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Assistant Clinical Research Coordinator
Job in
San Francisco, San Francisco County, California, 94103, USA
Listed on 2026-10-10
Listing for:
Actalent
Full Time
position Listed on 2026-10-10
Job specializations:
-
Research/Development
Clinical Research, Research Assistant/Associate -
Healthcare
Clinical Research
Job Description & How to Apply Below
Assistant Clinical Research Coordinator Pulmonary Studies
Job Description
The Assistant Clinical Research Coordinator will support pulmonary clinical research studies in an academic research environment, with a strong focus on asthma biomarker research and airway disease. This role centers on patient-facing activities, including identification, recruitment, scheduling, informed consent, research visits, and longitudinal follow-up across multiple investigator-initiated and federally sponsored biobanking studies. The position offers hands-on exposure to multiple protocols, close collaboration with physicians and research staff, and a clear pathway for growth into a Clinical Research Coordinator role.
Responsibilities
+ Review electronic health records and upcoming pulmonary clinic schedules to identify patients who may meet eligibility criteria for multiple research protocols.
+ Pre-screen and triage potential participants for several concurrent studies, ensuring they meet inclusion and exclusion criteria.
+ Coordinate and run study visits, including obtaining informed consent, administering questionnaires, and supporting procedures such as blood draws and sputum induction in collaboration with clinical staff.
+ Schedule research visits and follow-up appointments, ensuring efficient use of clinic time and alignment with study timelines.
+ Manage ongoing patient communication, including outreach, reminders, and follow-up to support longitudinal participation and retention.
+ Collaborate closely with principal investigators, study physicians, and research staff to support efficient recruitment and study execution.
+ Digest and interpret study protocols to ensure that all study activities comply with protocol requirements and regulatory expectations.
+ Assist in organizing and maintaining study documentation and records related to patient screening, enrollment, and follow-up for multiple concurrent studies.
+ Adapt to fluctuations in patient volume and study workload, adjusting priorities to meet changing operational and investigator needs.
+ Contribute to a collaborative research environment focused on biomarker discovery, biologic treatment effects, and the development of screening tests to distinguish asthma subtypes.
Essential Skills
+
Experience with chart review and screening of electronic health records (EHR) for research eligibility.
+ Hands-on experience in clinical research or clinical trial support, particularly in patient-facing roles.
+ Demonstrated ability in patient recruitment, including pre-screening and triaging eligible participants for multiple studies.
+ Ability to coordinate and support study visits, including informed consent, administration of questionnaires, and assistance with procedures such as blood draws and sputum induction.
+ Strong organizational skills with the ability to manage multiple studies and shifting priorities simultaneously.
+ Flexibility to adapt to variable patient volumes, evolving study timelines, and differing investigator preferences.
+ Self-directed work style with the ability to act as a self-starter and work independently while maintaining accountability.
+ Problem-solving mindset, with the ability to address logistical and operational challenges in a research setting.
+ Capacity to quickly digest and understand complex research protocols and apply them accurately to daily workflows.
+ Excellent communication skills for effective interaction with patients, physicians, principal investigators, and research staff.
Additional
Skills & Qualifications
+ Interest in pulmonary research, particularly in asthma biomarkers, biologic treatments, and airway disease.
+ Experience or familiarity with investigator-initiated studies and federally sponsored biobanking repositories.
+ Motivation to develop a long-term career in clinical research, with interest in progressing from an Assistant Clinical Research Coordinator role to a Clinical Research Coordinator position.
+ Comfort working within a collaborative academic research environment with multiple ongoing studies.
+ Attention to detail and reliability in managing patient interactions, scheduling, and protocol adherence.
Work Environment
The role is based primarily onsite within an academic pulmonary research setting, working closely with a collaborative team of physicians, principal investigators, and research staff. The position supports multiple investigator-initiated and federally sponsored biobanking studies rather than traditional…
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