Position: Clinical Research Cord./Research Assistant 3

Location: Community Dentistry - School Of Dentistry, Cleveland, OH 44107

Duration: 12 Months

Pay-Rate: $19/Hr. on W2

Essential functions:

• Coordinate and carry out all research activities including devising new procedures and techniques for scheduling, tracking, and completing study activities in preparation for and during the clinical trial. These activities include subject recruitment, collection of qualitative and quantitative study data, and data analysis. (35%)
• Work closely with the principal investigator, research operations manager and research associate to devise, implement and ensure compliance with study protocols. Devise new protocols and techniques for scheduling, tracking, collecting data and completing subject visits as per the newly developed study protocols. (15%)
• Carry out complex research assignments of a non-routine nature to evaluate adequacy of techniques to collect data. Study and test new procedures for entry of participant responses into the database, audit entered data and perform quality control to ensure that data is entered completely and correctly. Oversee analysis of recruitment data to ensure compliance with inclusion/exclusion criteria and study protocol. (15%)
• Communicate with assigned study site staff to resolve issues and communicate daily schedules and subject recruitment and study visit logistics. (10%)
• Build and establish relationships with participants, MetroHealth Medical Center providers and medical staff to ensure successful completion of study objectives. (6%)

Nonessential functions:

• Develop training materials and train new staff or students. (5%)
• Co-author, develop and maintain the protocol, manual of procedures (MOP), training manuals and regulatory documents for the study. (5%)
• Develop and compile summary data for weekly project meetings, progress reports, IRB submissions, presentations and manuscript submissions. (5%)
• Perform other duties as assigned. (4%)

Contacts:

• Department: Daily interaction with research assistants and the principal investigator. Monthly interaction with department administrative staff to exchange information
• University: Occasional interaction with co-investigators to exchange information.
• External: Daily contact with older adult participants for study visit completion, and through phone contact for retention purposes. Weekly contact with MetroHealth Medical Center personnel for recruitment purposes and study visit completion.
• Students: Occasional interaction with student workers to exchange information.

Supervisory responsibility:

• No direct supervisory responsibility.

Qualifications:

• Experience: 3 to 5 years of experience is required. Previous experience working with older adults is preferred.
• Education/Licensing: Bachelor s degree in clinical science, social science, epidemiology or related field required. Master s degree preferred. Valid Ohio driver s license required.

Required skills:

• Considerable knowledge and understanding of commonly-used concepts, practices and procedures within the field of clinical research.
• Exceptional interviewing skills: ability to work with sensitive patient information and maintain confidentiality. Must demonstrate an understanding of human subject protections and diligently seek to promote such protections and follow all human subject regulations.
• Ability to effectively interact with older adults. Must demonstrate patience, flexibility, compassion and cultural sensitivity while interacting with participant families.
• Excellent organizational skills. Ability to multi-task, prioritize and meet deadlines. Must demonstrate attention to detail and accuracy, time management skills, and follow-through.
• Excellent communication skills. Must demonstrate the ability to effectively and professionally communicate and work with various individuals from different disciplines, technical and educational backgrounds.
• Effective problem-solving skills. Must demonstrate sound Judgement and good decision-making and be able to flexibly work to conform to shifting priorities and demands and high pressure situations.
• Excellent leadership skills. Must be able to oversee people, multiple ongoing project activities and appropriately provide feedback to others when needed.
• Ability to follow directions and standardized protocols and demonstrate diligence and dependability. Must demonstrate ability to receive and accept feedback from supervisors, put feedback into practice, and work both independently and cooperatively.
• Ability to effectively interact with colleagues, supervisors and participants face to face.
• Ability to meet consistent attendance.

Working conditions:

Employee will be required to drive to MetroHealth Medical Center clinical sites to collect research data. A valid Ohio driver s license and reliable transportation is required. The research assistant will work in a general office environment for other research activities.

