Total 159 science rd research job vacancies in panama city torre v

Do you have experience in working with library collections? Can you provide a friendly and welcome presence to our users, guiding them to the right information sources?

About us

This is an exciting time for SMG's Archives and Libraries with our new strategy setting out how our collections will be the best in the world in our fields: well-understood, well-housed and accessible (physically and digitally) and used effectively by us and others for research, display, learning and pleasure.

The Dana Research Centre and Library at the Science Museum, provides open access to around 7,000 books and periodicals covering the history and biography of science, technology, and medicine, as well as providing access to the Science Museum's rich collections of archives and rare books.

To support the library, we are now seeking a Senior Archive and Library Assistant to be based at the Science Museum in London, on a full time permanent basis.

About the role

This new role will work closely with the Science Museum Librarian, Systems and E-resources Librarian, Collections and Research and Public History teams to support the Science Museum's priorities, and the development and intellectual care of the collection. You will play a key role in providing access to Dana Research Centre and Library. You will be responsible for ordering and cataloguing library material, including for other sites, maintaining the public library space, and supporting access to archives and rare books.

Download the Vacancy Information Pack file under 'Attachments' on this vacancy listing on the Science Museum Group website for more details about the role and the application process.

About you

You will bring excellent customer service skills with experience in working with library collections, particularly cataloguing. You will be comfortable speaking to a range of people, demonstrating active listening skills and able to prioritise effective and remain courteous under pressure. You will have good ICT and organisational skills, as well as good attention to detail.

Don't feel you meet all the criteria? We welcome you to apply even if your experience doesn't match directly. With your transferable skills, you could be the right candidate for this, or other opportunities that we have.

What we offer

Joining us as an employee, you will have the opportunity to develop your career in a world-class museum group. We understand that work/life balance and wellbeing is crucial to our colleagues, so we offer the perks listed below, as well as support for things that happen in life such as parental and adoption leave, sickness, and career breaks.

• Support with personal and professional development
• 27 days annual leave in addition to bank holidays
• Employee assistance programme
• Enhanced contributory pension
• Unmind App and other wellbeing support
• Interest-free loans
• Days Out discounts
• Health & Dental Insurance

Open for All is one of the Science Museum Group's five core values and sets out our important aspiration to be a place for everyone. We are working hard to understand our organisation better and to develop a culture that recognises and values different backgrounds, mindsets, skills, experience, knowledge, and expertise. By having greater diversity, we believe that we will be a stronger and better organisation, capable to continue to Inspire Futures.

This position is located in New York, NY, within the ILR School located at 570 Lexington Avenue.

The School of Industrial and Labor Relations at Cornell University has an immediate opening for a Research Support Specialist – Research Support Specialist C06 in the Climate Jobs Institute in the Extension/Outreach Division with a focus on the intersection of labor, employment, and climate change.

Our Team:

The Climate Jobs Institute at Cornell University’s ILR School is guiding New York and the nation’s transition to a strong, equitable, and resilient clean energy economy that tackles the climate crisis, creates high-quality union jobs, and builds a diverse and inclusive workforce centering frontline communities.

Through cutting-edge policy research, deep relationships with on-the-ground partners, and innovative training and education programs, the Institute provides the information that policymakers, the labor and environmental movements, industry leaders and others need to navigate this historic transition to a zero-carbon economy.

The Climate Jobs Institute serves as the academic and educational partner to the Climate Jobs National Resource Center, providing research, policy, and educational support to coalitions of unions in numerous U.S. states.

What we are seeking:

The Research Support Specialist will support the research functions of the Climate Jobs Institute (CJI) program and contribute to and author independent research projects and collaborate with CJI faculty, staff, and ILR students on ongoing applied and academic research projects. Research work may involve conducting fieldwork related to research projects and collecting and analyzing information from archives, libraries, and other data and information centers. The individual will write and edit research reports, analyze current research and public policy, compile information and statistics, and generate literature reviews of ongoing research and education projects.

