60 Medical Assistants jobs in Newark

Medical Technologist Positions Outside Columbus Ohio!

Work for a Top Healthcare System in the State.

Known for Commitment to Health and Well-Being of Employees

• Multiple openings
• Various shifts-mostly 2nd and 3rd (Sign on bonus + Shift Differential)
• Perform moderate and high complexity testing in some or all areas of the lab including Chemistry, Hematology, Microbiology, Serology, and Blood Bank.
• Key responsibilities: proper patient and specimen identification, adhere to testing policies and procedures, instrument use and troubleshooting.
• Hospital has been recognized for its commitment to the health and well-being of its employee

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. **Position Overview:** The Medical Director will be responsible for clinical strategy relating to upcoming clinical trials, including indication selection, design of trials, and ongoing medical monitoring of safety signals in trials. This is a remote role and candidate can be located anywhere within the US. **Responsibilities include, but are not limited to the following:** + Design of trials, including study population and eligibility criteria, treatment duration, clinical endpoints, biomarkers, and safety mitigation strategy + Serve as the Program Physician for associated clinical trials, addressing patient eligibility and treatment questions in collaboration with the contract research organization (CRO) medical monitor, or directly with study investigators + Work closely with preclinical scientists to understand how the biological effects observed in animals can be translated to humans, and use this information to choose the best clinical endpoints and biomarkers for clinical trials + Be familiar with the nonclinical safety data (toxicology) and use this information to develop safety mitigation strategies in clinical trial design + Serve as a key part of the cross-functional project team, supporting the overall strategy, budget, and timeline of the project + Review safety data for individual subjects and trend review for safety signals from ongoing trials + Interpret, summarize, and present data from clinical trials to the company and externally + Provide strategic input for clinical development plans and regulatory strategy + Provide input/review of clinical documents, e.g. protocols, investigator's brochures, case report forms + Participate in site/investigator identification and evaluation for clinical trials; conduct site engagement calls and visits + Lead preparation of clinical sections of relevant regulatory filings (IND, study reports, NDA, etc.) in cooperation with colleagues in Regulatory Affairs and other functions + Serve as program medical expert for internal and external collaborators, investigators, consultants, and contract resources + Provide and enhance knowledge in the associated therapeutic area to support global clinical development plans + Represent the company at scientific meetings and presentations + Attend and provide medical support for investigator and consultant meetings and clinical advisory boards + Develop and manage relationships with key opinion leaders to obtain advice and feedback **Skills/Qualifications/Education Requirements:** (To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions) + Medical Degree + Typically requires 8 years of clinical research experience with at least 5 years of clinical document production and/or clinical trial feasibility and strategy or related experience. Additional experience may include other pharmaceutical or academic research in the field. + Hands-on experience with clinical trial design, trial conduct and oversight, including medical monitoring for trials in a broad spectrum of indications including medical immunology, hematology, and oncology. + Knowledgeable in GCP guidelines in US and Europe + Team player with good oral presentation and written skills + Collaborative and flexible in personal interactions + Ability to work proactively and effectively, with exceptional problem-solving skills + Up to 25% travel _*Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements. Example: If a job level requires a Bachelor's degree plus 4 years of experience, an equivalency could include 8 years of experience, an Associate's degree with 6 years of experience, or a Master's degree with 2 years of experience._ If you have the work ethic and mental agility to embrace a fast-paced and rapidly evolving environment, you will be rewarded with diverse and exciting experiences. This is your chance to add real value to an entrepreneurial organization that supports bold innovation and new ideas. Grifols welcomes passionate, team-oriented colleagues who are looking to improve the health of patients worldwide by developing a deeper understanding of human disease. **Pay Scale:** The estimated pay scale for the Medical Director (1-2) role based in the United States (non-California), is $170,000.00 - $40,000.00 per year/per hour. Additionally, the position is eligible to participate in 15% - 30% of the company bonus pool (depending on level of role). We offer a wide variety of benefits including, but not limited to: Medical, Dental, Vision, PTO, 9 paid Holidays per year, up to 5% 401(K) match and tuition reimbursement. Final compensation packages will ultimately depend on education, experience, skillset, knowledge, where the role is performed, internal equity and market data. We are committed to offering our employees opportunities for professional growth and career progression. Grifols is a global healthcare organization with employees in 30 countries focused on patient health and providing impactful results. Since our humble beginnings in 1909, Grifols has been a family company that prides itself on its family-like culture. Our company has more than tripled over the last 10 years, and you can grow with us! **For Washington State:** Currently, the first year PTO accrual for this role is 160 hours per year. Then, after completion of 365 days of employment the PTO accrual for this role will increase to 180 hours per year. **For California:** The estimated pay scale for the Medical Director (1-2) role based in California, is 170,000.00- 250,000.00 per year. Work is performed in an office environment with exposure to electrical office equipment. Frequently sits for 6-8 hours per day. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists. Occasionally walks and stands. Occasionally bends and twists neck. Light to moderate lifting and carrying objects with a maximum lift of 25lbs. Frequently drives to site locations with occasional travel within the United States. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken and written words and sentences. Interacts with others, relates sensitive information to diverse groups. Must work with diverse groups to obtain consensus on issues. Third Party Agency and Recruiter Notice: Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate. **Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws, including but not limited to, the California Fair Chance Act, the Los Angeles County Fair Chance Ordinance for Employers, and the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.** Learn more about Grifols ( **Req ID:** 528005 **Type:** Regular Full-Time **Job Category:** Clinical Trials