Job Types: Full-time, Contract

Pay: $19.00 per hour

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Vision insurance

Schedule:

• 8 hour shift
• Day shift
• Monday to Friday

Application Question(s):

• Have you been Vaccinated? If No, Are you willing to get Vaccinated before the start?
• Your Email Address, Contact Number and, the Best Time to reach you?

Experience:

• Clinical research: 3 years (Preferred)

License/Certification:

• Ohio driver s license Location: One location

Sr Clinical Research Assistant

Lifespan

East Providence, Rhode Island



Summary

Under general supervision, but following established policies and procedures, performs scientific investigative research in areas related to patient care. Research literature in the field, participates in the design of experimental protocols and develops new procedures to carry out established research objectives. Interviews patients to gather information, prepares and maintains study record, enters data via computer, performs statistical analyses of resultant data. Participates in the qualitative/quantitative analyses of data. May assist in writing presentations and papers for publication based on the research performed. May perform EKG’s and take vital signs during research-based monitoring tests. May also perform blood spinning and shipment of blood and tissue samples as required by protocol.



Responsibilities:

· Identifies patients meeting criteria for inclusion in clinical research studies, ensuring research protocol eligibility requirements are met.

· In collaboration with the research investigator, participates in the design of experimental protocols to achieve the scientific objectives of the research project.

· Develops research methodologies within the parameters of experimental protocols and research objectives to allow quantitative and qualitative evaluation and interpretation of data obtained.

· Establishes and maintains study record for each participant. Interviews patient and/or family to explain the nature of the study, eliciting cooperation and gathering information to complete study questionnaire. Facilitates obtaining informed consent. May assist to schedule patient appointments and make calls to patients to complete documentation.

· Reviews medical records to abstract information necessary to complete forms. Requests and follows up on missing data such as laboratory test results and the like.

· Regularly monitors adherence to protocol; alerts physician when laboratory tests ordered have not been performed, medication protocol not followed, etc.

· Collects and organizes patient data into appropriate format to facilitate data entry. Creates, modifies as appropriate and maintains study database to meet needs for project. Gathers, tabulates, graphs develop explanatory charts, and analyzes data using statistical methodology. Performs computer-assisted statistical analysis such as multiple antecedent variables, linear regression, frequencies, cross-tabulation and the like. Writes non-complex programs using computer and software-compatible language to reformat information, create new files, etc.

· Prepares and maintains related graphs and charts or results of data gathered. Participates in quantitative/qualitative analyses of resultant information.

· May provide functional guidance to subordinate research staff assigned to the project to provide clarification of protocol, resolve issues, ensure adherence to research protocol procedures and assist in developing their professional skills in reviewing and interpreting statistical trends and the like.

· Participates in the interpretation of the results of experiences through conferences with principal investigator and other research professionals involved in the study to review data compared to hypothesis and research methodology in instances of inexplicable data. May make recommendation for modification of research protocol based upon initial findings.

· May assist in writing presentations and papers for publications based on research performed.

· Regularly reviews relevant literature to research being conducted in order to better understand the project. Maintains and enhances professional expertise through educational opportunities and participation in related teams and conferences.

· May perform research-based EKG’s, vital signs, blood spinning and shipping of blood and tissue products, in accordance with protocol specifications.


Basic Knowledge:

· Bachelor’s Degree in Biological Sciences with 2 - 3 years progressively more responsible related experience.

· Requires a working knowledge of statistics, computer programming and research methodology.

· Requires an in-depth knowledge of the scientific field in which the research is being conducted.



Experience:

· Two to three years’ experience in the particular research field.



Work Environment:

· Completion in a laboratory environment with possible exposure to human and animal serum chemical reagents, animal subjects and radioactive materials.



Independent Action:

· Performs independently within the department’s policies and practices. Refers specific complex problems to the supervisor when clarification of the departmental policies and procedures are required.