The position will provide legal research and analysis to support policy development and recommendations at the local, state, and national levels. This will involve using tools such as Lexis, Westlaw, and PowerSuite to understand complex regulatory environments in the fields of labor, energy, administrative, constitutional, contract, and employment law, and translate that research into presentations, policy reports, and internal memoranda.

The Research Support Specialist will also provide research assistance and perform research work for educational programs, including preparing presentations and crafting materials for CJI trainings. The individual will present at, participate in, and attend conferences, workshops, and public events related to research topics. The Research Support Specialist will work with undergraduate student fellows at the CJI. The individual will also edit grant and funding proposals, and write media articles for the CJI and ILR communications related to research topics.

This is a term, full-time, bargaining unit position that falls under the NYC ILR Extension exempt CWA contract. Initial appointment through June 30, 2025, position may be reappointed with approval based on available funding and work.

The position is based in the Cornell University, New York City ILR Extension office located at 570 Lexington Ave, New York, NY 10022.

More information about the ILR School can be obtained at our web site, http://www.ilr.cornell.edu and Climate Jobs Institute at https://www.ilr.cornell.edu/climate-jobs-institute

What we need:

• Bachelor’s degree and two to three years of relevant experience, education, or equivalent combination.

• Experience conducting legal research and analysis in a law firm, legal department, or similar environment.

• Demonstrated ability to write research reports/manuscripts for publication using appropriate style guides.

• Extensive experience with editing documents and research reports for publication.

• Ability to prepare presentations, create slides, and craft documents for educational programs and trainings.

• Experience in translating research/evaluation and complex concepts for a general audience.

• Ability to work on multidisciplinary teams, providing creative and critical independent thinking while also considering diverse opinions and approaches.

• Experience or internship working with unions, labor boards, or academic labor programs.

• Experience with internet, Lexis/Westlaw, and library searches.

• Good familiarity with many of the following areas including labor unions, especially building trade and energy sector unions, worker organizing and collective bargaining contracts, climate protection and clean energy policy, renewable energy and other low-carbon economic sectors, low-wage precarious work and inequality, and union and worker training programs.

• Must be able to manage multiple competing deadlines and be flexible with changing work priorities.

• Capable of working independently for long stretches of time with limited supervision.

• Capable of working in a collaborative environment.

• Excellent verbal, written, telephone and public presentation skills.

• Advanced experience with preparing, creating, and transforming academic citations in multiple formats such as APA, MLA, and Bluebook.

• Experience and skill using and learning different software packages and web-based tools (e.g., Microsoft Office, Zoom or videoconferencing software, Lexis Nexis, library databases, and Qualtrics).

• Experience in and/or demonstrated commitment to supporting diversity, equity, access, inclusion, and wellbeing.

• Passionate about working in an organization that values and promotes diversity, equity, inclusion, anti-racism, and wellbeing.

You will be a top candidate with our preferred qualifications:

• Master’s or advanced degree in public policy, law, labor relations, or related discipline.

• Prior experience working in climate change, labor, or policy communication.

• Four to five years of experience in research and/or program evaluation environment.

• Experience working in a team environment, providing collaborative input, and contributing support to creative database projects. 

• Ability to manage large datasets and extrapolate from data for use in public policy analysis.

• Knowledge of the construction industry, public sector procurements, or union organizing.

• Extensive knowledge of the offshore wind industry including the manufacturing supply chain, emerging clean energy technologies, New York state public policy on climate and offshore wind, and labor standards for renewable and clean energy projects.

• Research experience with reviewing and examining collective bargaining agreements.

• Capability to perform public policy research and understand the decision-making and law-making process of multiple states, federal, and international contexts.

• Knowledge of Canva and InDesign is preferred.

• Working knowledge of Spanish (or other foreign languages).

