Employment Screening Processes Sample Clauses

Employment Screening Processes. Once candidates are identified, they undergo a rigorous multi-part screening to evaluate technical capability and competence; communication and interpersonal skills; professional knowledge; and career progress. The recruiting team verifies employment history, clearance status, and academic degrees. During the qualification process, several tools/resources are utilized to ensure the best talent is identified, and the right hiring decisions are made. Tools/resources utilized include: • Skills Validation: HackerRank for Work is an innovative approach to assess candidate technical skills and experience. Datawiz uses this tool to create programming challenges of varying difficulty based on job specific requirements.
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Employment Screening Processes. We provide the following employment screening processes that are utilized by Tal Search Group to recruit consultant candidates under the IT State Term Contract as well as other recruitment contracts.
Employment Screening Processes. Atlantix Partners uses a combination of in-house and third-party resources to screen and verify prospective and current employees. Our employment hiring process involves several layers of screening and addresses an individual’s technical acumen and experience, personal traits, and background. As candidates are identified, we perform an initial technical screen interview. Candidates of interest then proceed through a series of interviews with Human Resources, Project Team members, and firm leadership. Before hiring an individual, we conduct background checks and verify references. Our third- party resource First Choice conducts our background checks which include a review of an individual’s education, employment, credit, and criminal history, motor vehicle license record, and a drug screen. In addition to traditional background checks and personal interviews, Atlantix Partners uses The Predictive Index tests to understand and predict behavior, measure cognitive ability, and evaluate job matches.
Employment Screening Processes. All applicants are required to submit a resume, application questionnaire (listing education and work history), as well as copy of any certifications/licenses earned. Once a contingent offer of employment is extended, a third-party conducts a thorough background check, including Social Security trace; Sex Offender Database check; national, state and county background check (the past 7 years, up to 2 additional AKAs); education verification; E-Verify; and drug screen. JET directly conducts the Employment Verification for the last 3 employers or up to the past 10 years. Candidates are also screened according to the specific customer requirements for the company and the position, as it relates to education, certifications, skill set and background screening requirements. JET’s employment practices adhere to all state, Federal and local laws, including FLSA, FMLA, OSHA, EEOC and other regulations.
Employment Screening Processes. Verifying qualifications and skills of the prospective employees is paramount. We apply rigorous quality controls in all aspects of recruitment, vetting, and registrations to ensure that all our candidates exceed the regulatory standards set by the Client. ✓ For DC, we screened over 33,000 resumes delivered over candidates. and 600 ✓ For PA, we screened 17,000 resumes and provided over 1,000 candidates We utilize our reach, automation, and best practices during sourcing— integrated by our ATS—so that we can focus on vetting each identified candidate. Once we identify qualified candidates via one of the sources described above, OST deploys a rigorous cross- organizational interview and screening process. We perform this screening and interview process for all candidates, regardless of whether they come from a subcontractor or us. Our screening process is an in-depth assessment of each candidate’s fit and function for a given role. position. Also, depending on the SLA and DMS’s requirements, we will proactively begin reference and background checks to expedite the onboarding process in anticipation of candidate selection. OST applies stringent standards during the hiring process and as well as after the onboarding of the candidate. Before hiring, OST ensures that our candidates have passed the necessary background checks and require any subcontractor working on the project to follow the same performance and background check standards. This is a part of our sub-contractor agreement and ascertains that DMS only receives qualified and vetted candidates for consideration. We have the following standards after onboarding: Our most recent average customer satisfaction rating of 9.5 out of 10 for DC and PA demonstrate the quality of our services. With 19+ years of IT staffing experience, we have learned how important it is to monitor the performance of our placed employees continuously. Throughout each engagement, our CM will work closely with the DMS management to ensure our resources continue to perform at the highest level to complete deliverables. Also, we apply ISO 10002:2015 (Quality Management – Customer Satisfaction) processes to enhance our customers’ experience through regular feedback sessions and surveys. Furthermore, our CM will continuously monitor resources’ performance by using the following methods: . ✓ ✓ Performance Monitoring: After onboarding, OST will draw the performance management plan which will list employee’s performance elements. These pe...
Employment Screening Processes. Business Integra implements a comprehensive pre-screening process to correctly evaluate candidates and make sound hiring decisions. Our recruiters will employ our proven pre-screening methodologies to deliver quality results for the State of Florida. We have a dedicated technical team to perform the following screening processes.
Employment Screening Processes. Employment Standards Validation of Education Fit of Resume to State’s Job Title Description
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Employment Screening Processes 

