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Senior R1 Rcm Medical Coding Jobs in New Jersey (NOW HIRING)

SOFIE

Sr. Radiochemist

Totowa, NJ · On-site

$90K - $100K/yr

Sr Radiochemist, RCM Project Lead Reports To: Director, Radiopharmaceutical Contract Manufacturing (RCM) Compensation $90k - $100k Overview The Senior Radiochemist will lead the development ...

Addison Group

Medical Biller

Pennsauken, NJ · On-site

$20 - $25/hr

Our client is a well-established RCM company working with local health systems to handle billing ... Process insurance claims, ensure accurate coding, and manage billing disputes. * Work with various ...

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Senior R1 Rcm Medical Coding information

Can I make 6 figures as a medical coder?

Senior R1 Rcm Medical Coders with extensive experience, certifications, and specialization in complex coding can potentially earn six-figure salaries, especially in high-demand healthcare settings. However, most medical coding roles typically offer salaries below six figures, and reaching that level often requires additional skills, certifications, or managerial responsibilities.

Is R1 Careers legit?

R1 RCM is a healthcare technology and revenue cycle management company, not a job title. If referring to employment opportunities with R1 RCM, it is a legitimate organization that offers roles such as Senior R1 RCM Medical Coder, which typically require relevant certifications and experience. Job seekers should verify openings directly through official company channels.

What is the difference between Senior R1 Rcm Medical Coding vs Medical Coding Specialist?

AspectSenior R1 Rcm Medical CodingMedical Coding Specialist
CertificationsAHIMA/ACMEC certifications, CPC, CCSSimilar certifications, often CPC or CCS
Work EnvironmentHealthcare facilities, RCM companies, remote optionsHospitals, clinics, remote or onsite
Job ResponsibilitiesComplex coding, audits, mentoringStandard coding, claim submission
Experience LevelAdvanced, with years of experienceEntry to mid-level

Senior R1 Rcm Medical Coders typically handle complex cases, audits, and mentoring, requiring more experience and advanced certifications. Medical Coding Specialists focus on standard coding tasks and claim submissions, often at entry or mid-level. Both roles share similar certifications and work environments but differ in complexity and responsibility.

What is the highest paid medical coder job?

Senior R1 Rcm Medical Coding roles are among the highest paid in medical coding, often due to advanced expertise, certifications, and experience. These positions typically offer higher salaries compared to entry-level coding jobs and may involve specialized knowledge of complex medical procedures and billing systems.

Is medical coding worth it in 2026?

Senior R1 Rcm Medical Coding is a stable career with consistent demand due to ongoing healthcare documentation needs. Certified coders with strong knowledge of coding systems like ICD-10 and CPT are likely to find good job prospects, especially as healthcare regulations evolve. The profession offers opportunities for remote work and flexible schedules, making it a viable career choice in 2026.
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Senior R1 Rcm Medical Coding jobs near you

Sr. Radiochemist

SOFIE

Totowa, NJ • On-site

$90K - $100K/yr

Other

Posted 7 days ago

SOFIE rating

8.7

Company rating: 8.7 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

13th of 73 rated pharmaceutical

Job description

Sr Radiochemist, RCM Project Lead Reports To: Director, Radiopharmaceutical Contract Manufacturing (RCM) Compensation $90k - $100k Overview The Senior Radiochemist will lead the development, implementation, and validation of manufacturing and analytical methods of new diagnostic and therapeutic radiopharmaceuticals for SOFIE within the Radiopharmaceutical Contract Manufacturing Division. Working closely with SOFIE’s pharmaceutical partners, they will ensure that these radiopharmaceuticals are in full compliance with all regulatory requirements (specifically, 21 CFR 211 and 212). Essential Duties and Responsibilities Lead the development of protocols for the production and analysis of clinical/commercial-grade radiopharmaceuticals, validate these methodologies against quality requirements, and implement them for regular production of radiopharmaceuticals for preclinical or clinical use according to cGMP standards.

It is expected that the development of these protocols will involve both the application of scientific principles and rationales and also adherence to regulatory requirements. Write clear Standard Operating Protocols (SOPs) for these protocols. Review existing SOPs and suggest logical modifications based on either scientific rationales and/or regulatory requirements.

Serve as lead technical support and/or training for production staff at SOFIE sites, either remotely or on-site. Write corporate exception reports and other regulatory documents, such as risk assessments, change controls, etc. Conduct production or quality control analytical tests for regular production of radiopharmaceuticals for preclinical or clinical use according to cGMP standards.

Install, qualify, and maintain laboratory equipment on site. Validate existing production or analytical methods on existing or new equipment. Lead the collaboration with other production radiochemists and quality control chemists as required to ensure successful protocol development and radiopharmaceutical production.

Maintain all qualification and validation requirements for entering ISO classified areas. Maintain a clean and safe working environment and perform radiation safety duties in compliance with safety and pharmaceutical regulations. Maintain accurate radiopharmaceutical production records and test/validation results.

Write reports, presentations, and other documentation summarizing experimental/production data. Coordinate with the Radiopharmaceutical Contract Manufacturing team’s activities to reach defined objectives. Liaise with our contract partners (e.g.

biotech and pharma). Other duties as assigned. Qualifications Degree in chemistry, engineering or natural sciences preferred but will entertain applicants with relevant education and work experience.

PhD preferred. 5 years’ experience preferred in radiopharmaceutical manufacturing and QC in a GMP or academic environment Expertise in laboratory procedures and analytical chemistry techniques required (thin layer chromatography, GC, HPLC, preparative HPLC, Radiometric Detectors, endotoxin, etc.). Experience with the use of automated synthesis modules and maintenance of automated modules required.

Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals required. Knowledge of cGMP requirements, aseptic process (cleanroom environment), and equipment qualification preferred. Efficient in the use of MS Office Suite required.

Ability to be detail-oriented, accountable, patient, organized, and work in a team environment with minimum supervision required. Strong technical writing skills required. Excellent organizational skills required.

Ability to work various shifts and weekends required. Travel: up to 15 % domestically.

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