Role Description We are seeking a dedicated medical oncologist contractor to join our Virtual Cancer Clinic care team. In this contractor role, you will have the opportunity to provide high-quality care to patients with cancer. Your responsibilities include: - Pre-treatment workup - Treatment planning - Collaboration and support for local treatment management - Ongoing cancer maintenance and risk-reduction therapy - Symptom assessment and management - Cancer surveillance and survivorship care All services will be delivered remotely through a telehealth platform using video, audio, and asynchronous messaging. The ideal candidate will be passionate about reducing the impact of cancer on populations, skilled in utilizing telehealth technology, and committed to delivering best-in-class cancer care. How You'll Contribute - Conduct clinical assessments and diagnostic evaluations - Develop treatment and management plans - Deliver direct care, including ordering laboratory, imaging, procedures, referrals, and prescriptions - Closely collaborate with local clinicians to deliver evidence-based cancer care - In collaboration with Color’s primary care team, assess patients with cancer screening abnormalities and facilitate diagnosis of cancer - Determine guideline-based oncology and symptom treatment plans - Identify optimal treatment locations and order referrals to appropriate local care teams for evaluation and treatment - Educate patients about guideline-based cancer treatment options, including clinical trials and potential risks and benefits - Prepare patients for local visits and assist patients with clinical decision-making - Assess and manage oncology and treatment-related symptoms and complications as appropriate for a virtual setting - Develop clinical protocols and best practices for care delivery - Provide compassionate, empathetic care, establishing close, trust-based relationships with patients - Participate in care team sessions to monitor patient progress, provide updates, and collaborate on targeted support plans - Maintain thorough and detailed documentation of encounters with patients Qualifications - MD or DO, fellowship-trained and board-certified in Medical Oncology - Valid state medical license in good standing, with willingness to obtain licensure in all 50 states - Minimum of 2 years independent oncology-related clinical practice experience post-fellowship - Broad expertise across a range of cancers - Friendly, compassionate manner with a passion for helping patients thrive - Deep understanding of, and motivation to address, the care gaps faced by cancer patients and their caregivers at every stage of treatment - Strong clinical skills with a commitment to evidence-based, patient-centered, high-quality care - Effective collaborator with a team-oriented mindset - Exceptional written and verbal communication skills, emphasizing empathy and active listening - High ethical standards and professionalism - Excellent organizational skills with the ability to multitask and excel in fast-paced environments - Proficient telehealth skills, including patient care via video and audio, asynchronous messaging, and use of electronic health records and digital telehealth tools - Preferred: Licensure in a state participating in the IMLC - Preferred: Experience collaborating with cross-functional technical and operations teams Hourly Rate Starting at $300 per hour. The actual hourly rate is dependent upon many factors, such as work experience, market data, skills, geographic location, and business need. The hourly rate is subject to change and may be modified in the future. Equal Opportunity Employer Color is an equal opportunity employer. In accordance with anti-discrimination law, it is the purpose of this policy to effectuate these principles and mandates. Color prohibits discrimination and harassment of any type and affords equal employment opportunities to employees and applicants without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. Color conforms to the spirit as well as to the letter of all applicable laws and regulations.

Role Description Premier Research is looking for a Senior Clinical Research Associate, Sponsor-dedicated (Contract) to join our Functional Services Provider (FSP) team. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success. We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires. Your ideas influence the way we work, and your voice matters here. As an essential part of our team, you help us deliver the medical innovation that patients are desperate for. Join us and build your future here. What You’ll Be Doing: - Conducts source verification by comparing data recorded on Case Report Forms against source documents, verifying Informed Consent Forms for accuracy and completeness, and reviewing regulatory documents and device accountability records. - Issues, investigates, and resolves any data discrepancies identified during source verification activities. - Maintains thorough documentation and proper escalation of issues related to visit reports. - Ensures any identified non-compliance issues are addressed. - Ensures that all reportable events are identified, clearly documented and reported per protocol and as per applicable requirements and regulations. - Manages study contracts, requests/collects relevant investigator/site documentation (i.e. regulatory documents, financial disclosure forms, curriculum vitae/medical license), and reviews and approves documents in applicable database. - Performs budget negotiations with clinical trial sites. Qualifications - Experience in Neurology or Psychiatry, including work with Schedule I controlled substances, is required. - Bachelor's degree, or international equivalent from an accredited institution, preferably in a clinical, biological, scientific, or health-related field or equivalent combination of education, training and experience. - 5 to 7 years of practical experience conducting continuous independent onsite monitoring of clinical research sites as well as site management activities. Alternately, must have proven experience in all primary job functions. - Strong analytical and organization skills, able to work independently and manage multiple projects simultaneously in a fast-paced environment with changing priorities. - Knowledge of International Conference on Harmonization (ICH)/Good Clinical Practices (GCP) and/or ISO14155 requirements as well as detailed knowledge of the relevant country specific regulatory requirements for conducting clinical trials. - Willingness to travel up to 70-85%. Requirements - This is a 1099 12-month contract position with the potential to extend and renew after 1 year. Company Description Premier Research is proud to be an equal opportunity employer that is compliant with all federal guidelines. All qualified applicants will receive equitable consideration without regard to race, color, religion, sexual orientation, gender identity, national origin, disability or veteran status.