Related to Employment Screening Processes

  • Training Programs All employees shall successfully complete all necessary training prior to being assigned work (e.g., all employees will complete health and safety training prior to being assigned to task). Nothing in this Article or provision shall constitute a waiver of either party’s bargaining obligations or defenses. The Employer still has an obligation to notify and bargain changes in terms and conditions of employment with the exclusive representative.

  • Training Program It is agreed that there shall be an Apprenticeship Training Program, the provisions of which are set forth in Exhibit "D", which is attached hereto and forms part of this Agreement.

  • Research Program The term “Research Program” shall mean the research program to be undertaken by TSRI under the direction and control of the Principal Investigator as expressly set forth on Exhibit A hereto.

  • TRAINING AND EMPLOYEE DEVELOPMENT 9.1 The Employer and the Union recognize the value and benefit of education and training designed to enhance an employee’s ability to perform their job duties. Training and employee development opportunities will be provided to employees in accordance with Employer policies and available resources. 9.2 Attendance at employer-required training will be considered time worked. The Employer will make reasonable attempts to schedule employer-required training during an employee’s regular work shift. The Employer will pay the registration and associated travel costs in accordance with Article 23, Travel, for employer-required training.

  • Research Use Reporting To assure adherence to NIH GDS Policy, the PI agrees to provide annual Progress Updates as part of the annual Project Renewal or Project Close-out processes, prior to the expiration of the one (1) year data access period. The PI who is seeking Renewal or Close-out of a project agree to complete the appropriate online forms and provide specific information such as how the data have been used, including publications or presentations that resulted from the use of the requested dataset(s), a summary of any plans for future research use (if the PI is seeking renewal), any violations of the terms of access described within this Agreement and the implemented remediation, and information on any downstream intellectual property generated from the data. The PI also may include general comments regarding suggestions for improving the data access process in general. Information provided in the progress updates helps NIH evaluate program activities and may be considered by the NIH GDS governance committees as part of NIH’s effort to provide ongoing stewardship of data sharing activities subject to the NIH GDS Policy.

  • Screening After you sign and date the consent document, you will begin screening. The purpose of the screening is to find out if you meet all of the requirements to take part in the study. Procedures that will be completed during the study (including screening) are described below. If you do not meet the requirements, you will not be able to take part in the study. The study investigator or study staff will explain why. As part of screening, you must complete all of the items listed below: • Give your race, age, gender, and ethnicity • Give your medical history o You must review and confirm the information in your medical history questionnaire • Give your drug, alcohol, and tobacco use history • Give your past and current medication and treatment history. This includes any over-the-counter or prescription drugs, such as vitamins, dietary supplements, or herbal supplements, taken in the past 28 days • Height and weight will be measured • Physical exam will be done • Electrocardiogram (ECG) will be collected. An ECG measures the electrical activity of the heart • You may be tested for COVID-19 o Blood tests for human immunodeficiency virus (HIV), hepatitis B, and hepatitis C o Blood tests to see how your blood clots ▪ Fibrinogen ▪ PT/INR/aPTT o Blood tests for amylase and lipase (enzymes that help with digestion, Part B only) o Blood tests for a lipid (fats) panel (Part B only) ▪ Total cholesterol ▪ Triglycerides ▪ HDL ▪ Direct HDL o Blood tests to check your thyroid function (Part B and Part C only) ▪ TSH ▪ Free T4 o Urine to test for drugs of abuse (illegal and prescription) o Urine tests to check your albumin/ creatinine ratio o Females who have not had a period for at least 12 months in a row will have a blood hormone test to confirm they cannot have children • The study investigator may decide to do an alcohol breath test • The use of proper birth control will be reviewed (males only) • You will be asked “How do you feel?” HIV, hepatitis B, and hepatitis C will be tested at screening. If anyone is exposed to your blood during the study, you will have these tests done again. If you have a positive test, you cannot be in or remain in the study. HIV is the virus that causes acquired immunodeficiency syndrome (AIDS). If your HIV test is positive, you will be told about the results. It may take weeks or months after being infected with HIV for the test to be positive. The HIV test is not always right. Having certain infections or positive test results may have to be reported to the State Department of Health. This includes results for HIV, hepatitis, and other infections. If you have any questions about what information is required to be reported, please ask the study investigator or study staff. Although this testing is meant to be private, complete privacy cannot be guaranteed. For example, it is possible for a court of law to get health or study records without your permission.

