Cleveland Skin Pathology Laboratory is a private dermatopathology laboratory in Cleveland, Ohio. CSPL has been in operation for over 40 years, and provides diagnostic pathology services to dermatologists both within the state and nationally. CSPL processes approximately 65,000 specimens per year. A full time laboratory supervisor is currently being sought to manage our new facility in Beachwood, Ohio.

The laboratory supervisor will manage and coordinate all administrative and technical activities within the lab. This includes ensuring adequate supplies, properly maintained equipment and staff scheduling as to maximize efficiency and work flow. The laboratory supervisor will communicate lab policies with the staff, and conduct QA and QC studies and maintain documentation and standards as outlined by both CLIA and CAP. The laboratory supervisor will take responsibility for test validation and optimization of immunoperoxidase stains. The laboratory supervisor will have responsibility for organizing and communicating with laboratory personel to promote employee understanding and ensure that all duties are performed in a timely manner.

Bachelor’s degree with experience in laboratory procedures including grossing, embedding, microtomy, special stain techniques, and immunohistochemistry.

ASCP certification in either HT or HTL (preferred). The candidate should also have experience as a supervisor, possess a working understanding of compliance policies, management and decision making skills, ability to delegate responsibilities and cooperate with the laboratory staff.

Email Stephen Somach at scsomach@cleveskinpath.com or Fax 216-464-7531]]> 2009-11-04T14:10:05-05:00 en-us Copyright © 2009 craigslist, inc. http://cleveland.craigslist.org/sci/1451364199.html text 2009-11-04T14:10:05-05:00 http://cleveland.craigslist.org/sci/1450015136.html
• Must have experience in energetics, pyrotechnics, kinetics and or reactive materials.
• Will lead a specific program regarding energetics.
• Must have experience with reactive materials that will essentially replace phosphorous.
• Must be able to manage budgets, meet deadlines and handle tight schedules in an effective manner.
• Must have experience in writing SBIR proposals.
• There will be no training. Applicant must be self taught, very hands on and be able to take ownership of this program.
• Must be a US citizen.



Our Company is an advanced materials development firm focused on the production of bulk nanmaterial. We design, develop and manufacture metal and ceramic fine powders and particulates using fluidized bed Chemical Vapor Deposition technology. Our nanoencapsulation process displaces conventional milling and blending, melt atomization and spray drying processes for producing alloy and composite powders, while providing near-atomic level control over composition, purity and structure. This Company has the unique capability to engineer and manufacture alloy powders and particles down to submicron sizes, with aspect ratios up to several hundred. This is accomplished using proprietary, patented, R&D 100 Award winning (2000) core technologies to develop, engineer and manufacture highly differentiated metal, ceramic and composite materials. With these technologies, the company can both nanoegineer (engineer at the atomic level) materials and cost-effectively produce these materials in bulk. Our Company is using micro-and nanoengineered products enhance materials capabilities and/or reduce the cost of our client’s products and services. They also use value-added engineered raw materials are used in industrial manufacturing and services in many fields including: electronic materials (heat spreaders, capacitors and storage media): metal cutting and forming tools: abrasive friction and wear products (metal composite brake pads and pump seals) aerospace and defense (rocket engines, missiles and spacecraft propulsion and structures) paints, pigments and fillers for plastics and thermal spray coatings

HERE’S WHAT YOU WOULD BE DOING?
The Research Scientist organizes, executes and coordinates research investigations into advanced materials and processes including spray drying, thermal spray, milling, calcining, reduction, atomization, mocroenapsulation, extrusion, forging, hot pressing and reactive synthesis. The work involves research projects and pilot operations to evaluate conventional and pioneering developments in nanomaterials and advanced metals production and application, including armor, anti-armor, chrome replacement, thermal barrier coatings and others. Will be responsible for applying creative, professional and technical skills to solving materials synthesis, processing and applications problems.

Knowledge Skill: Requires graduate degree in materials related discipline and 3-10 years experience involving materials synthesis research. The ideal candidate will have a background in powder metallurgy, rolling, extrusion, process or product development or metallurgical or ceramic engineering.

Problem Solving/Decision Making: The research scientist receives specific project assignments and directions to attack and is responsible for execution of complex projects. Including developing information sources, points of emphasis, scope of work, possible solutions, and specific experimental approach. This position requires a high level of integrity and judgment/decision-making skills. The research scientist will be responsible for research projects from initiation to small scale pilot plant. The engineer shall develop alloys and compositions and develop grain size and microstructure control techniques for nano-crystalline metals and ceramic products and shall develop material and process specifications, complete process design and implement pilot scale production until the process is turned over to production. A large portion of this position will be managing grant proposals-seeking, writing, submitting and completion.

SO WHAT’S SO GREAT ABOUT THIS JOB ANYWAY?
Here are some of the fabulous benefits this Company Offers:
• 401K
• Education Assistance
• Paid Holidays
• Health Insurance
• Vacation Time


Please Submit Resumes to:
Email: hr@ppswork.com
Fax: 440-914-0109
]]> 2009-11-03T15:47:20-05:00 en-us Copyright © 2009 craigslist, inc. http://cleveland.craigslist.org/sci/1450015136.html text 2009-11-03T15:47:20-05:00 http://cleveland.craigslist.org/sci/1447508663.html 2009-11-01T23:27:56-05:00 en-us Copyright © 2009 craigslist, inc. http://cleveland.craigslist.org/sci/1447508663.html text 2009-11-01T23:27:56-05:00 http://cleveland.craigslist.org/sci/1443835734.html
Every day, Kelly Scientific Resources (KSR) Clinical Research connects scientific professionals with opportunities to advance their careers. We currently have an exciting 12 month temporary Clinical Research Assistant opportunity available in Cleveland, OH.

