Laboratory Manager
$54k - $62kActalent
Schedule Internal | Permanent Full Time | Monday - Friday | 8:00 AM - 5:00 PM On-Site Required (no remote flexibility) Salary: $54,000 - $62,000 based on experience Bonus Potential: $2,000 annually (paid out mid‑year and year‑end) Monthly Cell Phone Allowance: $100 Job Summary The On‑Premise Manager (OPM) has multiple responsibilities. Primarily, the OPM is responsible for the fulfillment of all requisitions, ensuring client satisfaction through business activities and satisfaction of the contractors on site. The OPM will manage the contractor experience by providing world‑class customer service by managing communication proactively related to essential job functions. The OPM must have the ability to effectively communicate to contractors, potential contractors, client contacts and internal contacts. Essential Functions Perform all necessary contractor screenings to ensure their qualifications meet open positions (interviews, reference checks, skills testing, background checks, orientations, site tours, etc). Address contractor frequently asked questions pertaining to the assignment, pay, benefits, etc. Maintain and manage contractor workforce according to the client specific Progressive Discipline Program as outlined in the Aerotek @ Client Employee Handbook, including monitoring attendance & lateness, providing warnings, etc. Follow Injury Reporting Protocol by communicating with the appropriate internal contact and the local medical facility that provides post‑accident care. Serve as the interface between client managers, local office (if applicable) and contract employees, including regular attendance of client production and/or staff meetings. Maintain all documentation using Aerotek's online system and/or client systems to track performance feedback regarding contractors. Deliver performance feedback to on‑site contractor as needed. Deliver and maintain all client related requirements related to on‑site contractor workforce, such as route audits of contractor PPE and other employee compliance measures as client specifies. Maintain a professional work environment in alignment with current client culture, while maintaining the Aerotek expected standards of the guiding principles. Use Aerotek Employee Relations as escalation point and resource for employee issues. Utilize the available and appropriate resources of Aerotek Inc. for conflict resolution. Execute supervisory responsibilities in accordance with the organization’s policies and applicable laws. Responsibilities include interviewing, hiring, and training internal Aerotek employees; planning, assigning, and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems. Qualifications Preferred: Bachelor's Degree in Business or related field or prior business experience. Required: 1+ years of experience or more with any one or a combination of the following: high‑volume recruiting, managing a high‑volume account, or providing on‑premise support to a client. Equal Opportunity Employer Statement Actalent is an equal opportunity employer. We are committed to creating and fostering an inclusive environment for all employees. #J-18808-Ljbffr
$65 - $75 per hour
Position: PFAS Laboratory Manager Location: Raleigh, NC Pay: $65 to $75/hour (Depending on experience) Type: Full-time; Contract Schedule: Day Shift, 8:00am to 5:00pm Greene Resources is seeking a hands‑on PFAS Laboratory Manager to lead laboratory operations, supervise...SuggestedFull timeContract workDay shift- ...research activities in accordance with approved protocols administered by the College of Medicine (COM) Center for Clinical Research Management (CCRM) for the Department of Internal Medicine/ Division of Diabetes Endocrinology; assists with assessing patient records to...SuggestedShift workDay shift
$70k - $80k
...compliance with ALCOA‑C standards Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPs Manage subject recruitment, informed consent, and retention activities Ensure timely EDC data entry and resolution of queriesReport and...SuggestedFull timeLocal areaRemote workMonday to Friday$146.54k - $189.64k
...Coordinating and supervising all aspects of a clinical study, including monitoring clinical trial sites. Assisting the Clinical Program Manager in overall study management. Drafting and coordinating review of relevant documents such as protocols, informed consents, case...SuggestedContract workInterim roleLocal area- ...Responsibilities Demonstrated ability to manage CROs, vendors, study timelines, risks, action items, and cross-functional deliverables. Ability to identify issues, evaluate options, make sound recommendations, and drive timely resolution. Strong verbal, written, organizational...SuggestedWork at office
$125 - $135 per hour
...Our FSO team is seeking an Cell & Gene Therapy Clinical Project Manager to join our growing team. This role requires 2 + years of... ...a related allied health profession (i.e., nursing, medical or laboratory technology) from an appropriately accredited institution.Fortrea...Full timeContract workPart timeWork at officeLocal areaRemote workFlexible hoursNight shift- ...biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs). With close to 30 owned and managed research sites across the country, M3 Wake Research is one of the largest independent, multi-site clinical research companies in...Full timeFlexible hours
- ...1(k) retirement plan with company-match, and an annual incentive program. Summary: The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocity’s SOPs. Responsibilities Duties/Responsibilities: Conduct and...Work at officeFlexible hours
- Greene Resources is seeking a PFAS Laboratory Manager in Raleigh, NC to lead laboratory operations and supervise PFAS analysts. This is a hands-on position, requiring experience in analytical chemistry and PFAS analysis. The ideal candidate will have over 7 years of experience...
