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Cigna Rn Remote Jobs in San Ramon, CA (NOW HIRING)

... (RN, EMT, Paramedic, PA, MD, DO, etc.) * Professional experience in military/government (Active Duty, Former Duty, etc) * Experience working with a sales team in a remote work environment.

... (RN, EMT, Paramedic, PA, MD, DO, etc.) * Professional experience in military/government (Active Duty, Former Duty, etc) * Experience working with a sales team in a remote work environment.

... RN or pharmaceutical experience preferred but not required. * Minimum of 4 years of clinical trial management and 2+ years clinical research associate with on-site/remote clinical monitoring ...

Clinical Trial Manager

San Francisco, CA · On-site +1

$140K - $170K/yr

... an RN (2- or 3-year certificate) * Relevant clinical trial experience in the pharmaceutical or ... This position is for remote work and may require domestic or international travel up to 25% (as ...

Recruiter

San Mateo, CA · Remote

$70K - $80K/yr

... RNs, LCMs, etc) * Demonstrate a willingness to actively recruit for a wide range of roles across ... Previous remote experience * Start-up experience Additional Information * The hiring process for ...

Will not consider fully remote candidates. Job Responsibilities: * Provides ongoing financial ... BA / BS / RN with 8 or more years' relevant clinical or related experience in life sciences or MA ...

Will not consider fully remote candidates. Job Responsibilities: * Provides ongoing financial ... BA / BS / RN with 8 or more years' relevant clinical or related experience in life sciences or MA ...

Showing results 41-55

Cigna Rn Remote information

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How much do cigna rn remote jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for cigna rn remote in San Ramon, CA is $50.19, according to ZipRecruiter salary data. Most workers in this role earn between $38.41 and $59.62 per hour, depending on experience, location, and employer.

What is a Cigna RN Remote?

A Cigna RN Remote job is a work-from-home nursing position where registered nurses provide telephonic or virtual patient care, case management, or health coaching. Nurses in this role typically assess patient needs, coordinate care plans, and educate members on managing their health conditions. These positions may be in areas like utilization management, disease management, or triage nursing. The job requires an active RN license, clinical experience, and strong communication skills.

What skills and qualifications are needed for a Cigna RN Remote?

To thrive as a Cigna RN Remote, you need an active RN license, strong clinical assessment abilities, and experience in case management or telehealth nursing. Familiarity with electronic health record (EHR) systems, secure communication platforms, and care coordination software is typically required. Excellent time management, self-motivation, and effective virtual communication are key soft skills for this remote position. These competencies are vital for delivering high-quality patient care, maintaining compliance, and efficiently collaborating within a virtual healthcare team.

What challenges do Cigna RN Remote professionals face, and how can they be managed?

Cigna RN Remote professionals often face challenges such as balancing multiple case loads, adapting to limited in-person patient interactions, and maintaining clear communication with both patients and colleagues in a virtual setting. To manage these challenges, it's important to develop strong organizational skills, leverage digital health tools effectively, and proactively participate in virtual team meetings. Continuous learning and regular collaboration with support staff also help remote RNs stay informed and connected. By staying engaged and utilizing available resources, remote nurses can overcome common hurdles and excel in providing patient-centered care from home.

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Infographic showing various Cigna Rn Remote job openings in San Ramon, CA as of September 2026, with employment types broken down into 83% Full Time, and 17% Part Time. Highlights an 100% Remote job distribution, with an average salary of $104,398 per year, or $50.2 per hour.

