Celerion

Global CRO for early-phase development

Screening Conduct Specialist

Clinical Research OperationsPosted on Nov 11

Full-timeTempe, AZ, USA$18 /hrIn-person

About the Job

Requirements

A high school diploma or GED is required.
Strong reasoning and communication skills and attention to detail are required.
Bilingual English and Spanish language ability is preferred.
For sample-transport assignments, a valid Arizona driver's license in good standing is required.
For sample-transport assignments, completion of required CITI courses and Celerion SOP training on biological-sample transport and safe handling of hazardous materials is required.

Responsibilities

Perform screening and returns clinical duties, including check-ins, vital signs, ECGs, and blood draws, as assigned and when qualified.
Review medical history or other screening/returns data with participant candidates as needed.
Assist with participant outreach efforts.
Enter medical history or other screening data into study databases or other Celerion systems as needed.
Help ensure the safety of study and screening participants.
Assist the Principal Investigator or Sub-investigator with Spanish-language translation and procedures during physical exams as needed.
When assigned, transport biological samples and study data between sites; prepare samples for transport in compliance with Celerion SOPs and study protocols to ensure safe handling, sample viability, data integrity, and chain of custody.
Complete required transportation logs for sample and data tracking and upload them to Veeva daily.
Ensure biological samples and participant data from screening/returns clinics are delivered safely and on time.
Communicate to a supervisor any issues that could compromise sample or data integrity, viability, or chain of custody.
Follow local traffic laws and safe-driving standards while operating a Celerion vehicle.
Perform clinical conduct within study clinics, when qualified and assigned.
Help with laboratory rechecks and post-study rechecks as needed.
Contact subjects to schedule rechecks or missed events as needed.
Perform other reasonable duties as assigned.

Desired Qualifications

Post-high-school education or training in medical or life sciences is preferred.
CPR certification is preferred.

Salary Range: 18 to 18 (Currency: USD) (Pay period: per-hour-wage)

Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.

Celerion is seeking a Screening Conduct Specialist to support participant screening and returns procedures. In this role, you’ll perform essential clinical tasks including check-ins, vital signs, ECGs, phlebotomy, and medical history reviews. You may also assist with participant outreach, entering medical history in study databases, and assisting teams with screening and study procedures.

Qualified candidates will ensure participant safety, maintain data integrity, and support biological sample transport between sites in accordance with Celerion SOPs. The role requires strong communication skills, attention to detail, and adherence to all safety and regulatory standards.

Essential Functions

Perform Screening/Returns clinical duties
Qualified to perform all required Screening/returns clinical conduct tasks (check-ins, vital signs, ECGs, draw blood, etc) as assigned.
May review medical history or other Screening/returns data with participant candidates
May assist in participant outreach efforts
May enter medical history or other Screening data into study databases or other Celerion systems
May be responsible for safety of study/screening participants
May assist Principal Investigator/Sub investigator with Spanish language translation and procedures during physical exams
Transport biological samples/study data between sites, when assigned:
Prepare biological samples for transport, in compliance with Celerion SOPs and study protocols, to ensure safe handling, sample viability/data integrity and chain of custody.
Complete required transportation logs for proper sample/data tracking and upload to Veeva on a daily basis.
Ensure biological samples and participant data from Screening/returns clinics are delivered in a timely and safe manner.
Communicate to supervisor any issues which may have the potential to compromise sample/data integrity, viability or chain of custody.
Must follow all local traffic laws and safe driving standards while operating a Celerion vehicle, and possess a valid AZ driver’s license in good standing

Other duties

May perform clinical conduct within the study clinics, as task qualified and assigned
May help with lab rechecks and post-study rechecks
May reach out to subjects to schedule rechecks or missed events
Conduct other reasonable duties as assigned

Knowledge/Skills/Education/Licenses**

High school diploma or GED
Post-high school education or training in medical/life sciences preferred
CPR certification preferred
Strong reasoning and communication skills and attention to detail
Bilingual English Spanish language ability preferred
For Sample Transport assignment:
Must have valid AZ drivers license in good standing
Must have completed required CITI courses and Celerion SOP training on the transport of biological samples and the safe-handling of hazardous materials.

Celerion Values: Integrity Trust Teamwork Respect

Are you ready to join our team?

Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.

Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as "Not Junk" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.

About the Company

Celerion

Global CRO for early-phase development

Celerion is a global contract research organization focused on early-phase drug development. It conducts contracted research across clinical trial design, feasibility studies, project management, clinical and medical monitoring, bioanalytical sciences, and regulatory affairs, using High Resolution Mass Spectrometry-based metabolite profiling to inform decisions. Its advantage comes from over 40 years of experience, specialized metabolite profiling, and a global, integrated service model that accelerates development timelines. The goal is to help pharmaceutical and biotech clients bring safe and effective treatments to patients faster through rigorous, high-quality research.

Company size: 1,001-5,000
Company stage: Acquired
Total funding: Not listed
Headquarters: Lincoln, NE
Founded: 2010

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