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<h3>Job Description</h3>
Job Description
Are you a passionate Research Scientist with a background in hematology and regenerative medicine? Do you want to take your career to the next level in a fast-paced and innovative environment?
Biofyl Scientific Research, a leader in regenerative medicine for over 20 years, is seeking a talented and driven scientist to join our team. We specialize in hematology and autologous biologics research, providing expert scientific services for regulatory, marketing, and R&amp;D purposes. If you are a technical expert who thrives on high-level lab work and enjoys method development, we want to hear from you.
This is a unique opportunity that requires relocation to the Fort Myers, Florida area. Qualified applicants will receive a signing bonus after a probationary period.
What You'll Do: Key Responsibilities:
As a key member of our laboratory team, you will play a crucial role in the execution of our research projects and daily operations. Your expertise will be essential in:
<ul>
<li>Handling and Analyzing Samples: You will work extensively with blood and bone marrow samples, performing advanced lab techniques such as Optical aggregometry, ELISA, Flow cytometry, Cell culture, and Microscopy.</li>
<li>Conducting and Managing Research: Efficiently perform investigational studies following established SOPs while ensuring the accuracy of all test results before reporting.</li>
<li>Maintaining Lab Excellence: Contribute to the day-to-day operations of the lab, including instrument maintenance, quality control, method setup, and troubleshooting.</li>
<li>Data Management: Meticulously maintain and manage data records, including regular data entry and archiving, while upholding strict confidentiality.</li>
</ul>
What We're Looking For:
Non-Negotiable Qualifications:
<ul>
<li>A Bachelor of Science degree in Biotechnology, Cell Biology, Molecular Biology, or a closely related field.</li>
<li>A minimum of two years of hands-on experience in a lab scientist or similar role.</li>
<li>Advanced working knowledge of laboratory equipment, processes, and Microsoft Office products.</li>
</ul>
Preferred Qualifications:
<ul>
<li>A Master's or Ph.D. in a relevant field.</li>
<li>Demonstrated ability to perform complex sample preparation and procedures.</li>
</ul>
Ready to make a move and join a leading team in regenerative medicine? Apply today and launch your career in sunny Fort Myers!
Company DescriptionBiofyl Scientific Research (formerly BioSciences Research Associates) is an independent contract research laboratory providing scientific services to Pharmaceutical and Biotechnology companies for product development and clinical trial support. We are located in Fort Myers, Florida. 
<h3>Company Description</h3>
Biofyl Scientific Research (formerly BioSciences Research Associates) is an independent contract research laboratory providing scientific services to Pharmaceutical and Biotechnology companies for product development and clinical trial support. We are located in Fort Myers, Florida.

Regenerative Research Scientist - Biofyl Laboratory

<h3>Job Description</h3>
We are currently looking for a skilled Analytical Chemist to join our dynamic team. As a company dedicated to excellence in Animal Health, we value individuals who are passionate about the quality of our products!
 
Primary Function: 
The Quality Control Chemist is a support role for the functioning of the Quality Control Laboratory and the Quality needs of the Compounding department. Support shall be provided by assisting the QC department in general to meet the departmental expectations for physical testing of products and materials which typically includes organoleptic evaluations, pH, Viscosity &amp; specific gravity. Supporting compounding department with tank cleaning verification testing and inspections as well as in-process manual batch adjustments and occasional laboratory trial sample preparations. Basic decision-making skills are required for this position. Examples for decision making skills include prioritize work, managing your time. Working toward continuous improvement efforts.
 
Key Responsibilities: 
· Evaluate in- process, Finished goods, R&amp;D and Stability samples for physicals analysis.
· Provide in-process batch adjustments by performing analysis and lab trails as instructed per the master batch record.
· Record all evaluations in the laboratory notebook and report test results in the appropriate forms and analysis sheets according to cGMP, SOP, and current industry practices.
· Clean and maintain a clean work area which includes cleaning glassware, counters, and equipment.
· Keeping the analytical laboratory supplies stocked and in order.
· Perform daily calibrations / verification of balances, viscometers, pH meters, conductivity meters and other such equipment or instruments used to perform the analysis.
· Monitoring supply inventory and notifying the management when it is time to order more supplies.
· Server as back-up to perform occasional R&amp;D work by preparing laboratory batches and or trials as instructed by the R&amp;D manager.
· Support Microbiology with basic solution/media preparation or basic testing on a back-up basis.
· Train new associates in QC laboratory on how to perform in-process batch adjustments and other functions as instructed by management.
· Other duties as assigned by management.
Skills &amp; Knowledge Required:
· Preferred degree in Chemistry or Related Scientific field
· Experience with HPLC analysis Waters brand preferred, Empower 3 Software
· Experience and skill with analytical weighing, pipetting, general analytical lab skills including related calculations.
· Experience with GMP / FDA regulated industry preferred
· Proficient with Microsoft Office Suite, including Outlook, Word, Excel
· Read, Write, Comprehend SOP, Compendia, Technical documents in English

