Clinical Research Coordinator

Actalent; San Francisco (CA); On-site; USD 45,000 - 47,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Time Off/Leave

Job summary

Actalent is seeking an Assistant Clinical Research Coordinator for pulmonary studies in San Francisco. This contract role focuses on asthma biomarker research and airway disease, with activities including patient identification, recruitment, scheduling, informed consent, and longitudinal follow-up across several protocols.

The role emphasizes hands-on exposure to multiple studies, collaboration with physicians and staff, and growth into a Clinical Research Coordinator position within an academic

Qualifications

• Experience screening electronic health records for eligibility.
• Hands-on clinical research support in patient-facing roles.
• Proven ability to recruit and screen participants for multiple studies.
• Coordinate visits, obtain informed consent, and assist with procedures.

Responsibilities

• Review EHRs and clinic schedules to identify eligible patients.
• Pre-screen and triage participants for multiple protocols.
• Coordinate study visits and assist with questionnaires and procedures.
• Schedule visits and follow-ups to align with study timelines.
• Maintain patient communication, reminders and retention.
• Collaborate with investigators and staff to support recruitment and execution.
• Ensure protocol compliance and proper study documentation.
• Adapt to varying study workloads and priorities.
• Support biomarker and airway disease research initiatives.

Skills

EHR screening

Clinical research support

Patient recruitment

Study visit coordination

Informed consent

Documentation management

Multi-study coordination

Communication

Job description

Job Title: 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 industry‑sponsored clinical trials, offering broad exposure to biomarker and airway‑disease research. Work hours may vary based on study visit schedules and patient volume, with some weeks busier than others. Limited remote flexibility may be available depending on study visit requirements, operational needs, individual performance, and leadership approval. The environment emphasizes professional attire appropriate for clinical and research interactions, as well as adherence to institutional policies and procedures while working with patients and clinical data.

Job Type & Location

This is a Contract position based out of San Francisco, CA.

Pay and Benefits

The pay range for this position is $33.31 - $34.68/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job‑related factors. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan Pre‑tax and Roth post‑tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long‑term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in San Francisco,CA.

Application Deadline

This position is anticipated to close on Oct 21, 2026. About Actalent

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [e-mail] for other accommodation options.

San Francisco Fair Chance Ordinance:

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector:

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):

We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.