Clinical Project Manager I
$60k - $75kAzenta US, Inc.
## **Job Description**At Azenta, new ideas, new technologies and new ways of thinking are driving our future. Our customer-focused culture encourages employees to embrace innovation and challenge the status quo with novel thinking and collaborative work relationships.Azenta Life Sciences is a global leader in the life sciences space with headquarters with offices and operations worldwide. We are a market leader in automated bio sample management solutions and genomic services across areas such as drug development, clinical and advanced cell therapies for the industry's top pharmaceutical, biotech, academic and healthcare institutions globally. We provide unparalleled capabilities with our lab analysis, sample management and storage services, informatics software, and consumables, with the largest installed base managing over 1 billion samples globally.**How You’ll Add Value:**The Project Manager I within the Program Management Organization (PMO) is expected to provide project management support to internal team members, as well as customers, to deliver Azenta Life Sciences solutions (Long Term Sample Management, Active Clinical Trial Sample Management, Regulated Products (GMP/GTP) Management) to clients, partners, and alliances. Under guidance from the Director, Clinical Program Management or Program Manager, the Project Manager I is expected to gain an in-depth understanding of the key clients and become an expert in Azenta Life Sciences services.**What You’ll Do:*** Serve as the primary client contact for assigned projects and establish working relationships with client project teams which result in client satisfaction, operational excellence and thereby increase potential for repeat business* Ensure that all customer expectations are documented and acted upon in compliance with regulatory requirements* Able to act efficiently in an environment with dynamic timelines and priorities. Accountable for the monitoring and reporting of performance metrics* Create required project plans* Implement and monitor progress against project plans and revise as necessary* Monitor project schedule and scope to ensure both remain on track* Project support may include kit provision and logistics, sample management, lab services support, relocation services, training, management, or support of alliances/ partnerships* Proactively engage in both quality assurance and risk management activities to ensure project deliverables are met according to both Azenta Life Sciences and client requirements* Participate in pre-sale discussions and client meetings as required* Actively participate in Azenta Life Sciences development through continuous improvement initiatives, contributing to Azenta’s culture of quality and productivity initiatives including the development of new processes and SOPs, and the maintenance of SOPs to maintain audit-ready alignment with the Azenta Business System* Mentor Client Coordinator as needed. Managing queries and resolutions**What You Will Bring:*** Associate’s or Bachelor’s degree in science or related field with a minimum of 2 year of experience in a regulated industry environment* OR High School Diploma plus a minimum of 5 years of experience in a regulated industry environment* Strong organizational skills and attention to detail* Excellent verbal and written communication skills; presentation skills, ability to engage in effective problem-solving conversations* Demonstrated ability to complete long-range projects as assigned* Demonstrated ability to prioritize work, customers, internal and external demands**Your Working Conditions:*** General office setting* The Employee may occasionally work in an area with potentially infectious materials* The Employee will be responsible for maintaining a clean work environment and enforcing and following Universal Precautions for bloodborne pathogens when working in an area considered to be potentially contaminatedJoin us and help enable life‐changing discoveries by keeping critical life science systems running reliably—every day.#IND123### If any applicant is unable to complete an application or respond to a job opening because of a disability, please email at View email address on click.appcast.io for assistance.**Azenta is an Equal Opportunity Employer. This company considers candidates regardless of race, color, age, religion, gender, sexual orientation, gender identity, national origin, disability or veteran status.**United States Base Compensation: $60,000.00 - $75,000.00The posted pay range for this position is an estimate based on current market data and internal pay structure. Final compensation may vary above or below this range depending on factors such as experience, education (including licensure and certifications), qualifications, performance, and geographic location, among other relevant business or organizational needs. #J-18808-Ljbffr
- ## Senior Clinical Project ManagerApply: US - Remote: Full time: Posted Yesterday: JR-0000008593\\*\\*Remote in the Northeastern US\\*\\*Pay... ...making process.**Role Overview:**The Senior Clinical Project Manager (Sr CPM) will be responsible for the overall execution of...SuggestedFull timeContract workFor contractorsLocal areaRemote work
- ...Clinical Research Coordinator Location: Tucker, Ga Job Type: Full-time This is an onsite position in Tucker, Georgia About... ...and supporting site operations. You will have the opportunity to manage your studies with a high degree of autonomy while working...SuggestedFull timeWork at office
- ...integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology,... ...clinical research organizations (CROs). With close to 30 owned and managed research sites across the country, M3 Wake Research is one of the...SuggestedFlexible hours
- ...The primary responsibility of the Clinical Research Coordinator III is to coordinate and conduct all aspects of a clinical study, with minimal supervision from the investigators. The Clinical Research Coordinator III is required to have an in-depth knowledge of protocol...SuggestedFull timeWork experience placementWork at officeLocal area
- ...About Absci Absci is a clinical-stage biotechnology company advancing novel therapeutics using generative AI. Our Integrated Drug Creation... ..., and YouTube. We are seeking an experienced Clinical Trial Manager to independently lead the end-to-end operational execution of...SuggestedContract workVisa sponsorshipWork visa
- ...Principal Investigator (PI) or designee, the Clinical Research Coordinator is responsible for... ...and aspects of collection and management of data for research protocols related to... ...status reports related to assigned research projects Participate in the design, development...Work at officeLocal area
$65k - $101k
...support and guidance to faculty and staff, managing initiatives that foster university... ...through large, complex multidisciplinary projects. Responsibilities include overseeing study... ...and compliance. The coordinator manages clinical trials, collaborates with various stakeholders...Full timeWork at officeWork from homeMonday to FridayFlexible hours- ...Monday-Friday 8am-4:30pm Hybrid remote Summary: The Clinical Research Coordinator I (CRC I) is a specialized research professional... ...according to protocol. # Utilizes the Clinical Trial Management System (CTMS) and adheres to protocol specific budgets. # Occasional...Full timeWork at officeLocal areaRemote workMonday to Friday
- ...Principal Investigator (PI) or designee, the Clinical Research Coordinator II is responsible... ...and aspects of collection and management of data for complex research protocols related... ...RC II will receive hands‑on training in project management, data management, and study procedures...Local area
$110.7k - $200.9k
...Location: Remote, United States Category: Clinical Trial Services Division: Precision... ...PM on monthly invoicing and variance management of clinical budget Develop study related... ...GCP audits Work closely with PM for project-specific resourcing issues Escalate...Contract workWork experience placementWork at officeLocal areaRemote workFlexible hoursNight shift- ...Kaiser Permanente in Los Angeles is seeking a data-driven professional to collect data for clinical trials independently and prepare study documentation for regulatory review, including IRB submissions. You will support clinical research activities and lab operations...