- ...company-match, and an annual incentive program. Summary: Subject matter expert and leader of a clinical trial team to conduct and manage clinical trial(s) from start up through study close out in accordance with the study protocol, GCP, and Velocity’s SOPs. Responsibilities...Work at officeFlexible hours
- ...Clinical Research Coordinator II (CRC II) is an experienced research professional who works collaboratively with clinical research site management and the Principal Investigator to support the successful execution of clinical trials. The CRC II independently manages day‑to‑...Flexible hours
- ...site/ Raleigh) Position Description: The Clinical Research Coordinator (CRC) works under the guidance of the clinical research site management and Principal Investigator (PI). The CRC manages, supports, facilitates and coordinates daily clinical trial activities, playing...Flexible hours
- ...Research Coordinator (CRC) is a specialized research professional working with and under the guidance of the clinical research site management and Principal Investigator (PI). While the PI is primarily responsible for the overall conduct of the clinical trial, the CRC...Flexible hours
$75k - $105k
...representatives, investigators, and Care Access Research personnel and management. Coordinate and attend pre‑study site visits, site initiation... ...such as blood draws, vital signs, ECGs, etc. Review laboratory results, ECGs, and other test results (e.g., MRIs) for completeness...Full timeTemporary workWork at officeLocal areaWorldwideVisa sponsorshipWork visaFlexible hours- A global midsize CRO is seeking a Senior Project Manager to oversee clinical trials from start-up to closeout. This role involves managing the technical, financial, and operational aspects of projects while ensuring deliverables meet customer expectations. The ideal candidate...Worldwide
- Worldwide Clinical Trials is seeking a Project Manager to lead global oncology trials from start‑up through closeout. You will coordinate multi‑office teams, oversee technical, financial, and operational aspects, and ensure deliverables meet time, quality, and cost expectations...Worldwide
- Syneos Health is looking for a Clinical Project Manager II to lead global oncology clinical trials. This remote role requires 3+ years of experience in Clinical Project Management, especially in oncology. The manager will oversee study execution, coordinate with stakeholders...Remote job
$75k - $105k
...representatives, investigators and Care Access Research personnel and management. Coordinate and attend pre-study site visits, site... ...procedures, such as blood draws, vital signs, ECGs, etc. Review laboratory results, ECGs, and other test results (e.g., MRIs) for...Full timeTemporary workWork at officeLocal areaWorldwideVisa sponsorshipWork visaFlexible hours$57 - $71.32 per hour
...Description Job Description Job Title: Contract Clinical Study Manager Job Description The Contract Clinical Study Manager... ..., site worksheets, vendor and site manuals, pharmacy manuals, laboratory manuals, monitoring plans, and monitoring reports, as applicable...Contract workTemporary workWork at officeRemote workMonday to FridayDay shift3 days per week$114k - $210.9k
...Experienced Clinical Trial Manager - Full-ServiceSyneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum,...Contract workFlexible hours$112k - $222k
Position Overview The Manager, Clinical Operations Site Management (Franchise Lead) is responsible for providing on‑time and quality delivery of site management services from assigned Clinical Trial Managers (CTMs) within assigned therapeutic area(s) and program(s). Responsibilities...Remote jobWorldwide- ...encompasses coordination of remote activities for clinical studies, where you will support communications, assist with screenings, and manage documentation compliant with regulations. The ideal candidate should possess a bachelor’s degree and relevant experience, ideally...Remote work
- ...position provides supervision for the department(s) of OhioHealth Laboratory Services. Responsibilities and Duties 30% Supervises and... ...associates in the department when needed or as determined by the manager. 5% Performs miscellaneous duties as assigned. As a High...Local areaShift workAfternoon shift
$120k - $135k
...Job Responsibilities As a Clinical Project Manager II, you will help drive the operational execution and delivery of global oncology... ...and issue resolution Oversee external vendors, CROs, central laboratories, imaging vendors, and specialty providers Coordinate Clinical...Work at officeRemote workFlexible hours- ...development to bring low-cost surfactant to the millions of premature babies with RDS born each year. What is the role? The Clinical Trial Manager (CTM) is responsible for managing various aspects of clinical trials including study start‑up, site management and monitoring...Interim roleWork at office
- ...Accentuate Staffing is partnering with an established biopharmaceutical organization who is hiring for a Laboratory Operations Manager. This is a direct hire opportunity with relocation assistance, working onsite. The ideal candidate is a collaborative and strategic leader...Relocation package
- ...strive for an environment in which inclusiveness drives productivity and results. Some responsibilities will include coordinating and managing multiple studies. They are also responsible for assisting the Principal Investigators and other clinical staff, with any study...Work at office
$49 - $59 per hour
Syneos Health, Inc. is seeking a Clinical Research Project Coordinator in Morrisville, NC to oversee various phases of clinical trials. Candidates must have a Registered Nurse or Bachelor's Degree and at least 1 year of clinical research experience. Responsibilities include...Hourly pay- ...A leading biopharmaceutical solutions organization in Morrisville, NC is seeking a Project Manager to support the management of clinical studies. The role involves coordinating study deliverables, managing vendor relationships, and developing risk mitigation strategies...
- Syneos Health is seeking a Project Manager - Future roles (US) to drive trial administration, financials and cross‑functional coordination across vendors. You will maintain the TMF plan, monitor study milestones, and support interim analyses and study closure. You will...Interim role
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