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<h3>Job Description</h3>
Description
Job Summary
\n
Serves as a key collaborator to investigators, providing clinical and behavioral research expertise. Participates in ongoing implementation science, quantitative and qualitative research, and pursues independent and collaborative research. Focuses on implementation science and also broadly contributes to a variety of activities including health outcomes, quality of life, and population health initiatives.
\n
Job Specific Duties
\n
<ul>\n
<li>Designs and conducts research studies, such as personalized medicine, quality of life, implementation science, and other priority areas.&nbsp; </li>
\n
<li>Collaborates with other investigators in developing and executing interdisciplinary clinical research.&nbsp; </li>
\n
<li>Provides consultation to investigators and project coordinators on clinical study design and development of research questions.&nbsp; </li>
\n
<li>Leads or supports the preparation of extramural grant applications and contracts.&nbsp; </li>
\n
<li>Analyzes and interprets complex data for reporting, presentations and publications.&nbsp; </li>
\n
<li>Contributes to high level discussions with funding agencies and research teams within organization and with collaborating organizations.&nbsp; </li>
\n
<li>Makes decisions for day-to-day operations of projects including the resolution of technical problems and questions from project staff.&nbsp; </li>
\n
<li>Monitors progress of study activities (e.g. data collection and validation, recruitment, pilot studies, focus groups, etc.) and ensures that study objectives are met. </li>
\n
<li>Collaborates with researchers, biostatisticians, data scientists, graduate students, residents and clinical fellows to ensure progress of studies.&nbsp; </li>
\n
<li>Oversees data collection and direct data analysis by staff.&nbsp; </li>
\n
<li>As a subject matter expert, trains and mentors researchers and trainees in scientific writing including grantsmanship and manuscript development.</li>
\n</ul>
Qualifications
Minimum Job Requirements
\n
<ul>\n
<li>Ph.D. in epidemiology or related field&nbsp; </li>
\n
<li>4-7 years of experience in a University or academic medical center environment </li>
\n
<li>2-4 years of work experience leading and contributing to multi-site research protocols, grant and manuscript writing, and implementing science initiatives</li>
\n</ul>
\n
Knowledge, Skills, and Abilities
\n
<ul>\n
<li>Experience in healthcare research setting to include management responsibility </li>
\n
<li>Experience coordinating, implementing and supervising live recruitment studies, including the preparation of clinical protocols and correspondence with the IRB, authoring consent forms, designing data collection tools and creating study tracking databases, preferred </li>
\n
<li>Knowledge of research principles, design and strategies, and data interpretation methods </li>
\n
<li>Able to work independently in accordance with established objectives </li>
\n
<li>Detail oriented, highly motivated, and committed to achieving excellence in the form of productivity and publications </li>
\n
<li>Able to negotiate and manage time commitments and resources </li>
\n
<li>Able to acquire and maintain knowledge of systems and databases </li>
\n
<li>Able to develop and present professional reports and presentations to senior-level audiences </li>
\n
<li>Able to develop and implement research instruments </li>
\n
<li>Ability to function in a team environment</li>
\n</ul>
 Job : Research Department : RI - ADMINISTRATION-2100-380950 Job Status :Full Time

Research Scientist - Neurology - Onsite (Full Time, Day shift)

<h3>Job Description</h3>
Job DescriptionDescription:
POSITION SUMMARY:
<ul>
<li>The Chief Medical Physicist is a board-certified specializing in therapeutic clinical services in external beam, including Adaptive-RT, SBRT, SRS, IMRT, VMAT, IGRT, SGRT, brachytherapy, and radiopharmaceutical programs. Your work will ensure the safe, accurate, and effective delivery of radiation therapy for our patients, making a direct impact on their care and outcomes.</li>
<li>At the Cancer Center of South Florida (CCSF), the Chief Medical Physicist plays a vital role within a collaborative, multidisciplinary team, requiring strong clinical and interpersonal skills to provide excellent clinical care, as well as a commitment to continuous learning and leadership within the field of radiation oncology.</li>
<li>In addition to fulfilling essential clinical responsibilities, the Chief Medical Physicist is expected to embody the shared values and professional standards that guide our organizational culture and partnership pathway.</li>
</ul>
 