*Working at Lifespan

At Lifespan, we utilize a multidisciplinary team approach to medicine and provide the right blend of autonomy and collaboration. If you share our passion for providing the very best care in a supportive professional setting, join one of the nation’s Top 100 health systems. Consistently awarded Magnet® status in nursing care, Lifespan is committed to clinical excellence and devoted to our mission of delivering health with care.



Job ID: 58891

Lifespan is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, ethnicity, sexual preference or orientation, ancestry, genetics, gender identity or expression, disability, protected veteran or marital status. Lifespan is a Vevraa Federal Contractor.

Job Type: Full-time

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Paid time off
• Vision Location: In person

Join our remarkable team!

The Neurology Center of New England is a comprehensive neurological care center devoted to the diagnosis, care and management of patients with neurological diseases and syndromes.

We are currently hiring a motivated Clinical Research Assistant for a full time position.

In this position, you will conduct daily operations of clinical research trials focusing on the treatment of Multiple Sclerosis, Parkinsons's disease, Alzheimer's disease and other neurological conditions.

Qualifications:

• Prior experience in a research environment or equivalent combination of education and experience in a health-related field
• Outstanding interpersonal skills
• Careful attention to detail
• Ability to prioritize a variety of tasks and properly manage time between multiple clinical study-related tasks
• A positive attitude and willingness to learn
• Exceptional problem-solving and organizational skills
• Phlebotomy skills preferred, but not required

Responsibilities:

• Provide assistance on multicenter, pharmaceutical-sponsored clinical research studies as per study guidelines and protocols
• Recruit and enroll subjects into clinical trials focusing on the treatment of Multiple Sclerosis, Parkinsons disease, Alzheimer's disease, and other neurological conditions
• Respond to phone calls or inquiries regarding study protocol. Refer qualifying candidates to clincial staff when appropriate
• Create and complete detailed subject case report forms and enter source data into electronic datatbases
• Maintain accurate, organized and detailed records of study participant and investigator site files
• Coordinate subjects' study appointments according to visit window as specified in individual study protocols
• Assist with various clinical tasks such as questionnaire administration, collection of vital signs, ECG administration, processing and shipment of blood specimens
• Ensure that all non-serious and serious adverse events are properly documented and promptly reported
• Adhere to good clinical practice standards and study protocols
• All other duties, as assigned

Job Type: Full-time

Pay: $16.00 - $19.00 per hour

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Employee assistance program
• Health insurance
• Paid time off

Schedule:

• 8 hour shift
• Day shift
• Monday to Location: In person

About Testing Done Simple:
Testing Done Simple is a startup company trying to make diagnostic testing easier for people. We bring easy to use solutions for the most important health issues. We are innovative, professional, and bring high quality products to patients and people. We are conducting a clinical trial and need a Covid testing technician to join our team.

Responsibilities:
Screen patients by asking a series of questions
Obtain medical history of potential research subjects
Present informed consent form to subject
Administer nasal swab

Record covid test result
Answer patient's questions or concerns

Adhere to HIPAA guidelines
Consults principal investigator
Follow safety and infection control standards

Seeking a Registered Nurse

Qualifications:
CRN
Direct patient care experience preferred

Part-time

Astoria

Job Types: Part-time, Contract, Temporary

Pay: $35.00 - $37.00 per hour

Schedule:

• Day shift

Ability to commute/relocate:

• Brooklyn, NY 11216: Reliably commute or planning to relocate before starting work (Required)

Application Question(s):

• Do you have experience performing Covid nasal swab tests?
• Do you have any research experience?
• Have any medical malpractice claims ever been made against you?
• Will you be okay completing a 2 hour online research course?

Education:

• Bachelor's (Required)

Experience:

• Patient care: 1 year (Required)

Language:

• English (Required)
• Spanish (Preferred)

License/Certification:

• CRN (Required)

Shift availability:

• Day Shift Location: One location

The Roskamp Institute, Inc., is a vibrant biomedical research organization in Sarasota, FL, that is focused on understanding and developing cures for neurodegenerative diseases including Alzheimer s Disease and traumatic brain injury and neurological illnesses caused by environmental exposures. It is multifaceted, incorporating Ph.D. education, basic and clinical research. The successful candidate will work under the direction of senior scientific staff to assist in carrying out research studies in a team setting. The Roskamp Institute provides a strong comprehensive compensation package.

