordinator and principal investigator as requested.
- Oversee training of the practical aspects of role for Research Assistants and Coordinators, mentorship of Research Assistants and Coordinators.
- Support the establishment of new trials.
- Hold responsibility for problem-solving and decision-making that directly impacts the experience of study participants, interpretation of the protocol, relationship with the Sponsor team, and general success of the Cortica Innovation Network.
- Responsible for effective and punctual communication with study Sponsors.
- Communicate with families and organizations throughout the community to spread awareness of research opportunities for local children and adolescents.
- Recruit, screen, schedule, enroll, and run participants both in-clinic and in-home.
- Work proactively to ensure the research performed fulfills all requirements of the applicable protocol and sponsor group.
- Take initiative to complete study tasks in a purposeful manner, looping supervisory staff and sponsor teams in when challenges arise.
- Maintain organized participant scheduling, internal calendars, participant data, and visit coordination.
- Master various research assessments, which may include ECGs, taking vitals, supporting with blood draws, running devices, and/or cognitive and behavioral assessments.
- Ensure secure and accurate data collection, entry, and record-keeping.
- Develop procedures to ensure all study materials are organized and stored to the appropriate degree for successful study conduct.
- Frequently travel around the community to provide accessibility to research for local families.
- Develop procedures to ensure all study materials are organized and stored to the appropriate degree for successful study conduct.
- Ensure secure and accurate data collection, entry, and record-keeping.
- Master various research assessments, which may include ECGs, taking vitals, supporting with blood draws, running devices, and/or cognitive and behavioral assessments.
- Maintain organized participant scheduling, internal calendars, participant data, and visit coordination.
- Take initiative to complete study tasks in a purposeful manner, looping supervisory staff and sponsor teams in when challenges arise.
- Work proactively to ensure the research performed fulfills all requirements of the applicable protocol and sponsor group.
- Recruit, screen, schedule, enroll, and run participants both in-clinic and in-home.
- Communicate with families and organizations throughout the community to spread awareness of research opportunities for local children and adolescents.
- Responsible for effective and punctual communication with study Sponsors.
- Hold responsibility for problem-solving and decision-making that directly impacts the experience of study participants, interpretation of the protocol, relationship with the Sponsor team, and general success of the Cortica Innovation Network.
- Support the establishment of new trials.
- Oversee training of the practical aspects of role for Research Assistants and Coordinators, mentorship of Research Assistants and Coordinators.
- Operate in a self-directed manner, with support from the global research coordinator and principal investigator as requested.
- Seek out innovative solutions for process efficiency.
- You hold a bachelor's degree in related field (Biology, Neurobiology, Neuroscience, Psychology, etc.).
- You have 2+ years of professional experience.
- You have 1+ years of clinical research experience.
- You have 2+ years of professional experience.
[Privacy Notice ]** For Individuals who reside and work in California** For driving roles: This position will require successfully completing a post-offer background check and motor vehicle report. Qualified candidates with criminal history and/or driving violations will be considered and are not automatically disqualified, consistent with applicable federal law, state law (the California Fair Chance Act), and local ordinances (San Francisco Fair Chance Ordinance, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County's Fair Chance Ordinance for Employers). For non-driving roles: This position will require successfully completing a post-offer background check. Qualified candidates with criminal history will be considered and are not automatically disqualified, consistent with applicable federal law, state law (the California Fair Chance Act), and local ordinances (San Francisco Fair Chance Ordinance, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County's Fair Chance Ordinance for Employers). Fair Chance Ordinance (Los Angeles, CA)Cortica
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