CORE RESPONSIBILITIES:
Clinical Quality &amp; Efficiency
<ul>
<li>Oversee all technical aspects of radiation oncology services, including network treatment equipment, treatment planning systems, treatment delivery, and ancillary equipment.</li>
<li>Establish and implement specifications for acceptance testing, calibration, and performance of all radiation simulation, delivery, measurement, treatment planning, QA software, and related equipment. Ensure compliance with all relevant regulatory, professional, and accreditation standards.</li>
<li>Lead and participate in quality assurance (QA) programs in accordance with American Association of Physicists in Medicine (AAPM) guidelines, including monthly and annual equipment QA tests and weekly patient chart reviews.</li>
<li>Responsible for radiation protection programs and serve as Radiation Safety Officer (RSO) as required by departmental needs or contractual obligations.</li>
<li>Collaborate with TGH affiliates to implement physics and radiation quality management programs. Participate in the development, review, and approval of clinical procedures and attend departmental QA and leadership meetings.</li>
<li>Serve as the primary contact for leadership on matters of quality, safety, performance, and compliance related to the technical and safety aspects of radiation oncology.</li>
<li>Supervise physics and dosimetry staff, ensuring appropriate resource allocation and professional development.</li>
<li>Act as a certified radiation expert, providing guidance on equipment procurement, evaluation of new treatment technologies, regulatory compliance, and billing practices.</li>
<li>Manage registration and compliance for all ionizing radiation equipment and radioactive material licenses.</li>
<li>Ensure proper and timely maintenance of all radiation treatment equipment.</li>
<li>Coordinate the operational activities of the medical physics and dosimetry teams within the department.</li>
<li>Deliver high-quality, cost-effective physics support and treatment planning services.</li>
<li>Stay current with advancements in radiation oncology, emerging technologies, and best practices.</li>
<li>Demonstrate personal reliability and efficiency in handling treatment planning responsibilities.</li>
<li>Perform and verify treatment planning calculations and support accurate patient billing.</li>
<li>Complete all mandatory education, training, and department-specific competency requirements.</li>
<li>Adhere to departmental policies, including those related to attendance, punctuality, confidentiality, dress code, identification, and workplace safety.</li>
<li>Perform other duties as assigned.</li>
</ul>
 
 
Multidisciplinary Collaboration &amp; Collegiality
<ul>
<li>Collaborate with physicians, nurses, therapists, dosimetrists, physicists, pharmacists, and administrative staff to deliver coordinated, comprehensive care.</li>
<li>Participate in chart rounds, case reviews, care planning discussions, and quality, safety, and operations meetings.</li>
<li>Maintain respectful, supportive relationships with colleagues and contribute to a positive work culture.</li>
<li>Share professional insights in a constructive and collegial manner; resolve conflicts respectfully.</li>
</ul>
 
 
Proactivity &amp; Practice Engagement
<ul>
<li>Take initiative in solving clinical, operational, or organizational challenges.</li>
<li>Actively contributes to improving internal workflows, patient experience, and staff collaboration.</li>
<li>Engage in committee work, quality reviews, or special projects that enhance operations.</li>
</ul>
 
Patient Care Excellence &amp; Satisfaction
<ul>
<li>Create and implement personalized treatment plans tailored to each patient's needs based on the physician's directive.</li>
<li>Provide clear, compassionate communication and guidance with the clinical staff.</li>
<li>Maintain high patient and staff satisfaction through courtesy, respect, and service excellence.</li>
<li>Engage in ongoing communication with the clinical staff to promote trust and shared decision-making.</li>
</ul>
 
 
Regulatory &amp; Ethical Compliance
<ul>
<li>Comply with all federal and state healthcare laws, including HIPAA, FCA, AKS, and the Stark Law.</li>
<li>Follow CCSF’s internal policies, procedures, and ethical guidelines.</li>
<li>Maintain a valid, unrestricted medical license and promote a culture of compliance and accountability.</li>
</ul>
Requirements:
REQUIRED EDUCATION &amp; EXPERIENCE:
<ul>
<li>Master's or PhD degree in medical physics or related discipline.</li>
<li>Certified in therapeutic medical physics from the American Board of Radiology (ABR) or equivalent certification from the Canadian College of Physicists in Medicine (CCPM) or the American Board of Medical Physics (ABMP) required.</li>
<li>Ten years of work experience as a Medical Physicist in a full-service radiation therapy center</li>
<li>A minimum of 3 years of leadership experience or leading teams in a technical field.</li>
</ul>
 