Salary meets New York City minimum exempt threshold of $62,400.00.

ILR School appreciates employees by providing the opportunity to pilot a nine day per month campus-to-home hybrid schedule.

No relocation assistance or visa sponsorship provided for this position.

Cornell appreciates employees with great rewards & benefits:

Cornell provides great benefits that include educational benefits, access to a plethora of wellness programs, employee discounts with local and national retail brands, health care options to choose from, generous paid leave provisions and superior retirement contributions.

Cornell has also been nationally recognized as an award-winning workplace for our health, wellbeing, sustainability, and diversity initiatives. For more information click here.

Familiarize yourself with Cornell's COVID-19 workplace guidance as well as the university's COVID-19 services and information.

University Job Title:

Job Family:

Level:

Pay Rate Type:

Pay Range:

Remote Option Availability:

Company:

Contact Name:

Job Titles and Pay Ranges:

Non-Union Positions

Noted pay ranges reflect the potential pay opportunity for each job profile. The hiring rate of pay for the successful candidate will be determined considering the following criteria:

• Prior relevant work or industry experience

• Education level to the extent education is relevant to the position

• Unique applicable skills

• Academic Discipline (faculty pay ranges reflects 9-month annual salary)

To learn more about Cornell’s non-union staff job titles and pay ranges, see Career Navigator.

Union Positions

The hiring rate of pay for the successful candidate will be determined in accordance with the rates in the respective collective bargaining agreement. To learn more about Cornell’s union wages, see Union Pay Rates.

Current Employees:

If you currently work at Cornell University, please exit this website and log in to Workday using your Net ID and password. Select the Career icon on your Home dashboard to view jobs at Cornell.

Online Submission Guidelines:

Most positions at Cornell will require you to apply online and submit both a resume/CV and cover letter.  You can upload documents either by “dragging and dropping” them into the dropbox or by using the “upload” icon on the application page. For more detailed instructions on how to apply to a job at Cornell, visit How We Hire on the HR website.

Employment Assistance:

For general questions about the position or the application process, please contact the Recruiter listed in the job posting or email mycareer@cornell.edu.

If you require an accommodation for a disability in order to complete an employment application or to participate in the recruiting process, you are encouraged to contact Cornell University's Office of Institutional Equity and Title IX at voice (607) 255-2242, or email at equity@cornell.edu.

Applicants that do not have internet access are encouraged to visit your local library, or local Department of Labor. You may also request an appointment to use a dedicated workstation in the Office of Talent Attraction and Recruitment, at the Ithaca campus, by emailing mycareer@cornell.edu.

Notice to Applicants:

Please read the required Notice to Applicants statement by clicking here. This notice contains important information about applying for a position at Cornell as well as some of your rights and responsibilities as an applicant.

EEO Statement:

Diversity and Inclusion are a part of Cornell University’s heritage. We are a recognized employer and educator valuing AA/EEO, and we do not tolerate discrimination based on any protected characteristic, including race, ethnic or national origin, citizenship and immigration status, color, sex/gender, pregnancy or pregnancy-related conditions, age, creed, religion, actual or perceived disability (including persons associated with such a person), arrest and/or conviction record, military or veteran status, sexual orientation, gender expression and/or identity, an individual’s genetic information, domestic violence victim status, familial status, marital status, or any other characteristic protected by applicable federal, state, or local law. We also recognize a lawful preference in employment practices for Native Americans living on or near Indian reservations in accordance with applicable law. 

Cornell University embraces diversity and seeks candidates who will contribute to a climate that supports students, faculty, and staff to all identities and backgrounds. We encourage individuals from underrepresented and/or marginalized identities to apply.

Job Description:

The Work Site Support Specialist is responsible for providing a work-based learning experience in a competitive integrated setting for eligible VR clients who are enrolled in high school. The Work Site Support Specialist will facilitate on-site support, as well as lead classroom discussion using ODEP’s soft skills curriculum for the development of employability skills in a real work environment. The Specialist completes necessary plans, reports and paperwork, as assigned.