Medical Technologist / Medical Laboratory Technician - ASCPThis leading healthcare provider situated in Newark, OH and Gratiot, OH is seeking a dedicated Medical Technologist or Medical Laboratory Technician to join their advanced laboratory team. This is a chance to contribute significantly in a high-stakes environment that performs over 1.8 million tests annually. If you're a motivated individual looking to push forward your career in a state-of-the-art facility, we offer numerous career growth opportunities, competitive salary, and a comprehensive benefits package. This position allows you to harmoniously blend professional rigor with the serene lifestyle offered by our rural setting, while still having close access to urban amenities.Salary: $23.50 - $38.90 per hourEssential Duties and Responsibilities: Conduct clinical laboratory tests in the fields of hematology, chemistry, microbiology, immunology, and clinical microscopy. Obtain and analyze specimens effectively while maintaining data integrity and confidentiality. Utilize and maintain laboratory equipment, ensuring all apparatus are calibrated, clean, and fully operational. Troubleshoot and resolve technical, equipment, or testing complications to ensure minimal disruption to laboratory operations. Adapt to new technologies and maintain professional knowledge necessary for the provision of quality laboratory services.Minimum Position Qualifications: Accredited degree from a Medical Technologist or Medical Laboratory Technician program (required). Certification as an MT/CLS (ASCP) or as an MLT/CLS (ASCP). Ability to work night or day shifts in a 36-hour workweek schedule. Strong commitment to delivering high-quality patient care and achieving superior clinical outcomes. Proven ability to operate complex laboratory equipment and perform precise testing.Preferred Qualifications: Blood Bank experience. Experience in a high-volume lab setting; new graduates must have completed a clinical internship in a comparable environment. Detail-oriented with robust analytical and diagnostic skills. Strong communication skills and the ability to work seamlessly in a team.Skills: Proficient in using laboratory information systems (LIS) and other computer systems pertinent to laboratory technologies. Expertise in maintaining and troubleshooting clinical laboratory equipment. Strong organizational and multitasking skills. Efficient in time management with a proven record of meeting critical deadlines. Capability to handle biological hazards and samples.Benefits: Generous shift differentials for evening, night, and weekend shifts. Sign-on bonus and a full benefits package including health, dental, vision, and retirement plans. Opportunities for ongoing education and professional training. Located in a brand-new facility with the latest in medical technology.