Senior Manager/Associate Director Clinical Monitoring Strategy & Optimization

Menlo Park, CA • On-site, Remote

Full-time

Re-posted 7 days ago


Job description

About Us:
Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com
As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture.
Job Title: Sr. Manager/Associate Director, Clinical Monitoring Strategy and Optimization
Location: Remote OR Hybrid 3 days/week if located near office in either Waltham, MA or Menlo Park, CA will be required.
Role Overview:
We are seeking an experienced and highly motivated Sr. Manager/Associate Director of Clinical Monitoring Strategy and Optimization to provide strategic and operational leadership for clinical monitoring activities across our development programs. This individual will play a critical role in building and scaling clinical operations infrastructure within a fast-paced emerging biotech environment.
The successful candidate will oversee CRO monitoring performance, ensure high-quality execution of clinical trials, and contribute to the development of monitoring processes, vendor oversight strategies, and inspection readiness activities. This role requires a hands-on leader who is comfortable operating both strategically and tactically in a lean organization.
Key Responsibilities:
Clinical Monitoring Leadership
  • Lead and oversee clinical monitoring activities for Phase 1-3 clinical trials conducted globally and/or domestically.
  • Serve as the internal expert for monitoring strategy, site management, and risk-based monitoring approaches.
  • Provide oversight and management of CROs, CRAs, and other external vendors to ensure quality, timelines, and budget adherence.
  • Review monitoring plans, trip reports, metrics, and monitoring deliverables for quality and compliance.
  • Partner cross-functionally with Clinical Development, Clinical Science, Data Management, Biostatistics, Medical Writing, Pharmacovigilance, Regulatory Affairs, and Quality Assurance.

Vendor and CRO Oversight
  • Establish effective CRO oversight and governance processes.
  • Monitor CRO performance through KPIs, metrics, and regular operational reviews.
  • Escalate and resolve study conduct issues proactively.
  • Participate in vendor selection, qualification, and contract review activities.

Trial Execution and Compliance
  • Ensure studies are conducted in compliance with ICH-GCP, SOPs, protocol requirements, and applicable regulations.
  • Support development and review of key study documents including Monitoring Plans, Risk Management Plans, Study Oversight Plans, Clinical Trial Management Plans, and Site Management Plans.
  • Contribute to inspection readiness activities and support regulatory inspections and audits.

Operational Process Development
  • Help build scalable clinical monitoring infrastructure appropriate for a growing biotech company.
  • Develop and refine SOPs, work instructions, templates, and monitoring processes.
  • Drive continuous improvement initiatives focused on quality, efficiency, and operational excellence.
  • Implement and optimize risk-based monitoring methodologies and centralized monitoring approaches where appropriate.

Team Leadership and Mentorship
  • May directly manage CRAs and/or Clinical Trial Managers as the organization grows.
  • Mentor junior clinical operations staff and contribute to team development.
  • Foster a collaborative, accountable, and quality-focused culture.

Qualifications:
Required
  • Bachelor's degree in life sciences, nursing, or related discipline.
  • 6-8+ years of clinical operations experience within biotech, pharmaceutical, or CRO environments.
  • Significant experience overseeing clinical monitoring activities in interventional clinical trials.
  • Strong knowledge of ICH-GCP, FDA, EMA, and global regulatory requirements.
  • Experience managing CROs and external vendors.
  • Demonstrated ability to work effectively in a small, fast-moving biotech environment.
  • Excellent communication, organizational, and problem-solving skills.
  • Extensive domestic and international travel as needed (approximately 60-80%).

Preferred
  • Bachelor's degree or equivalent required.
  • Advanced degree (MS, MPH, PharmD, PhD, or RN) preferred.
  • Experience in rare disease, immunology, oncology, or other relevant therapeutic areas.
  • Experience supporting NDA/BLA-enabling studies and regulatory inspections.
  • Experience implementing risk-based monitoring strategies and oversight models.
  • Prior people management experience.

Desired Leadership Competencies
  • Strategic thinker with strong execution skills
  • Comfortable with ambiguity and rapid change
  • Hands-on and solutions-oriented
  • Strong collaborator and relationship builder
  • High attention to detail and commitment to quality
  • Ability to influence cross-functional teams and external partners

Compensation:
  • An appropriate financial package will be developed for the successful candidate to include a competitive base salary and equity, with a performance-related bonus opportunity.
  • The anticipated salary range for Sr. Manager is $161,000 - $187,000 and for Associate Director level is $182,000 - $208,000. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Oruka is a multi-state employer, and this salary range may not reflect positions that work in other states.

Location: Remote OR Hybrid 3 days/week if located near office in either Waltham, MA or Menlo Park, CA will be required.
We're looking forward to hearing how you can contribute to our team and mission. Join us in shaping the future of our company and making a real impact every day
Salary Range for the Role
$161,000-$208,000 USD
What We Offer:
  • A chance to be part of a vibrant startup culture where your work can directly impact bringing new medicines to patients.
  • Competitive salary and benefits package.
  • A supportive and inclusive team environment where everyone is encouraged to bring their authentic selves to work.
  • Opportunities for professional growth and development.