Essential Job Functions:

• Coordinate students’ work-based learning experiences within the Pre-Employment Training - Work Experience Program with VR.
• Facilitate on-site support for students who will work a total of 16 hours at the identified worksite(s) over the course of four days within each week, with a target of 4 hours worked per day.
• During each 20-hour week of the program, the summer work employment specialist incorporates four hours of soft skills training per week and review/discuss on site experiences. This can be done at various times throughout each day, including at the beginning and end of each work shift.
• Support students on the worksite by facilitating individuals’ full integration into the
• worksite and serve as a mediator between co-workers and supervisors as necessary.
• Prepare plans, reports, and other paperwork as needed.
• Obtain information about student through intake process, including meetings with students and their families, VR Counselors, and school personnel in order to understand and know the student's strengths, skills, capacities, needs, vocational and other interests.
• Coordinate students’ new hire paperwork, orientation and weekly timesheets.
• Transports students to and from the worksite as needed.
• Reports worksite outcomes and other relevant information regarding progress/activity of student to Leadership and/or referral source as required.

Knowledge, Skills, and Abilities:

• Ability to read and interpret documents and write routine reports and correspondence.
• Ability to carry out instructions furnished in written, verbal or diagram form.
• Ability to deal courteously and effectively with co-workers, persons served, referral sources, and the business community.
• Ability to demonstrate patience and understanding of persons with disabilities.
• Ability to access and safely operate a vehicle.
• Ability to remain open-minded and empathetic to the needs of others.
• Ability to manage time well, prioritize, use good judgment, and work independently.
• Ability to speak effectively before groups.
• Good oral and written communication skills.
• Abide by the policies and procedures regarding confidentiality, professional ethics, and codes of conduct.
• Maintain a positive attitude in the work environment.
• Computer and data input skills

Experience and Education Qualifications:

• High School Diploma or GED required.
• Preferably has experience in employment services, job coaching, business, sales, human resource or human services.

Supervisory Requirements:

• None

Employment Requirements:

• Successful completion of background check including criminal record, driving record and abuse/neglect.
• Completion of New Hire Orientation at the beginning of employment.
• All training requirements including Relias at the beginning of employment and annually thereafter.
• Must have and maintain certification in CPR, First Aid, and Blood borne Pathogens.
• Must have a valid driver's license, acceptable driving record and current auto insurance.

Physical Requirements:

The physical demands described here are representative of those that must be met by an associate to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

While performing the duties of this job, the associate is regularly required to talk or hear. The associate is frequently required to stand and walk. The associate is occasionally required to sit. Specific vision abilities required by this job include close vision, distance vision, peripheral vision, depth perception, and ability to adjust focus.

We are an Equal Opportunity and Affirmative Action Employer, and encourage applications from all qualified individuals without regard to race, color, religion, sex, gender identity, gender expression, sexual orientation, national origin, age, marital status, disability or veteran status, or to other non-work related factors.

Supported Living and Employment Services is a Smoke and Tobacco Free Workplace.