Analytical Chemist

<h3>Job Description</h3>
Job DescriptionChemist II
Job Description
We are seeking a meticulous and skilled Chemist II to join our team. The candidate will perform a range of laboratory testing and support functions to ensure the quality and integrity of our products. The role requires expertise in both wet chemistry and instrumental analysis, contributing to our continuous improvement initiatives.
Responsibilities
<ul>
<li>Conduct testing including TLC, FT-IR, and composition testing with proficiency in following USP monographs and general chapters.</li>
<li>Perform wet chemistry testing such as loss on drying, pH, titrations, and solution preparations.</li>
<li>Support daily laboratory operations including glassware cleaning, solvent waste disposal, and daily/weekly balance calibrations.</li>
<li>Assist upper-level Quality Control Chemists as needed.</li>
<li>Perform strength testing using HPLC, GC, and/or ICP.</li>
<li>Contribute to process and continuous improvement efforts.</li>
<li>Complete all other duties as assigned by the Quality Control Lab Supervisor/Management.</li>
<li>Willingly work holidays and weekends as requested.</li>
</ul>
Essential Skills
<ul>
<li>Proficiency in chemistry, HPLC, and gas chromatography.</li>
<li>Experience in wet chemistry and quality control under GMP conditions.</li>
<li>Ability to operate, analyze data, and troubleshoot general lab instrumentation.</li>
<li>Capability to interpret data based on internal specifications and USP requirements.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Strong attention to detail and organizational skills.</li>
<li>Ability to multitask and manage samples efficiently.</li>
<li>Adaptability to learn and adhere to cGMP, 21 CFR 111, SOPs, and Batch Records.</li>
<li>Knowledge of 21 CFR 210 and 211 is desirable.</li>
<li>Proficiency in computer software such as Word, Outlook, PowerPoint, and Excel.</li>
<li>Excellent interpersonal and communication skills in English.</li>
</ul>
Work Environment
The work environment is a laboratory setting that involves handling chemicals and operating various lab instruments. The role may require working on holidays and weekends as needed. The candidate should be comfortable with the dress code appropriate for a laboratory environment.
Pay and Benefits
The pay range for this position is $26.44 - $31.25/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Largo,FL.
Application Deadline
This position is anticipated to close on Oct 6, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Chemist II

<h3>Job Description</h3>
Clinical Laboratory Supervisor needed!
 
Shift time: M-F Daytime
 
Position Summary:
The Laboratory Supervisor is accountable for the accuracy and reliability of all laboratory services provided by the specialty department section under his/her immediate control. The Laboratory Supervisor is responsible for day to day supervision and oversight of the laboratory operation, personnel and for monitoring processes to ensure that acceptable levels of performance are maintained.
 
The Laboratory Supervisor is also responsible for helping in the implementation of all area procedures and operations as well as ensuring that metrics established to measure quality, production and efficiency are strictly followed.
 
Responsibilities:
<ul>
<li>Under the direction of, and in the absence of the Laboratory Manager and/or Medical Laboratory Director, the Laboratory supervisor ensures adequate performance of all laboratory procedures</li>
<li>Performs high complexity clinical tests by following department procedures as needed (frequency not to exceed applicable state regulations for exempt employees).</li>
<li>Presents data and/or information across all levels including the lab, department, division, and corporate, and proficiently answers questions from all groups of staff, managers, and clients</li>
<li>Develops and maintains detailed laboratory procedures manual to meet accreditation and licensing requirements; ensures departmental SOP’s accurately reflects the current process; updates SOP’s as needed</li>
<li>Provides direct supervision of the laboratory operation and personnel performing high complexity testing and reporting of test results by qualified technologists</li>
<li>Initiates and monitors QC programs for the department; assures compliance with regulations; monitors all quality metrics and ensures that corrective actions are documented and implemented</li>
<li>Responsible for the selection, retention, and training of qualified laboratory personnel; ensures that Laboratory staff is trained and compliant with SOP’s and Skills checklists</li>
<li>Prepares employees reviews, approves time and attendance records, maintains training files and performs other administrative duties as required</li>
<li>May assist the Laboratory Manager or Director of Operations in establishing budgetary controls and maintaining cost at an acceptable level. May prepare reports detailing departmental activities, revenues, expenses and the like, as needed</li>
<li>Perform other duties as assigned by the Laboratory Manager or Laboratory Director</li>
</ul>
 
Experience, Education and Qualifications:
Master of Arts or Master of Science Degree from an accredited institution with a major in one the chemical, physical, or biological sciences, and subsequent to graduation, has had at least four years of pertinent laboratory experience of which not less than two years have been spent working in a clinical laboratory having a director at the doctoral level
-OR-
 
Bachelor’s Degree from an accredited college or university in one of the chemical, physical, or biological sciences with the addition of the successful completion of a course of at least 1 year. At least 6 years of pertinent clinical laboratory experience subsequent to qualifying with 2 of those years spent working in a clinical laboratory with a director at the doctoral level
 