REQUIRED KNOWLEDGE, SKILLS OR ABILITIES:
<ul>
<li>Knowledge of radiation oncology, diagnostics, and evidence-based radiation treatment protocols</li>
<li>Strong critical thinking and decision-making in complex medical planning situations.</li>
<li>Ability to clearly communicate with the care teams.</li>
<li>Ability to work in a multidisciplinary environment meanwhile promoting collegiality and mutual respect.</li>
<li>Ability to manage time and have a high attention to detail.</li>
<li>Ability to demonstrate leadership, integrity, and compliance with medical, ethical and legal standards.</li>
<li>Knowledge of Varian and GE equipment, use of electronic medical records, treatment planning systems, and QA software.</li>
</ul>

Chief Medical Physicist

<h3>Job Description</h3>
Job Description 
Job Summary 
Nammo Perry, Inc. is a U.S. defense contractor and a member of the Nammo Group (Nammo AS). Nammo Perry develops, manufactures and specializes in propulsion and energetic material products for tactical missiles, rocket motors, and warheads. Nammo Perry is presently expanding operations and is looking for dedicated team members to assist with new start-up operations and program execution. The Propellant Chemist will design, develop, and optimize solid propellant and adhesive bondliner formulations for rocket motors, ensuring high performance, safety, and reliability for aerospace applications. 
Responsibilities 
• Formulation Development: Design and develop solid propellant formulations, including oxidizers, binders, fuels, and additives, to meet performance, stability, and safety requirements
• Testing and Analysis: Conduct laboratory-scale mixing, casting, and curing of propellant formulations, followed by performance testing (e.g., burn rate, specific impulse, mechanical properties).
• Process Optimization: Optimize propellant manufacturing processes to ensure scalability, repeatability, and cost-effectiveness while maintaining quality standards.
• Safety and Compliance: Ensure formulations comply with safety, environmental, and regulatory standards. Conduct hazard assessments and implement safe handling procedures.
• Data Analysis: Analyze test data to evaluate propellant performance, stability, and aging characteristics. Provide recommendations for formulation improvements.
• Collaboration: Work closely with propulsion engineers and manufacturing teams to integrate propellant designs into rocket motor systems.
• Documentation: Prepare detailed technical reports, specifications, and standard operating procedures for propellant formulations and processes.
• Research and Innovation: Stay current with advancements in propellant chemistry and materials science. Propose innovative solutions to enhance performance and reduce costs.
Requirements, Education, and Skills
· MS or PhD strongly preferred in Chemistry, Chemical Engineering, Materials Science or related field with approximately five (5) years related work experience in energetics, adhesives or other chemistry field highly preferred.
· Knowledge of Microsoft Office software: Word, Excel, PowerPoint, Outlook and Visio, and web-based organizational filing systems. 
· Ability to utilize internal thermochemical analytical codes.
· Ability to understand relevant chemistries including elements of polymer, organic, physical and inorganic.
· Ability to understand and interpret physical and chemical properties data.
· Understanding of statistics related to Statistical Process Control (SPC).
· Strong presentation, organizational and interpersonal skills. Clear written and oral communication skills.
· Have demonstrated capability for independent work and creativity
· Ability to work within a cross functional team and a dynamic environment.
· High ethical standards of work and personal conduct.
· Ability and willingness to work outside of standard work hours when needed to resolve issues.
· Ability to obtain BATF approval to work with our products. 
· Ability to qualify for and, if necessary, obtain DoD security clearance.
• US Citizenship is REQUIRED.
· Work Location: Tallahassee, Florida with Travel to Perry, Florida as required
Training: 
· Year-Long Training Plan 
· Safety Orientation 
· HAZWOPPER Aware/Right to Know 
· Annual Drug and Alcohol Awareness 
· Annual Ethics Refresher 
· CUI and OPSEC 
 
This job description in no way states or implies that these are the only duties to be performed by the employee(s) incumbent in this position. Employees will be required to follow any other job- related instructions and to perform any other job-related duties requested by any person authorized to give instructions or assignments. All duties and responsibilities are essential functions and requirements and are subject to possible modification to reasonably accommodate individuals with disabilities. To perform this job successfully, the incumbent will possess the skills, aptitudes, and abilities to perform each duty proficiently. Some requirements may exclude individuals who pose a direct threat or significant risk to the health or safety of themselves or others. The requirements listed in this document are the minimum.