• The Medical Scientific Liaison (MSL) will be in charge of delivering updated scientific information to a broader group of healthcare professionals.
• The role of the Medical Scientific Liaison will be to provide essential information which in most instances  will be medical, but it can also be purely technical linked to other fields such as biology, pharmacoeconomic data, pharmacology, etcetera, with personal contact, visiting key physicians locally and around all the country, in fact, the main activities will be in a field work setting.
• The Medical Scientific Liaison will have a constant cross functional interaction with different members of the Business Unit.  The top priority of a MSL is to provide scientific information to health care providers and obtain insights. MSL will actively engage in activities that support the strategic direction of a product. Therefore, MSL will be exposed to key decision makers both within the organization and outside the company. As catalysts of collaboration between Pfizer and HCP, MSL will be a key player to transmit updated scientific information, research resources and business intelligence.
• Provide scientific information to HCPs involved in the specific Pfizer drugs to increase the knowledge about disease, its diagnosis and drug efficacy, safety and correct use.
• Need to be aware of the latest medical/scientific information with regards to the therapeutic area under his responsibility.
• Develop and maintain professional relationships with KOLs and academic centers to ensure their access to current medical and scientific information
• Develop specialized rising stars and opinion leaders, to become KOLs, clinical investigators and/or speakers. 
• Prepare and develop the scientific information and materials to be discussed with the HCPs with the support advice and approval of the Medical Manager.
• Coordinate medical events as part of the objectives in diffusion of scientific information.
• Participate in medical educational programs and disseminate technical information regarding the product and disease concepts, identifying competitive advantages or potential new uses of the target Pfizer product.
• Work with the Medical Manager to partner with stakeholders to identify opportunities for the development of treatment algorithms and guidelines.
• Collaborate with Medical Manager to facilitate identification and presentation of research opportunities for consideration in support of the product and customers.
•  Assist in implementation of local protocol development and administration for proposals to be supported.
• Provide information to local experts to assist in keeping their presentations current and ensure they have medical and scientific information necessary when responding to questions encountered during their presentations
• Support on-going training to field sales force, personnel and others, providing up-to-date knowledge of the product uses and external data.
• Serve as local medical scientific resource planning for communication of product information.
• Attend scientific meetings, review scientific journals and partners with Category Leads and Medical Managers to foster information on medical concepts and product usage.
• Act in compliance with all Pfizer policies and particularly with FCPA, GPIHP and PIGO policies
• To provide reports and metrics (if required by Manager) supporting results aligned with medical objectives.
• If required by manager, provide administrative support in ISRs.

REQUIRED SKILL SET

Technical

• Microsoft Office management
• English proficient
• Scientific acumen

Managerial

• Objective oriented
• Audience management
• Training and efficient communication
• Analytic and proactive
• Self-study discipline

Education

• Medical degree, preferable with specialty in Internal Medicine and/or research or molecular biology training.

Experience

• +2 years of Experience as MSL or specialized physician, and/or at least 1 year in the pharmaceutical industry, mainly in contact with Medical societies of interest, in continuous interaction and scientific exchange.

EEO (Equal Employment Opportunity) & Employment Eligibility 

Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, or disability.

About the role

As our next Program Officer, you will contribute to the Impact & Sustainability team in creating as well as managing environmental, social, and governance initiatives in Amartha.

Responsibilities

• Report Writing Assistance
• Planning, executing, and monitoring social impact projects.
• Developing project plans, timelines, and tracking project progress.
• Collaborate with team members to ensure project efficiency.
•  Data Analysis and Reporting
• Assist in collecting and analyzing data related to project outcomes.
• Support in preparing impact report
• Administration
• Assist with administrative tasks such as document/payment processing and procurement.

The qualifications that you must have

• open for fresh graduate (from relevant social sciences field such as sociology, psychology, social welfare, public health, anthropology, public administration, etc)
• Good verbal and written english skills
• Strong interest in social work and socially impactful projects.
• Good communication and interpersonal skills.
• Motivation to learn and grow in a real-world work environment.
• Attention to details and willingness to learn project management tools

Current Employees:

If you are a current employee, please apply via the internal career site by logging into your Workday Account and clicking the "Career" icon on your homepage.

Starting Pay Rate Range

to

(Determined by the knowledge, skills, and experience of the applicant.)

