Role Description The Registered Nurse, Clinical Delivery (RN) in this role will manage the communication of critical and abnormal lab results to patients, ensuring compliance with state licensure requirements. This includes: - Contacting patients and documenting communications - Following up on lab escalations - Collaborating with providers to ensure all patient interactions are appropriately managed and documented - Providing patient education on lab results and necessary next steps in care - Serving as a point of escalation for the Member Services team - Liaising with the Clinical Conduct Team to resolve issues related to lab results - Assisting in training and educating the Member Services team This role is critical in ensuring timely patient communication and maintaining compliance with clinical and legal standards. This is a part-time position. Qualifications - Strong analytical capabilities - Exceptional communication skills - Commitment to fostering a patient-centered environment - Strong attention to detail - Ability to manage multiple patients efficiently - Ability to work independently while collaborating with a larger clinical team Requirements - Active RN licensure with a commitment to compliance and regulatory standards - Compact Licensure required; additional licenses may be required - BSN or equivalent degree preferred - Minimum of 3 years of experience as a working nurse, clinical research, medical communications, and/or related field - Proficiency in Salesforce or other EMR systems for documenting patient interactions - Willingness to maintain and obtain additional state licenses as needed Benefits - Remote work within the United States - Structured on-call system for coverage - Less than 10% travel requirements - Expected pay range: $34.00 - $48.00 USD per hour for full-time team members Company Description Care Access is working to make the future of health better for all. We bring world-class research and health services directly to communities that often face barriers to care. We are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need, and contribute to the medical breakthroughs of tomorrow. - Programs like Future of Medicine and Difference Makers - Partnerships, technology, and perseverance to reimagine clinical research and health services

Role Description Are you a licensed mental health professional looking for flexible, remote work opportunities? Join ifeel and help us provide accessible, convenient, and confidential care through our innovative online platform. Depending on your role, responsibilities may include: - Chat Therapy: Provide text-based support to clients, offering guidance and evidence-based care in real time. - Video Therapy: Conduct face-to-face virtual sessions with clients. Qualifications - Active licensure as a mental health professional in India. - Registration as a Freelancer. - Fluency in English and Hindi; proficiency in additional languages is a plus. - Reliable high-speed internet connection and familiarity with virtual communication tools. - Strong communication and interpersonal skills. - Commitment to ethical and confidential care. Requirements - Experience with telehealth or online therapy platforms. - Multilingual abilities are a strong plus. - Specialized training or certifications (e.g., CBT, DBT, trauma-informed care). Benefits - Flexibility: Work when and where it suits you. - Variety of Roles: Choose between chat therapy, video therapy, or triage support based on your strengths and preferences. - Continuous Learning and Support: Access regular training and support to enhance your abilities and grow in your profession. - Global Community: Engage with a diverse community of professionals worldwide, fostering collaboration and mutual support. - Focus on Care: Focus solely on your clients' needs without the burden or the cost of marketing fees and websites. We send clients your way at no extra expense. - Remote Work: Provide therapy from the comfort of your home or office. - Competitive Pay: Earn consistent income with opportunities for bonuses.