Please read the job description below, and then click on the 'APPLY NOW' button to take your career to new heights!

Responsible for study daily operations including:

'Conduct recruitment and enrollment of subjects.
'Participate in revision of study instruments and data collection protocols.
'Schedule study assessments for subjects.
'Carry out high-quality data collection.
'Perform data entry and cleaning, and assist with data management.
'Participate in the development of data code book.
'Conduct reliability checks for collected data and evaluate adequacy of research techniques.
'Prepare study materials, including instruments and questionnaires.
'Maintain study documents and materials; records keeping.
'Attend research meetings.
'Maintain good communication with PI, project manager, and research team members.
'Complete adequate job-related training.

Responsible for subject protection including:

'Assist with the IRB application, addendum, and continuing reviews.
'Responsible for subject protection in the consent process and during data collection; ensure adherence to the IRB protocol.
'Implement data safety plan, monitor and document adverse events.
'Complete annual renewal of IRB training in subject protection and IRB certification.
'Participate in dissemination of study findings including:
'Assist with preparation of abstracts, manuscripts, posters, and research presentations.
'Assist with annual progress report to be submitted to funding agency.
'Assist with preparation of grant proposals.
'Conduct literature review, including conducting and retrieving library searches.
'Present the study or study findings at local or regional meetings on behalf of the PI.

SUPERVISOR RESPONSIBILITY:

'Supervise graduate and undergraduate students who assist with data collection, entry, and analysis or observe to learn about research and data collection.

REQUIREMENTS:
Bachelor's Degree is required. Must have Three to five years previous research experience and two to three year clinical experience with patients in an in-patient or outpatient setting. Also required to have experience with the semi-structured interview with subjects.

'Ability to conduct qualitative study and semi-structured interview with patient subjects 'Ability to meet unexpected challenge and solve problems 'Proficient in computer software (Microsoft Office, SAS/SPSS) 'Know how to administer research instruments 'Know how to code semi-structured interview instrument 'Know how to assist with writing grant proposals

Kelly Scientific Resources (KSR) is the leading scientific and clinical research staffing company in the world. We employ more than 700 clinical research professionals and 4,500 scientists on an average workday on a temporary, project and full-time basis in a broad spectrum of industries and disciplines. KSR has more than 100 locations in North America, Europe and the Pacific Rim.

Please visit us at www.kellyscientific.com to learn more.

Kelly Services is an Equal Opportunity
Employer.

RESPOND HERE! To respond immediately, access the online response form at: http://sh.webhire.com/servlet/resp/rf?jobid=2404334&boardid=1905]]> 2009-10-30T00:35:43-04:00 en-us Copyright © 2009 craigslist, inc. http://cleveland.craigslist.org/sci/1443835734.html text 2009-10-30T00:35:43-04:00 http://cleveland.craigslist.org/sci/1443768315.html The territory is based in the Midwest Region and will cover Ohio and Kentucky. Abbott Laboratories is seeking a Regional Clinical Research Associate (RS-CRA) for a their US Clinical Field Operations Team. The RS-CRA will be directly responsible for conducting site qualification, initiation, interim monitoring and study closeout visits in accordance with all applicable regulations, guidelines, and business processes and will monitor the activities of clinical investigative sites across multiple protocols and multiple therapeutic areas. Report monitoring activities and study site conduct via written reports. Interact and build professional and collaborative relationships with all study personnel, peers and office-based personnel. Use multiple technologies to maintain open and frequent communication with Abbott and site personnel. The RS-CRA will partner with other Abbott personnel to develop innovative processes and technologies to increase the quality, productivity, and efficiency of Abbott US Clinical Field Operations and create a positive work environment by encouraging mutual respect, innovation and accountability at all levels. The RS-CRA will be responsible for assignments of greater complexity (i.e., greater number of sites, site participating in more complex clinical studies, sites requiring more oversight of operational issues). The RS-CRA ensures regulatory inspection readiness at assigned clinical sites. Additionally, the RS-CRA may train and provide guidance to junior staff. Position functions in an independent and regionally based capacity.

QUALIFICATIONS:

Skills/Experience Requirements:

- Demonstrate strong site management and monitoring skills
- Exhibits strong planning and organizational skills and the ability to work effectively and
efficiently in a dynamic environment with competing projects and deadlines
- Excellent written and verbal communication skills
- Acute observational skills, analytical and conceptual capabilities
- Exhibit high degree of flexibility when facing changes in the work environment
- Proficiency in the use of personal computers, including experience with EDC, CTMS, word
processing, spread sheets, email, and web-browser applications
- Strong ability to work independently with minimal supervision
- Excellent knowledge of regulations governing clinical research, ICH/GCP Guidelines
and/or federal regulations, and applicable local regulations
- Ability to proactively identify issues that may impact enrollment and recruitment timelines.
Collaborate with senior staff to develop initiatives and contingencies to ensure that
timelines are met
- Participate in and or present at departmental or investigator meetings. Participate in special
projects/work groups
- Build relationships with current investigators and identify, evaluate and recommend
new/potential investigators/sites on an on-going basis

Qualifications:
Minimum of 5 years of clinically related experience, of which 3 years must be in clinical research monitoring. Candidates with lesser experience will be considered.

Preferred Qualifications

- Experience in multi-therapeutic areas preferred - MS, MA, MBA, MPH desired

Through numerous local, national and international accolades, Abbott is regarded as an employer of choice for our commitment to workplace excellence. Our employees are given the tools to succeed, lead and grow, with challenging opportunities and work that makes a difference. Through our diverse healthcare businesses, we connect people and potential in ways that no other company can.

If interested, please apply online at http://track.jobviper.com/ViewJob.asp?id=649341-1248-1236