Job Summary

Monument Health offers competitive wages and benefits on qualifying positions. Some of those benefits can include:

*Supportive work culture

*Medical, Vision and Dental Coverage

*Retirement Plans, Health Savings Account, and Flexible Spending Account

*Instant pay is available for qualifying positions

*Paid Time Off Accrual Bank

*Opportunities for growth and advancement

*Tuition assistance/reimbursement

*Excellent pay differentials on qualifying positions (extra pay for working evening, nights or weekends)

*Flexible scheduling

Job Description

Essential Functions:

• Assist lead CRC in developing source document templates in Microsoft Word, Excel, or similar program. Source documents should be routinely maintained to reflect accurate information that is required of sponsors by verifying against eCRF software.
• Completes relevant data collection, entry and analysis as and when needed.
• Coordinates the efforts of case finding and recruitment of study patients.
• Create, organize, submit, and maintain all pertinent study documents, records, and logs from start-up to study closure between sponsor and other offices. Documents would include regulatory documents, contracts, temperature logs, budgets, licenses, training documentation, etc.
• Creates and maintains study and subject specific case report forms. Develop data collection worksheets that ensure complete collection of data which can be accurately transmitted by data entry staff.
• Demonstrates the ability to work in collaboration with other members of the Clinical Research Team to provide safe quality care to our subject population and efficiently complete daily responsibilities which include the following:
• Develop documents and processes for successful trial implementation which are consistent with internal processes and procedures, regulatory requirements, and “Good Clinical Practice.”
• Facilitate site monitoring visits by assuring they have all the information and materials needed to effectively perform their job, assisting them while on site, close-out visit with investigator, addressing action items in monitoring letter.
• Follows study protocol in scheduling of tests, procedures, and administration of medications.
• Implement effective study-specific screening, enrollment, and follow-up processes.
• All other duties as assigned.

Additional Requirements

Preferred:
Experience - 1+ years of Clinical Research Experience
Education - Associates degree in Health Related Field
Certification - Clinical Research Coordinator Certification - Accredited University or accredited training professionals

Job Category

Job Family

Department

Scheduled Weekly Hours

Shift

Employee Type

Make a difference.  Every day.

Monument Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, or protected Veteran status.

This is a fully on-site position at our Salt Lake City, Utah location.

Overview:

This individual will play a key role in assisting in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include logical thinking, ability to prioritize, “can-do” attitude, the ability to adapt quickly to changing business conditions, strong interpersonal and team building skills. The employee, working closely with study team members, will achieve study objectives and corporate goals. 

Essential Functions

• Ability to coordinate as primary CRC on at least 1-3 studies of low to medium complexity, with oversight by a manager or higher-level CRC. 

• May assist as back-up CRC on other studies

• Develops and implements patient recruitment strategies; actively recruits to ensure enrollment targets are achieved

• Obtains informed consent of research subjects

• Develops strong working relationships and maintain effective communication with study team members

• Completes all protocol related training

• Performs patient/research participant scheduling

• Collects patient/research participant history 

• Collects and maintains source documentation

• Manages inventory and administers test articles/investigational product to participants 

• Performs data entry and query resolution

• Supports the collection and review of required essential study documents and reports. Order supportive study supplies (e.g., contracts, IXRS, lab kits, nonclinical supply materials, imaging, and laboratory handling manuals, etc.)

• Adheres to an IRB approved protocol

• Supports the safety of research subjects, report adverse events

• Coordinates protocol related research procedures, study visits, and follow-up 

• Facilitates pre-study, site qualification, study initiation, monitoring visits, and study close out activities

• Collects, processes and ships laboratory specimens

• May be asked to perform special project responsibilities and travel to other clinic locations, within the area, when needs arise

• Complies with Avacare and Sponsor policies, standard operating procedures (SOPs) and guidelines

• Performs other duties as assigned

Qualifications

• Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines

• Clinical Research Coordinator experience within a similar setting preferred

• Clinical skills experience including obtaining vitals, phlebotomy, EKG, etc. preferred

• Knowledge and experience of site operations and the drug development process

• Effective communication

• Computer proficiency in use of Microsoft Word, Excel

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe

IQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status. https://jobs.iqvia.com/covid-19-vaccine-status