Propellant Chemist

<h3>Job Description</h3>
Job Description
Supports the enrollment of patients into clinical trials through recruitment, screening, enrollment and follow up of eligible subjects according to protocol requirements.
• Collaborates with the principal investigator to meet or exceed study enrollment.
• Reviews the study design and inclusion/exclusion criteria with physician and patient.
• Ensures the protection of study patients by verifying informed consent procedures and adheres to protocol requirements/compliance and provides close monitoring of subjects while on study.
• Ensures the integrity of the data submitted on Case Report Forms or other data collection tools by careful source document review. Monitors data for missing or inaccurate data and respond to queries.
• Creates study specific tools for source documentation when not provided by sponsor.
• Collects, completes, and enters data into study specific case report forms or electronic data capture systems.
• Generates and tracks drug shipments, device shipments and supplies as needed.
• Assists with sample collection to include environmental sample collection, packing and shipping of samples.
• Assists with study relevant forms required for various regulatory and oversight committees.
• Reports and follows up on serious adverse events as necessary.
• Implements study-specific communications.
• Maintains accurate and complete records including regulatory documents when applicable, signed informed consent forms, source documentation, drug dispensing logs, device utilization logs, subject logs and study-related communications.
• Tracks and reports adverse events, serious adverse events, protocol waivers, deviations, and violations.
• Attends study specific on site meetings, Investigator meetings, conference calls and monthly CRC meetings as required or asked to do so.
• Apprises principal investigator of all study specific medical issues for guidance.
• Assists Sponsor, VA, FDA, IRB and other audit teams as needed.
• Reviews and responds to any monitoring and auditing findings
• Maintains patient confidentiality according to ethical and legal requirements.
• Assists in providing coverage for other projects and investigators as necessary or when asked to do so.
• Practice and adhere to the "VA Rules of Behavior."
• Performs other related duties as assigned by management.
 SUPERVISORY RESPONSIBILITIES:
• This job has no supervisory responsibilities.
QUALIFICATIONS:
• Bachelor's Degree (BA) from four-year college or university, or four years of related experience and/or training, or equivalent combination of education and experience.
• Certificates, licenses and registrations preferred but not required:
o Specialty research certification such as ACRP’s CCRA, CCRC, ACRP-CP or SOCRA’s CCRP.
• Computer skills required: Microsoft Office Suite
• Other skills required:
o Working knowledge of medical and research terminology.
o Working knowledge of federal regulations for human subject protections and Good Clinical Practices (GCP).
o Ability to communicate and work effectively with a diverse team of professionals.
o Excellent organizational and prioritizing capabilities.
o Strong computer skills with demonstrated abilities using clinical trial database, electronic data capture.
o Excellent interpersonal skills, detailed oriented and meticulous.
o Excellent professional writing and communication skills.
o Ability to demonstrate proficient achievement of ‘Intermediate CRC’ based on ACRP Core.
o Specimen and/or tissue collection, handling &amp; processing.
o Phlebotomy experience
 Monday - Friday 7am - 4pm on-site 40 hours per week

Health Science Specialist

<h3>Job Description</h3>
Job Description
Window Measurement Specialist - Conduct measure calls for windows and doors.
Qualified Candidate MUST be capable of measuring windows and doors.
Required Skills: • Detailed Oriented and experienced multi-tasking • Exceptional communication skills-comfortable working with customers • Window and Door Installation experience
Experience: • 2+ years of window installation experience
Position Offers: • Competitive Compensation-Salary • Career Growth
To Apply: All applicants must submit their updated resume along with their contact phone number.
 #hc199559