Trusted is seeking an experienced nurse for this exciting travel nursing assignment. Trusted has streamlined the travel nursing experience by enabling nurses to apply directly to jobs without the need for recruiters. This unique approach provides more transparency, eliminates pesky calls from recruiters, and puts more money in your pocket. Join the thousands of nurses across the country who have already made the switch to a more modern way to work.

Experience:

• 12 months of role experience is required with some in the last 12 months.

• 22 months of Medical Surgical Unit experience is required with some in the last 24 months.

• Travel experience is preferred from any number of months.

• Experience with Epic is required from any number of months.

Requirements:

• Candidates must have a Ohio license or compact license (required for submission).

• This role will require floating to multiple units

• Local & travel allowed. Candidates living <60 miles from facility will be processed as local.

• Flu vaccination required after submission. Religious and medical declinations accepted.

Pre-employment modules may be required for this role. Please upload any certifications or health documents you have to your profile to expedite your on-boarding process.

Additional Details:

Education must be from an ACEN or CCNE accredited program.

References must cover at least 1 full year of relevant experience in specialty within the past 3 years.

Oncology experience preferred but not required.

Shift: D/N Rotating or Nights

If you accept a 12D/N rotating contract, you may be scheduled for days, nights, or a combination of both, depending on the department’s needs. Shift assignments are reviewed every 4-week scheduling period, but changes are not guaranteed and are based on staffing priorities at that time.

Weekends - variable based on unit needs

No set/blocked scheduling

*Self-schedule requests - you will enter your schedule requests so we can see your preferred schedule before balancing and posting the final schedule.

Floating required to other MedSurg Oncology units.

*First week of orientation is Mon - Fri dayshift. Second week is 36hrs of on-unit orientation with a preceptor.

Patient Age group: Adult, Geriatrics

Patient Diagnoses: The most common diagnoses include all subtypes of the following – Breast Cancer, Lung Cancer,Prostate Cancer, Pancreatic Cancer, Colon Cancer, Esophageal Cancer, Encounter for antineoplastic chemotherapy

Special Procedures/Unit Details:

-17 James cares for all solid tumor cancers throughout the spectrum of their cancer journey; from new diagnosis, through treatment, and also assisting with transition to end of life care.

-Heavy focus on infection prevention protocols and patient falls

-Cares for patients that have true med surg issues

Skills Required: Telemetry Interpretation, Telemetry monitoring

There is a strict compliance deadline of Tuesday prior to start – no exceptions.

Please note: All candidates must be made aware of the urgency of the Ohio Fingerprinting process. Candidates must complete fingerprints as soon as they sign contract. Travelers who are unresponsive or uncooperative with credentialing are at risk of push/cancel.

RTO required with submission, must be built into contract.

2 professional references are required. At least 1 reference must be from a manager/director or someone in a formal leadership capacity (e.g., a supervisor). Charge RN acceptable for 2nd reference. No coworker references accepted.

Former employees are eligible for a travel assignment once they have been away from the facility for 6 months or more.

Current employees are ineligible to be hired as a traveler at any Ohio State University hospital location.

Details:

• AUTO OFFER - NO INTERVIEW : Please request an interview for one match from this facility at a time. You will not interview with the hiring manager if the facility chooses to extend an offer to you for this position. All time off requests must be submitted at application. Scheduling requests must be worked out with the manager directly upon starting the assignment. Any offers for this job will require a clear “Yes” or “No” response from the nurse within 24hrs or the offer must be declined.

7 days maximum time off

1 reference from last 2 years (Manager/Supervisor reference type) - required for submission

1 reference from last 2 years (Charge/Lead reference type) - required for submission

Proof of identification required

Certifications:

• ONS (Chemotherapy and Biotherapy Provider)

• BLS (Basic Life Support)

• Skills Checklist: Yes
• References: Yes
• License Type: registered
• License State: OH
• Certifications: Chemotherapy and Biotherapy Provider, Basic Life Support

Job Details

• Job Type: Travel
• Nurse/Patient: 1/4-5
• Shift Type: Variable
• Contract Date: 2025-08-25
• Expected Length: 13 weeks
• Hours per Shift: 12
• Shifts per Week: 3