Position Summary: This position will work mainly at the Sarasota location but may be asked to assist other data collection sites in the Tampa, St. Petersburg, or Lakeland areas on occasion. This position will assist with a large randomized clinical trial and will perform job duties including, but not limited to, administering computerized brain training exercises to older adults, maintaining communication to monitor participant progress in their training exercises, obtaining informed consent, administering neuropsychiatric assessments, data quality control, and recruitment and retention efforts. This position supports the Cognitive Aging Lab within the USF Department of Psychiatry and Behavioral Neurosciences.

Responsibilities:Collects, analyzes, and enters data for clinical trials and ensures quality control. Administers study activities according to the study protocol. Establishes rapport with study participants and maintains contact with participants enrolled in the study. Facilitates, supports, and motivates older adult study participants during their study participation. Communicates by email and phone with study participants to ensure adherence to intervention. This position will work mainly at the Sarasota location. Participates in the mandatory weekly lab meeting. Implements study participant recruiting and screening protocols. Meets recruitment and enrollment goals. Determines if older adult participants meet study eligibility requirements. Obtains informed consent from older adult study participants. Devotes at least 5 hours weekly to telephone recruitment and interviewing. Completes data forms with high accuracy and attention to detail. Travels to and attends community events to assist with recruitment and facilitate meeting enrollment goals including diversity goals. Disseminates information on studies to study participants and the general public. Ensures that documents such as eligibility forms and informed consent are appropriately gathered and maintained, and IRB-, Good Clinical Practice-, and HIPAA regulations are followed. Trains any assistants and volunteers who gather and enter data. Monitors compliance of study procedures with federal, state and university regulations. Performs data quality control procedures to ensure clean and accurate data. Work with minimal supervision, plans, organizes, and coordinates multiple work assignments and establishes and maintains effective working relationships with others. Effectively and professionally communicates sensitive information and maintains confidentiality. Performs other duties as assigned.

Position Qualifications:

• B.S or B.A. degree in biological or clinical sciences preferred.
• Excellent verbal & written communication skills
• Self-organizing & presentation skills
• Excellent interaction skills
• Computer competency

Preferred:

• Bilingual proficiency in Spanish and English
• Prior research experience

Job Type: Full-time

Pay: $38,000.00 - $47,000.00 per year

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Flexible schedule
• Flexible spending account
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Vision insurance

Schedule:

• 8 hour shift

Ability to commute/relocate:

• Sarasota, FL 34243: Reliably commute or planning to relocate before starting work (Required)

Experience:

• Clinical trials: 1 year (Preferred)
• Research: 1 year Location: In person

Company description:

NuFargo Global Inc. is a US-based company dedicated to the research and development, clinical testing, manufacturing and distribution of high-quality natural health and wellness products.

Responsibilities:

We are seeking an experienced Clinical Research Associate to join our team and participate in all research activities for new type of health care products while under the direction of the team leaders, investigators, Financial Administrative Office, Faculty Director, Medical Director, and Senior Research Director. You will be responsible for completing the data management of clinical research studies and for collection and transcription of research patient data and study related information into research records and assist with maintenance of regulatory files to fulfill research requirements. In this role you will work with study monitors to process and collect accurate data in a timely manner and assist investigators and study coordinators in clinic settings.

Work may be assigned by the team leader, investigator or Administration, and assignments may be changed on an as-needed basis in order to ensure that studies and patient care needs are handled appropriately and in a timely manner.
Required:

• Demonstrated working knowledge of current medical terminology specific to pharmacology, to accurately read entries in patient charts and record accurately and timely, information into study records and other appropriate research data forms.
• Clinical research experience, with in depth knowledge of clinical pharmacology as it pertains to clinical trials and studies.
• Demonstrated organizational skills to efficiently and effectively provide data management/monitoring support for multiple clinical trials and projects, providing accurate information in a timely manner.
• Bilingual in Chinese and English
• Major in Bio-Chem, chem, or biology.