Window Measurement Specialist

<h3>Job Description</h3>
Job DescriptionJoin Our Team as a Lab Supervisor - Emergency Department at Labcorp!
Are you an experienced clinical laboratory professional ready to take the next step in your career? If you thrive in a fast-paced environment and have a passion for leadership, we want to hear from you! At Labcorp, we are dedicated to our mission: "Improving Health, Improving Lives." Join us in Miami, FL, and be part of a team that makes a real difference every day.
$15,000 Sign-On Bonus for External Candidates!Why Choose Labcorp?
We offer a dynamic work environment where you can grow and thrive. Here’s what you can expect:
Work Schedule:
1st Shift, Monday - Friday, 8:00 AM - 4:30 PM, with occasional weekends as needed.
Benefits:
As a valued member of our team, you’ll enjoy comprehensive benefits, including:
<ul>
<li>Medical, Dental, and Vision coverage</li>
<li>Life Insurance and Short/Long-Term Disability</li>
<li>401(k) Plan with company match</li>
<li>Paid Time Off (PTO) or Flexible Time Off (FTO)</li>
<li>Tuition Reimbursement</li>
<li>Employee Stock Purchase Plan</li>
</ul>
Your Role and Responsibilities:
As the Lab Supervisor, you will:
<ul>
<li>Oversee daily operations of the Emergency Department lab</li>
<li>Ensure accurate and timely laboratory test results</li>
<li>Supervise, train, and mentor laboratory personnel</li>
<li>Monitor workflow and ensure adequate staffing</li>
<li>Resolve production errors and implement process improvements</li>
<li>Maintain compliance with state and federal regulations</li>
<li>Engage in quality control and assurance activities</li>
<li>Conduct regular coaching sessions with your team</li>
<li>Perform bench work as needed and maintain technical proficiency</li>
</ul>
What We’re Looking For:
To succeed in this role, you should have:
<ul>
<li>Associate’s degree in a Chemical or Biological science, Clinical Laboratory Science, or Medical Technology (Bachelor’s preferred)</li>
<li>A minimum of 4 years of experience as a Technologist</li>
<li>Previous supervisory or leadership experience is highly preferred</li>
<li>Florida Supervisor Generalist license</li>
<li>ASCP Certification (preferred)</li>
<li>Strong knowledge of CLIA, CAP, and relevant state regulations</li>
<li>Proficiency in Laboratory Information Systems and Microsoft Office</li>
<li>Excellent communication skills, both written and verbal</li>
<li>A keen eye for detail and strong organizational skills</li>
<li>The ability to adapt and make decisions in a changing environment</li>
</ul>
Working Conditions:
To ensure the safety of our patients, this position requires successful completion of medical surveillance testing as part of the onboarding process. Labcorp is committed to providing reasonable accommodations for those who need them.
Ready to Make a Difference?
If you're looking for a career that offers growth, continual development, and the chance to make a real impact, apply today!
Labcorp is Proud to be an Equal Opportunity Employer
We strive for inclusion and belonging in our workforce and do not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual.
Keywords:
clinical laboratory supervision, laboratory operations, emergency department lab, quality control, staff training and mentoring, CLIA compliance, laboratory information systems, medical technology, process improvement, laboratory testing