Job Title: Clinical Research Coordinator Location Philadelphia, Pennsylvania, USA category Clinical 28 USD - 31.25 USD/hour Job Description This role supports cutting-edge oncology clinical trials by coordinating all aspects of in-hospital clinical research, with a focus on patient recruitment, informed consent, regulatory compliance, and accurate documentation. The Clinical Research Coordinator works closely with investigators and study teams to ensure that studies follow Good Clinical Practice (GCP) guidelines and human research protection regulations while contributing to high-profile, pharma-backed oncology research. Responsibilities - Recruit, pre-screen, and enroll patients into oncology clinical trials in accordance with study protocols and eligibility criteria. - Explain the informed consent process clearly and thoroughly to potential participants, ensuring they understand study procedures, risks, and benefits before consenting. - Obtain and document informed consent from patients, maintaining complete and accurate consent records. - Conduct detailed chart reviews and pre-screening of patients to identify appropriate candidates for clinical trials. - Collect and manage study documents, including protocols, regulatory documents, informed consent forms, case report forms, and source documents. - Document adverse events accurately and promptly, and support adverse event reporting in compliance with regulatory requirements and institutional policies. - Prepare and submit Institutional Review Board (IRB) applications and related regulatory documentation, ensuring adherence to IRB and human research protection regulations. - Coordinate day-to-day clinical trial activities in an in-hospital setting, ensuring adherence to Good Clinical Practice (GCP) and study timelines. - Communicate effectively with investigators, sponsors, and multidisciplinary clinical teams to support smooth study operations and patient care. - Maintain organized study files and records to support monitoring, audits, and regulatory reviews. - Support both industry-sponsored and investigator-initiated studies in a high-volume oncology research environment. Essential Skills - Minimum of 2+ years of clinical research experience, preferably in an in-hospital setting. - Demonstrated experience with patient recruitment, pre-screening, and consenting for clinical trials. - Hands-on experience documenting adverse events and supporting adverse event reporting processes. - Working knowledge of Institutional Review Board (IRB) processes and human research protection regulations. - Strong understanding of Good Clinical Practice (GCP) and clinical trial conduct. - Experience as a clinical research coordinator or in a closely related clinical research role. - Proven ability to work with oncology patients and support oncology clinical trials. - Effective verbal and written communication skills for interacting with patients, clinicians, and research teams. - Strong organizational skills with the ability to manage multiple studies and a high-volume workload. - Proficiency in performing chart reviews and maintaining accurate, complete study documentation. Additional Skills & Qualifications - BA/BS degree preferred. - Prior experience with in-hospital clinical research environments. - Experience working on pharma-backed or sponsor-driven clinical trials. - Background or exposure to oncology research and patient populations. - Ability to explain complex medical and research concepts in a clear and compassionate manner. - Comfort working within large academic or research institutions with multiple stakeholders. Work Environment The position is based in a combination of office and hospital/outpatient surgery settings within a large academic research campus. The workload is fast paced and high volume, supporting both industry-sponsored and investigator-initiated oncology studies. The role typically requires five days on site initially, with the opportunity to transition to a hybrid schedule after approximately three to four months, working three days on site and two days remotely each week. The environment features state-of-the-art equipment and access to high-profile, sponsor-backed oncology studies, offering the opportunity to contribute to leading-edge cancer research in a prestigious academic research institute. Job Type & Location This is a Contract to Hire position based out of Philadelphia, PA. Pay and Benefits The pay range for this position is $28.00 - $31.25/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a hybrid position in Philadelphia,PA. Application Deadline This position is anticipated to close on Jul 3, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Clinical Research Financial Analyst (Remote) Location: United States Job Description: Overview The Office of Cancer Research is seeking a highly skilled Clinical Research Financial Analyst to support a robust portfolio of adult and pediatric oncology clinical trials. Key Responsibilities - Manage financial operations of assigned clinical research studies, including planning, tracking, and reconciliation of study finances - Perform clinical trial invoicing, reconciliation, and accounts receivable activities - Build and maintain study calendars in OnCore (CTMS) - Utilize Workday (ERP) and EPIC (EMR) for financial and clinical data management - Conduct and review coverage analyses, study budgets, and clinical trial agreements (CTAs) - Support budget development and negotiation with sponsors - Coordinate patient charge segregation and ensure billing compliance - Lead or support study start-up and closeout financial activities - Serve as a key liaison between faculty, research teams, finance, and institutional departments - Provide mentorship and guidance to junior and mid-level staff - Collaborate with investigators and leadership on financial planning for sponsored research Required Qualifications - Bachelor's degree in Finance, Business Administration, or related field (or 10+ years of relevant research administration experience) - 3-5+ years of experience in a clinical research or academic medical center environment - Hands-on experience with: - OnCore (required) - Workday (required) - EPIC (preferred) - Strong experience in clinical trial invoicing and reconciliation - Knowledge of coverage analysis, budgets, and clinical trial agreements - Familiarity with federal and non-federal funding regulations - Excellent communication and interpersonal skills, with ability to work cross-functionally - Oncology clinical research experience - Experience supporting adult and pediatric hematology/oncology studies - Knowledge of grant applications and research funding management - High proficiency in Microsoft Excel and financial reporting tools Job Type & Location This is a Contract to Hire position based out of Providence, RI. Pay and Benefits The pay range for this position is $36.00 - $40.86/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully remote position. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.