Job Type: Full-time

Pay: From $5,500.00 per month

Benefits:

• Health insurance
• Paid time off

Schedule:

• 8 hour shift

Application Question(s):

• Were you major in Bio-Chem?

Education:

• Bachelor's (Required)

Experience:

• Clinical research: 1 year (Preferred)

Language:

• Chinese Location: One location

General Summary OF Position:

Under the supervision of the Principal Investigator or designee, the Clinical Research Assistant is responsible for performing delegated tasks and procedures involving human subjects in support of clinical research protocols.

MAJOR Responsibilities:

• Assist PI in development of protocol-specific tools to aid in study documentation
• Assess eligibility of research subjects in accordance with the approved protocol and all applicable regulations including HIPAA
• Obtain patient consent and Human Subject Committee approvals for minimal-risk studies as delegated by IRB-approved protocol
• Collect, record, evaluate, update, and store/transport pertinent data and samples in relation to protocol
• Track study enrollment and completion of milestones
• Summarize research findings and prepare presentations
• Perform literature searches
• Schedule patient tests and/or interviews
• Conduct patient telephone follow up
• Stock, inventory, store, and order samples/supplies as needed to maintain appropriate operations
• Review medical records and medical record abstractions for consistency and completeness
• Comply with established policies, health and safety regulations and requirements, procedures, and department objectives
• Maintain patient and study subject confidentiality
• Perform other duties as required.

Required Qualifications:

• Bachelor's degree in a scientific or health care field, or related experience
• Experience in using computer-based tools (Word, Excel, Access, Outlook, PowerPoint, etc.)
• Oral and written communication skills
• Excellent organizational and interpersonal skills required.

Job Type: Full-time

Benefits:

• Dental insurance
• Health insurance
• Paid time off
• Vision insurance

Schedule:

• 8 hour shift

Ability to commute/relocate:

• Worcester, MA 01655: Reliably commute or planning to relocate before starting work Location: One location

Clinical Research Assistant

About Center For Sight:
Center For Sight is one of the nation's leading multi-specialty physician groups providing patients worldwide with care in ophthalmology, optometry, dermatology and cosmetic facial surgery. With fourteen locations based in Florida, over 60 providers, and 600 team members system wide, Center For Sight is the largest practice in Southwest Florida, managing over 100,000 patient visits per year.

Providing an outstanding patient experience is extremely important to our team and our efforts have led us to be recognized as the practice of choice in Southwest Florida by local residents in the Sarasota Herald Tribune Readers' Choice Awards, year after year. We are proud to be named the #1 practice in the area; an honor that wouldn't be possible without employing the best and brightest team members to help us deliver world class patient service. We believe in hiring right and providing our team with ample opportunities for advancement and training. We invite you to explore our open opportunities and learn more about our practice.

About the Area: Sarasota
Sarasotans agree there is a reason our home has been included in the top 50 Best Places to Live by U.S. News, named one of the South's Best Cities by Southern Living and recognized as one of the Top 25 Most Desirable Places to Live by MSN Money. Sarasota offers amenities to suit any taste or interest, from unique cultural attractions to fine dining and unrivaled outdoor activities for families to enjoy.

Siesta Key Beach has been named the #1 Beach in the USA and the city is the 10th fastest growing metropolitan area in the nation according to the U.S. Census Bureau. In addition, the Sarasota County school system is one of the highest ranked in Florida, which is also home to Pine View, a gifted magnet school continually ranked as the #1 high school in the state. With its beautiful beaches, no state income tax, and rapidly growing population, Sarasota provides an idyllic opportunity to live and work in paradise.