  • Progressive Discipline Both parties endorse the principle of progressive discipline as applied to professionals.

  • Collaboration 31.1 If the Buyer has specified in the Order Form that it requires the Supplier to enter into a Collaboration Agreement, the Supplier must give the Buyer an executed Collaboration Agreement before the Start date. 31.2 In addition to any obligations under the Collaboration Agreement, the Supplier must: 31.2.1 work proactively and in good faith with each of the Buyer’s contractors 31.2.2 co-operate and share information with the Buyer’s contractors to enable the efficient operation of the Buyer’s ICT services and G-Cloud Services

  • Research Plan The Parties recognize that the Research Plan describes the collaborative research and development activities they will undertake and that interim research goals set forth in the Research Plan are good faith guidelines. Should events occur that require modification of these goals, then by mutual agreement the Parties can modify them through an amendment, according to Paragraph 13.6.

  • Development Program RWJPRI shall be [**] and have [**] in consultation with the JDAC, to select LICENSED COMPOUNDS which shall then be designated PRODUCTS for further DEVELOPMENT by RWJPRI and marketing by ORTHO and its AFFILIATES. RWJPRI shall provide KOSAN with written notice of its decision to select a LICENSED COMPOUND for DEVELOPMENT. Once a PRODUCT has been selected for further DEVELOPMENT, RWJPRI, with the advice of the JDAC, shall have the [**] right to develop the PRODUCT through STAGES O, I, II and III and shall have the [**] right to prepare and file, and shall be the owner of, all applications for MARKETING AUTHORIZATION throughout the world. During such DEVELOPMENT efforts, KOSAN will assist RWJPRI as may be mutually agreed, at RWJPRI's expense, in chemical development, formulation development, production of labeled material and production of sufficient quantities of material for STAGE O and initial STAGE I studies. RWJPRI shall exercise diligent efforts, commensurate with the efforts it would normally exercise for products with similar potential sales volume and consistent with its overall business strategy, in developing such PRODUCT in accordance with the DEVELOPMENT PLAN established by RWJPRI. In the course of such efforts RWJPRI shall, either directly or through an AFFILIATE or SUBLICENSEE to which the license shall have been extended, take appropriate steps including the following: (i) in consultation with the JDAC, select certain LICENSED COMPOUNDS for STAGE O DEVELOPMENT; and (ii) establish and maintain a program reasonably designed, funded and resourced to obtain information adequate to enable the preparation and filing with an appropriate and properly empowered national regulatory authority all necessary documentation, data and [**] CERTAIN INFORMATION IN THIS EXHIBIT HAS BEEN OMITTED AND FILED SEPARATELY WITH THE COMMISSION. CONFIDENTIAL TREATMENT HAS BEEN REQUESTED WITH RESPECT TO THE OMITTED PORTIONS. other evidence required for IND non-rejection to commence and conduct human clinical trials of such PRODUCT. (iii) proceed following IND non-rejection to commence PHASE I, II, and III clinical trials, associated studies and such other work which RWJPRI reasonably deems to be required for subsequent inclusion in filings for MARKETING AUTHORIZATION; (iv) after such submissions are filed prosecute such submissions and file all reasonably necessary, reports and respond to all reasonable requests from the pertinent regulatory, authorities for information, data, samples, tests and the like.

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