- ## Clinical Research Coordinator - Part TimeApply: Philadelphia, PA: Part time: Posted Today... ...of clinical trials (including database management, biological specimen processing, and... ...manage multiple concurrent objectives, projects, groups, or activities, making effective...Daily paidFull timeTemporary workPart timeFlexible hoursShift work
- ...Capital Health is seeking a seasoned nursing educator to lead clinical staff development and research education across the organization. The role emphasizes mentoring, evidence-based practice, and facilitating educational opportunities for nurses and graduate students...
- ...Emory University is seeking a Clinical Researcher to manage significant aspects of trials, supervise staff, and oversee data management. The role involves direct interaction with participants, protocol navigation, and compliance oversight in a busy research environment...
- ...Ann & Robert H. Lurie Children's Hospital of Chicago is seeking a clinical research coordinator to coordinate all clinical research activities with minimal supervision. You will manage start-up, site visits, regulatory compliance, data handling, and subject engagement...
$36.31 - $58.41 per hour
...Openings: 2 Work Schedule: 8 hrs/day, Monday-Friday #141770 Assistant Clinical Research Coordinator Filing Deadline: Wed 10/14/2026 This is a... .... DESCRIPTION In conjunction with and under supervision of the manager, incumbent will coordinate and assist with start-up procedures,...Hourly payContract workLocal areaMonday to Friday$30.74 - $49.46 per hour
...Description The Assistant Clinical Research Coordinator (ACRC) contributes to the overall operational management of clinical research/trial/study activities from design, set... ...and performs necessary tasks to coordinate projects and prioritizes work to meet necessary deadlines...Hourly pay- ...identifying the mechanistic targets for medical interventions through clinical research. We are committed to translational research, which... ...and detail-oriented Associate Clinical Research Coordinator to manage study operations from initial recruitment through study close-...
- ...Incumbent must be flexible and have reliable transportation to work in the different All of Us clinic locations around Orange County. Incumbent will be working on a 2-year project that involves enrollment of new participants and follow up of existing participants....Work at officeLocal areaFlexible hours
- ## Clinical Research CoordinatorApply: On Site: Purchase, New York, United States of America... ...studies, including the collection and management of clinical trial data. This role... ...reporting.· Collaborate with investigators, project managers, clinical management, and other...Permanent employmentFull timeInterim roleWork visaFlexible hours
- We are seeking a highly organized and motivated Clinical Research Coordinator (CRC) to join our research team. The CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance...Work at office
- Velocity Clinical Research is an owned and integrated research site organization, providing... ...Research Coordinator II conducts and manages multiple clinical trials from start up through... ...providing all close out reports. Apply project management concepts to manage risk and...Work at officeFlexible hours
- ...patient’s needs and type of cancer; innovative therapies and clinical trials; comprehensive patient and family support services;... ...with the conduct of clinical trials. KEY RESPONSIBILITIES: Manages research project databases, develops flow sheets and other study related...
- ...Aerogen Pharma: Aerogen Pharma is a US based clinical-stage specialty pharmaceutical company... .... What is the role? The Clinical Trial Manager (CTM) is responsible for managing... ...leadership, effective communication and project management skills, as well as a deep understanding...Interim roleWork at office
- ...Center is seeking a detail-oriented Research Coordinator to assist in coordinating patient participation and data collection for clinical studies in a supportive academic setting. You will handle regulatory documentation, IRB submissions, and scheduling, while ensuring...
- ## Clinical Research Coordinator II - Pulmonary & Critical Care MedicineApply: On Campus/... ...investigators from other divisions; responsible for managing and recording all phases of study... ...in developing plans for research projects and discusses the interpretation of results...Full timeWork experience placementWork at office
$20.16 - $29.01 per hour
...means to be part of Mass General Brigham. Job Summary The Clinical Research Associate/Clinical Research Coordinator I (CRA/CRC I)... ...to enroll eligible patients to clinical research protocols and manage all aspects of data collection and submission for multiple cancer...Hourly payRemote workShift work$66.27k - $107.1k
...Clinical Research Nurse Coordinator - Duke Cancer Institute Work Arrangement: On-Site Requisition Number: 274058 Regular or Temporary... ...therapies. You will also collaborate with sponsors, manage study operations, and contribute to the development of new research...Temporary workWork experience placementWorldwide- ...responsibility for critical coordination and management of the complex decisions and regulatory... ...Outcomes Research Institute ( PCORI ) projects, and investigator-initiated studies of... ...Experience: Experience in Phase I- III clinical research Preferred License: Preferred License...Full timeTemporary workWork at officeRemote work
- ...clinician-scientist, or clinician-educator track, depending upon proven experience, interest, and expertise in chemical pathology or clinical chemistry. The individual occupying this position will function in the Pathology Division of the Department of Pathology/OU Health...Full time
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