Lab Supervisor - Emergency Department

<h3>Job Description</h3>
Job Description
LOCATION: Robert Boissoneault Oncology Institute, Lecanto/Crystal River, Florida
The Robert Boissoneault Oncology Institute (RBOI) is a physician owned private practice and is recruiting a Board Certified Physicist to join our staff of eight physicians, five physicists, seven dosimetrists, two dedicated in-house linear accelerator engineers, and 3 in-house IT professionals. The position available is for our Lecanto location due to the upcoming retirement of our current physicist who has worked at that location for 20 years.
RBOI has four ACR (American College of Radiology) accredited radiation therapy facilities equipped with 8 Varian linear accelerators, 4 Philips large-bore 16 slice CT scanners, and one Nucletron Flexitron HDR treatment unit. All treatment planning is currently performed in Varian Eclipse coupled with a full Radformation package. Image fusion is performed via MimVista. R&amp;V is Citrix cloud based Mosaiq. RBOI uses a full array of SunNuclear QA products as well as the OmniPro water tank scanning system. All four facilities work in unison via a unified database and a standard set of procedures. Patient load is typically 40-60 patients per day at each facility. 
RBOI has two locations in Marion County; one location near downtown Ocala and a second location in southwestern Ocala known as Timber Ridge. We also have a facility in Lecanto (Citrus County) and a facility in The Villages (Lake County). All facilities are within 30 miles of each other.
The ideal candidate would be ABR certified with a license to practice in the state of FL. Applicants in their final year of Medical Physics residency would be considered for the position. For applicants without a state license, Florida has a 2 year physicist in training license available. This is an onsite clinical position. The physicists routinely rotate through each of the 4 centers keeping a fresh set of eyes on clinical patients while being exposed to a wide variety of procedures. 
RBOI offers an attractive salary in agreement with the AAPM salary survey and a generous benefits package including 401k, medical/dental/vision insurance. All licensing/certification expenses and appropriate meeting/CE costs are included in the benefits package.
CONTACT: 
Tonya Painter, Operations/HR Director
<a href="mailto:tpainter@rboi.com" target="_blank">tpainter@rboi.com</a>
Bradley Beck, Chief Physicist
<a href="mailto:bbeck@rboi.com" target="_blank">bbeck@rboi.com</a>
2020 SE 17th Street
Ocala, Fl 34471
352-861-0440
Fax: 352-414-4866

Physicist

<h3>Job Description</h3>
Job Description
Geotechnical Engineer – Nationwide Opportunities
Earth Systems, LLC – part of EnviroTech Holdings (Earth Systems, EnviroTrac, EnviroTactics, Spangler Environmental, Bio-Tech Consulting, Earth Systems Response &amp; Restoration)
Looking for a career where your expertise actually makes an impact? At Earth Systems, we’re not your typical environmental consulting firm. With 30+ locations nationwide, our teams of scientists and engineers tackle geotechnical and environmental challenges head-on—combining technical know-how with practical solutions that matter.
Position Overview We’re looking for a Geotechnical Engineer who knows the consulting world—someone who’s worked with firms providing Geology, Environmental Science, and Environmental Engineering services. If you thrive in a fast-moving, multidisciplinary environment, this role will give you the chance to lead from the field and solve real-world problems head-on. You’ll take charge of project leadership across multiple regions, using your technical expertise and practical mindset to deliver results that matter.
The ideal candidate will hold a PE license and bring proven experience in the environmental consulting industry, with the confidence to step into a leadership role and the drive to make an impact.
What You’ll Do
<ul>
<li>
Lead geotechnical investigations and in-situ testing
</li>
<li>
Deliver foundation design, slope stability, and settlement analysis recommendations
</li>
<li>
Write and present clear, actionable reports for clients
</li>
<li>
Scope, budget, and manage projects with support from a collaborative team
</li>
<li>
Oversee fieldwork and lab testing to ensure QA/QC
</li>
<li>
Partner with clients, regulators, and project teams to keep work on track
</li>
<li>
Mentor junior staff and share your expertise
</li>
</ul>
What We’re Looking For
<ul>
<li>
Bachelor’s degree in Geotechnical Engineering, Geology, Environmental Engineering, or related field (Master’s a plus)
</li>
<li>
5+ years of experience in geotechnical or applied environmental consulting
</li>
<li>
PE license or EIT with the ability to obtain licensure in the state of hire within 12 months
</li>
<li>
Proficiency in AutoCAD, gINT, GeoStudio, or similar software
</li>
<li>
Strong writing skills and experience preparing technical reports
</li>
<li>
Willingness to travel to project sites within your region
</li>
</ul>
What We Offer
<ul>
<li>
Competitive salary and full benefits (medical, dental, vision, life)
</li>
<li>
401(k) with company match
</li>
<li>
PTO, holidays, and flexible scheduling
</li>
<li>
Phone reimbursement
</li>
<li>
Hybrid work (office/field/home mix)
</li>
<li>
Paid training, certifications, and continuing education
</li>
<li>
A growth-focused, collaborative culture where your voice matters
</li>
</ul>
At Earth Systems, you’ll have a seat at the table from day one—and the chance to shape meaningful projects that drive real change.
Ready to take the next step? Apply now!

621 Science Jobs