At least six (6) or more years' experience (high complexity testing) preferred in the assigned specialty. (A minimum of one (1) year of internal service in the designated specialty as a Clinical Laboratory Technologist III is typically required for promotion to this level.)
At least three (3) or more years of successful experience in a supervisor or leadership capacity preferred
 
Certificate Compliance Requirements:
<ul>
<li>Nationally: ASCP certification for the assigned specialty, as available</li>
<li>FL: current state supervisor level license to perform laboratory testing</li>
<li>CA: current state supervisor level license to perform laboratory testing</li>
<li>TN: current state supervisor level license to perform laboratory testing</li>
</ul>

Clinical Laboratory Supervisor

<h3>Job Description</h3>
Job Description
We are a fast-growing medical device company developing advanced Software as a Medical Device (SaMD) solutions for interventional cardiology and structural heart procedures. Our flagship technology integrates real-time fluoroscopy with pre-procedure 3D CT annotations to provide precise intra-procedural guidance, enhancing safety and clinical outcomes.
Our innovation combines CT preprocessing, fluoroscopy preprocessing, AI-driven detection and tracking, anatomical landmark detection, and personalized DRR-based network training with cutting-edge registration protocols. We operate with a small, highly skilled in-house engineering team, supplemented by specialized contractors across several continents.
Summary: We are seeking a dynamic Director of Technology, Research &amp; Development to lead a team of engineers in our start-up medical device company. This role involves overseeing the R&amp;D pipeline, ensuring alignment with regulatory and market demands, and spearheading the development of groundbreaking technologies that enhance our company's growth and competitive advantage. The position is fully remote and reports directly to the Founder.
Stand out candidates should have experience in one or more of the following:
<ol>
<li>Heart CT imaging</li>
<li>Heart real time fluoroscopy.</li>
<li>Registration of the two modalities</li>
<li>Working with AI for segmentation and detection</li>
<li>Understanding 3D to 2D geometrical consideration</li>
</ol>
Responsibilities
1. Strategic Leadership:
<ul>
<li>
<ul>
<li>Lead and manage a remote team of freelancers and employees in the R&amp;D department.</li>
<li>Oversee the research and development pipeline, ensuring alignment with business goals and market needs.</li>
<li>Drive innovation in medical device technologies to maintain competitive advantage.</li>
<li>Collaborate closely with executive leadership, including product development, regulatory, and commercial teams, to ensure alignment across departments.</li>
<li>Ensure compliance with regulatory standards and guidelines.</li>
<li>Report regularly to the Founder on R&amp;D progress, challenges, and opportunities.</li>
</ul>
</li>
</ul>
2. Research and Development Oversight:
<ul>
<li>Oversee all stages of product research and early development, from ideation through feasibility and prototyping.</li>
<li>Manage the development of the user interface for procedural workflow integration.</li>
<li>Drive efficient design, testing, and validation of new devices in compliance with industry standards and regulations (e.g., FDA, ISO 13485)</li>
<li>Oversee data storage and management systems, ensuring compliance with healthcare data security regulations (e.g., HIPAA, GDPR).</li>
<li>Coordinate data engineering tasks, including structured pipelines for AI training datasets.</li>
</ul>
3. Technology Innovation and Advancement:
<ul>
<li>Develop and optimizeAI-based detection and tracking algorithms, ensuring robustness in procedural conditions.</li>
<li>Promote a culture of innovation and scientific excellence within the organization.</li>
<li>Partner with external stakeholders (clinical sites) for collaborative innovation and research.</li>
</ul>
4. Regulatory and Quality Collaboration:
<ul>
<li>Ensure all research activities align with medical device regulations and quality system requirements.</li>
<li>Support regulatory strategy development by providing technical and scientific input.</li>
</ul>
5. Talent and Organizational Development:
<ul>
<li>Recruit, develop, and retain top engineers and technical talent.</li>
<li>Foster team collaboration, mentoring, and continuous professional development.</li>
</ul>
Ideal Candidate Profile:
<ul>
<li>Advanced degree (Ph.D. or Master's) in engineering, biomedical sciences, or a related field.</li>
<li>10+ years of leadership experience in R&amp;D within the medical device or life sciences industry.</li>
<li>Demonstrated success in bringing medical devices from concept through commercialization.</li>
<li>Background in software development, image registration and AI</li>
<li>Strong understanding of FDA regulations, ISO standards, and global medical device requirements.</li>
<li>Visionary leader with excellent communication, strategic thinking, and stakeholder management skills.</li>
<li>Ability to work and manage in a remote environment.</li>
</ul>
We are currently expanding our team. As a start-up, we are fast paced and have a shared goal to succeed in developing unmet healthcare needs in the most efficient way. If you share this vision and are interested in joining us - please apply. We look forward to hearing from you.

Director of Technology, Research and Development

<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 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

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