Documentation Jobs in Maine
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Search Results - Documentation Jobs in Maine
Adecco-Auburn (ME)
Adecco is partnering with a successful manufacturing organization in Auburn, ME to hire a Safety Documentation Specialist who thrives in a hands-on, fast-paced environment. This is a unique hybrid role combining shop-floor safety leadership...
adecco.com -
DayOne-Windham (ME)
of license renewals.
This will be structured as a FFS position but will have an admin rate that will cover fixed documentation time and training hours.
*Duties:*
• Facilitate individual, group, and family therapy
• Implement behavioral therapy...
MRG Exams-Orono (ME)
for U.S. Veterans as part of the VA's disability benefits process. This role involves conducting focused, in-person physical exams and reviewing medical records electronically to complete the required documentation for the VA.
Key Responsibilities...
1 similar job: Brewer
MaineGeneral Health-Augusta (ME)
Job Summary: Provides clinical leadership and strategic support in utilization management (UM) and clinical documentation improvement (CDI), ensuring regulatory compliance, optimizing resource use, and enhancing patient outcomes. Job Description...
Carenest Health Services-Portland (ME)
safety, and quality improvement initiatives.
Manage staffing levels, assignments, and coverage based on patient acuity and census.
Conduct rounds and audits to ensure proper documentation and adherence to care standards.
Address and resolve patient...
American Traveler-Damariscotta
hours per day, 5 days per week
• Caseload of approximately 10 patients per day
• 45-minute evaluation and treatment sessions with 30 minutes of built-in documentation time per day
• 13-week contract duration
Requirements
• Minimum 2 years of physical...
American Traveler-Damariscotta
8:00 AM–4:30 PM, 8 hours per day, 5 days per week
• Caseload of approximately 10 patients per day
• 45-minute evaluation and treatment sessions with 30 minutes of built-in documentation time per day
• 13-week contract duration
Requirements...
Hayman Daugherty Associates-Monroe (ME)
Utilize the provider portal for efficient completion of evaluations and documentation. Record Review: Active participation in record reviews required to maintain thorough patient assessments and documentation. Administrative Work: Regular follow-up...
Brett DiNovi & Associates-Skowhegan
and oversee individualized treatment plans
• Provide supervision to RBTs and direct parent training
• Maintain strong clinical documentation and data-driven decision-making
*This Role Is Great For You If You:*
✔ Enjoy working directly with students
✔ Want...
LocumJobsOnline-Bangor
utilizes the Meditech electronic medical record system for patient documentation and care coordination.
About the Facility Location
Maine offers diverse coastal and mountain landscapes with regional attractions including outdoor recreation and year-round...
Takeda Pharmaceutical-Cambridge
for ensuring global submissions and lifecycle compliance for devices and combination products (e.g., IDE, 510(k), De Novo, PMA, CE marking under MDR, technical documentation, variations/changes, vigilance). Partners with regional leads, quality, and vendors...
LocumJobsOnline-Lewiston
utilizes the Meditech electronic medical record system for patient documentation and care coordination.
About the Facility Location
Maine offers diverse coastal and mountain landscapes with regional attractions including outdoor recreation and year-round...
Takeda Pharmaceutical-Cambridge
for ensuring global submissions and lifecycle compliance for devices and combination products (e.g., IDE, 510(k), De Novo, PMA, CE marking under MDR, technical documentation, variations/changes, vigilance). Partners with regional leads, quality, and vendors...
Fusion Medical Staffing-Saco (ME)
as an RN
• Proficient in OASIS documentation
• Valid RN license in compliance with state regulations
• BLS certification (AHA/ARC)
Preferred Qualifications:
• Home Health Nursing Certification (RN-BC)
• Other certifications and licenses may be required...
Takeda Pharmaceutical-Cambridge
for ensuring global submissions and lifecycle compliance for devices and combination products (e.g., IDE, 510(k), De Novo, PMA, CE marking under MDR, technical documentation, variations/changes, vigilance). Partners with regional leads, quality, and vendors...
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