Role Description Premier Research is looking for a In-House Clinical Research Associate I, Sponsor-Dedicated (Contract) to join our Functional Services Provider (FSP) team. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success. We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires. Your ideas influence the way we work, and your voice matters here. As an essential part of our team, you help us deliver the medical innovation that patients are desperate for. Join us and build your future here. - Partners with cross-functional team members and study sites throughout all phases to offer support of numerous trial elements for the clinical operation teams. - Carry out remote monitoring of clinical trials. - Serves as the secondary contact for sites supporting CRAs. - Responsible for the proper reporting and follow up of SAEs and ensures all reportable events are identified, clearly documented and reported per protocol as well as applicable requirements and regulations. - Ensures any identified non-compliance issues are addressed, clearly communicated, documented and escalated as required through monitoring visits, analyzing study metrics, and general study data overview. - Assists with audit/inspection readiness, study start-up activities, data listing reviews, monitoring visit support and issue resolution. Qualifications - Experience in Neurology or Psychiatry, including work with Schedule I controlled substances, is highly preferred. - Bachelor's degree, or international equivalent from an accredited institution, preferably in a clinical, biological, scientific, or health-related field or equivalent combination of education, training and experience. - 3 to 5 years of practical experience in clinical trials. Alternately, a proven experience in all primary job functions. - Participate in study-specific meetings, teleconferences and training as needed. - Demonstrates excellent English verbal and written communication skills. - Proven ability to drive a successful customer experience through positive customer interactions, provision of quality and timely deliverable, and task ownership. - Preferred Location: East Coast / Central. Requirements - This is a 1099 12-month contract position with the potential to extend and renew after 1 year. Company Description Premier Research is proud to be an equal opportunity employer that is compliant with all federal guidelines. All qualified applicants will receive equitable consideration without regard to race, color, religion, sexual orientation, gender identity, national origin, disability or veteran status.

Role Description As a(n) Anly Clinical Developer, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by: - Serve as a requirements analyst for the grouping, editing and reimbursement component team. - Deliver on quarterly release goals for assigned components. - Gather and interpret requirements as published by federal and state agencies. - Document requirement specifications in DOORS. - Review requirements with product engineers and quality analysts prior to release. - Work closely with component engineers in implementing software modifications. - Support internal teams with escalated customer issues. Qualifications - Bachelor or higher (completed and verified prior to start) from an accredited institution in Health Information Management, Business Administration, Hospital Administration or related applicable technical/health care field. - Four (4) years of experience. - 3+ years of healthcare related computer science experience working with patient classification systems and/or data analysis. - Excellent reading comprehension including the ability to translate and communicate complex regulatory documents both verbally and in written format to diversified audiences with various skill levels. - An understanding of medical grouping, editing, and coding, within the healthcare industry. - Knowledge of and experience with ICD-9, ICD-10, HCPCS/CPT coding practices as well as familiarity with various groupers (MS-DRG, APC, APR, etc.). - Ability to multitask, with minimal direction, while meeting aggressive project deadlines. - Experience with HIS Products. - Proven data analysis skills. - Strong technical background. - Proven ability in working/coordinating with 3rd party entities. - Experience with billing. - Claims adjudication. - Patient accounting/patient financial services. - Working knowledge of Medicare, Medicaid and commercial payment methodologies and commercial insurance contracts. Requirements - Work location: Remote - Travel: May include up to 5% domestic - Relocation Assistance: Not authorized - Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status). Benefits - Competitive pay and benefits. - Medical, Dental & Vision. - Health Savings Accounts. - Health Care & Dependent Care Flexible Spending Accounts. - Disability Benefits. - Life Insurance. - Voluntary Benefits. - Paid Absences and Retirement Benefits.