Celerion

You'll lead a team of Consumer Research Coordinators in a clinical research setting, ensuring **on-time and defect-free execution** of research operations. You'll bridge communication between coordinators and the supervisor while managing staff development, scheduling, and compliance with protocols. This role combines **leadership responsibilities** with hands-on research management.

You'll generate and format Clinical Study Reports for a **contract research organization** using **MS Word** to client specifications. Your work directly supports faster drug delivery to market. This role offers exposure to the clinical research process.

You'll **review clinical source data** for a **clinical research organization**, ensuring completeness and accuracy for regulatory compliance. You'll perform **quality control checks** and data entry to support clinical trials.

You'll answer inbound calls from the public interested in clinical study participation, screening callers and recruiting eligible participants. You'll collect and enter medical history into our database and make outbound calls as needed. This role offers the chance to be part of a **highly experienced clinical pharmacology research network** dedicated to **accelerating drug development**.

You'll manage clinical laboratory operations and staff at our Belfast clinic, coordinating with site management to ensure timely, high-quality sample analysis. Your leadership will directly support **life-saving clinical research** and help bring **drugs to market faster**. This role offers the chance to work in a **well-established clinical pharmacology network**.

You'll join the Lincoln, NE clinical operations team as a **customer service concierge** for study participants, **managing their experience** from check-in to enrichment activities. Your work directly impacts participant satisfaction and helps get **drugs to market faster**.

You'll **perform scheduled events** according to study protocols and **work directly with study managers** to ensure trial success. You'll **monitor participant health** through vital signs, ECGs, blood draws, and telemetry.

You'll lead **clinical research projects** for a **CRO serving life-saving treatments**, ensuring deliverables and client satisfaction. Your core impact will be managing scope, timelines, and budgets while fostering **strong client relationships** through the full project lifecycle.

You'll **manage consumer research operations** at the Richmond Consumer Opinion Center, ensuring **compliance and quality** across all studies. Your core impact includes **staff oversight and client satisfaction**.

You'll work as a **Research Nurse** on overnight shifts conducting **clinical trials** with a healthy population. Your work supports the drug development process and impacts future healthcare.

You'll **assist with clinical research trials** working with a healthy population, performing **scheduled events per study protocol** and **identifying adverse events**. This role offers the ability to see the drug development process at work.

You'll manage clinical studies at our Lincoln, NE site, ensuring **compliance**, quality, and **profitability**. You'll oversee study execution from initiation to reporting, building client relationships and troubleshooting issues. Training is provided for this career-change opportunity.

You'll serve as a subject matter expert in **Veeva Clinical Data Management Suite (CDMS)**, handling eCRF design and EDC build programming for clinical trials. Your work will directly support life-saving treatments. This fully remote role offers the chance to impact global clinical data standards.

You'll monitor study participants and handle biological samples for a clinical research organization. You'll perform vital signs, ECGs, and phlebotomy to support drug trials. This role offers **comprehensive paid training** for both part-time and full-time shifts.

You'll oversee the conduct of clinical studies, ensuring compliance, quality, and profitability. You'll build client relationships, manage timelines, and solve problems to keep studies on track. **This role requires flexibility**, involving **evening and weekend work** during critical events.

You'll provide expert oversight of data management for **external site clinical trials**, ensuring data integrity and regulatory compliance. You'll serve as the primary Sponsor contact and coordinate cross-functional teams to deliver high-quality datasets on time.

You'll join our Dose Formulation team to **execute analytical tests** ensuring compounds meet specifications for clinical research trials. Core impact: you'll leverage analytical chemistry expertise to **ensure every dose is ready on schedule**. Required: Bachelor's in Chemistry/Biochemistry with 3-5 years of **analytical instrumentation experience**.

You'll **support daily laboratory operations** in a professional bioanalytical department. Your role ensures **data integrity and sample accuracy** through quality control reviews. This **part-time role offers flexible scheduling** ideal for students.

You'll monitor study participants, handle biological samples, and record data in a clinical research setting. You'll perform vital signs, EKGs, and phlebotomy while receiving **excellent training**. This role supports **life-saving drug development**.

You'll lead the **QA Bioanalytical team** and drive **QMS and process improvement initiatives** for a dynamic clinical research organization. Your work will ensure quality and compliance across studies, audits, and regulatory inspections, directly accelerating drug development.

You'll lead **ligand binding assay development** for a **CRO supporting clinical research**. You'll drive innovation in bioanalytical methods to accelerate drug development. This role offers the chance to author scientific manuscripts and present at conferences.

You'll join Celerion's Bioanalytical Services team in Lincoln, NE, processing biological samples using **chromatography** and **ligand-binding** techniques. Your work will directly support **clinical research** to accelerate drug development. This full-time role offers a starting salary of $20.50 per hour.

You'll serve as the primary on-site IT representative for our **Zurich site**, delivering comprehensive desktop and systems support. You'll be the trusted face of IT for Swiss colleagues, combining deep technical skills with **genuine service commitment**. This role offers the chance to work in a **regulated bioanalytical research environment**.

You'll join the Bioanalytical Division at Celerion, ensuring accurate sample management for clinical research. Your attention to detail will directly impact the speed of drug development. This entry-level role offers a consistent daytime schedule in a **nicotine-free, structured lab environment**.

You'll perform clinical procedures like vital signs, ECGs, and blood draws in a **clinical research setting** that helps bring drugs to market faster. You'll also **train clinical associates** on ECG and emergency procedures, and **identify and report adverse events** to medical staff.

You'll join a team of 10 colleagues at a clinical research site, managing participant screening and documentation. Your work will **help accelerate drug development** in a **swift, translational medicine environment**. This entry-level role offers a **springboard to professional growth** in clinical research.

You'll support pricing and proposal development for a **bioanalytical services team**, ensuring accurate budgets and financial tracking. Your work directly impacts **drug development timelines** and helps bring therapies to market faster. You'll collaborate across departments in a fast-paced CRO environment.

You'll join a **Clinical Pharmacology team** performing **pharmacokinetic data analysis** and **scientific interpretation** of study results. You'll interact with clients and contribute to regulatory submissions.

You'll coordinate consumer studies related to nicotine and tobacco products at Celerion. Primarily a **customer service-based role**, you'll manage participant activities including screening and evaluations. This part-time position offers **benefits** and requires flexibility for varied hours.

You'll coordinate global strategy and administration of bioanalytical systems like LIMS and ELN, partnering with stakeholders across US and Switzerland. Your work will drive **digital transformation** and **data integrity** in a regulated lab environment, directly impacting drug development speed. This role spans strategic leadership and hands-on system ownership.

You'll handle inbound calls from potential participants in **Phase 1 clinical drug trials**, screening for eligibility and scheduling appointments. This role ensures accurate data entry and supports study enrollment. Bilingual Spanish-English fluency is **required** for this hybrid position.

You'll coordinate global strategy and administration of **bioanalytical laboratory systems** and digital platforms, combining **strategic coordination with hands-on execution**. You'll ensure systems like LIMS and ELN are effectively implemented and compliant while enabling alignment between US and Switzerland labs.

You'll support **bioanalytical study scoping and pricing** for a **leading clinical research organization**. Your work directly enables accurate, competitive proposals that help get drugs to market faster. This role offers exposure to the full financial lifecycle of studies.