Job Summary:
The Clinical Research Assistant works alongside Study Coordinators to conduct clinical work ups which include, but are not limited to: collecting blood draws, vitals, lens refraction, intraocular pressure measurements and pachymetry. The Clinical Research Assistant will also be responsible for data entry, scheduling appointments and calibrating laboratory equipment. This individual will coordinate and participate in clinical research studies conducted by investigators at Center For Sight using Good Clinical Practice.

Travel to multiple locations is required.

Benefits:
We offer a competitive benefits package, which includes: health, life, disability and dental insurance, matching 401K plan, paternity leave, generous vacation and holiday pay, and many employee discounts

Drug and Smoke Free Type: Full-time

Join the HJF Team!

The Henry M. Jackson Foundation for the Advancement of Military Medicine (HJF) is a nonprofit organization dedicated to advancing military medicine. We serve military, medical, academic and government clients by administering, managing and supporting preeminent scientific programs that benefit members of the armed forces and civilians alike. Since its founding in 1983, HJF has served as a vital link between the military medical community and its federal and private partners. HJF's support and administrative capabilities allow military medical researchers and clinicians to maintain their scientific focus and accomplish their research goals.

This position will be in support of the Military HIV Research Program (MHRP). The incumbent is responsible for research and/or development in collaboration with other scientific and technical staff and provides laboratory and technical support to senior technical and professional staff. Work will involve contemporary and emerging technologies to analyze humoral cell immunology in the state-of-the-art laboratories at MHRP. Work will also involve developing experiments with new tools in cellular biology, immunology and virology, to collect, analyze, and communicate data. Studies will involve expertise in enzyme-linked immunosorbent assay, tissue culture, virus growth and purification , flow cytometry, and HIV- I infection assays.

[website]

Responsibilities

HJF is seeking a Research Assistant II to perform research and/or development in collaboration with others for projects. The Research Assistant provides laboratory and technical support to senior technical and professional staff and solves problems of standard complexity in carrying out research projects in a clinical or laboratory environment.

Responsibilities

• Maintains compliance with established laboratory safety and other procedures.
• Ensures the proper disposal of infectious and hazardous materials.
• Applies quality control measures as outlined/required by the protocol. Provides basic data analysis.
• Performs laboratory research projects, including collection and organization of data, and maintaining databases. Makes detailed observations on experiments.
• Assists in the preparation of reports, publications, and presentations.
• Follows instructions and standard operating procedures to perform expected tasks. May provide basic instruction to other lab staff.
• May perform other duties and responsibilities as assigned or directed by the supervisor. This may include attendance of and participation in required training for role.

Required Knowledge, Skills and Abilities

• Knowledge of standard laboratory and immunological techniques.
• Knowledge of ELISA, PCR, DNA/RNA isolation, and gel electrophoresis.
• Ability to follow detailed instructions.
• Good communication and analytical skills.
• Basic computer skills
• Ability to meet project deadlines.

Physical Capabilities

• Lifting: Requires lifting materials up to 8 lbs.

Qualifications

Work Environment

• This position will take place primarily in a laboratory setting.

Education and Experience

• Bachelor's Degree required, Master's degree preferred
• Minimum of 3-5 years experience required

As per Executive Order 14042, all HJF employees are required to be fully vaccinated against COVID-19. Proof of vaccination or an approved religious or medical accommodation will be required.

Employment with HJF is contingent upon successful completion of a background check, which may include, but is not limited to, contacting your professional references, verification of previous employment, education and credentials, a criminal background check, and a department of motor vehicle (DMV) check if applicable. Any qualifications to be considered as equivalents, in lieu of stated minimums, require the prior approval of the Chief Human Resources Officer.

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities

The contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information. 41 CFR 60-1.35(c)

Job Type: Full-time

Benefits:

• 401(k)
• Dental insurance
• Flexible schedule
• Health insurance
• Paid time off

Schedule:

• 8 hour Location: One location