Writing.io Jobs

Company Overview:Blink Health is the fastest growing healthcare technology company that builds products to make prescriptions accessible and affordable to everybody.

Please submit your CV in English and indicate your level of English proficiency.

Mindrift connects specialists with project-based AI opportunities for leading tech companies, focused on testing, evaluating, and improving AI systems. Participation is project-based.

What this opportunity involves

We’re looking for US-based, actively practicing physicians (MD/DO) to evaluate clinical EHR vignettes for a medical AI evaluation program. General and internal medicine are our main focus. While each project involves unique tasks, contributors may:

• Evaluate clinical EHR vignettes paired with a question, a proposed answer, and a distractor “trap” answer across diagnosis and treatment tasks, spanning cardiovascular, nervous, hematologic, respiratory, digestive, urinary, reproductive, musculoskeletal, and integumentary systems;
• Score the clinical reasoning quality of benchmark items: vignette accuracy and completeness, whether the vignette gives the answer away, answer correctness and gradeability, and trap quality;
• Check whether the reasoning chain reaches the answer from vignette facts alone, correct reasoning traces, and write short rationales;
• Work within three independent blind reads, followed by physician adjudication. Real clinical complexity only. You’re improving the AI tools you’ll eventually use yourself.

If you’re a practicing physician ready to take on this challenging and engaging project, join us!

What we look for

This opportunity is a good fit for US-based physicians open to part-time, non-permanent projects. Ideally, contributors will have:

• Medical degree (MD or DO) and an active, unrestricted US medical license (verified with the issuing medical board);
• Board certification or completed residency training, with recent direct patient care (attending-level preferred);
• Broad, multi-system diagnostic and treatment experience (internal, family, emergency, or hospital medicine);
• Strong clinical reasoning: differential diagnosis, next-step management, and application of evidence-based guidelines;
• Prior experience in medical AI evaluation, clinical content or exam-question review, or medical annotation/QA (a plus);
• Strong written English (C1+).

This opportunity is not fit to medical students, unlicensed medical graduates, non-physician clinicians (NPs, PAs, nurses, pharmacists), or non-clinical healthcare titles.

Project time expectations

For this project, tasks are estimated to require around 10-20 hours per week during active phases, based on project requirements. This is an estimate, not a guaranteed workload, and applies only while the project is active. Tasks must be submitted by the deadline and meet the listed acceptance criteria to be accepted.

Compensation

Paid per accepted task. Your rate depends on the qualification tier you reach and how efficiently you complete tasks — up to the equivalent of $70/hr. Because payment is per approved task, a faster pace raises your effective hourly rate.

POSITION SUMMARY The Associate Area Medical Director (Associate AMD) is a physician contributor operating within a defined regional geography under the guidance of an Area Medical Director or Medical Affairs...

JOB SUMMARY: The Sr. Clinical Data Manager is responsible for developing and managing all aspects of the global clinical study data management process from start-up to database lock and regulatory submission support.

Discover Vanderbilt Health: With eight hospitals and over 180 clinics, we are the region’s largest comprehensive academic health system.

Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed,...

Due to our continued growth, Precision for Medicine is looking for a Senior Feasibility Associate/Feasibility Manager to join our European team. This position can be covered fully remotely in UK,...

Job Description: Sharecare is a digital healthcare company that delivers software and tech-enabled services to stakeholders across the healthcare ecosystem to help improve care quality, drive better outcomes, and lower costs.

An opportunity to help patients who have run out of options For many people living with chronic pain, the journey has been long. They have tried multiple medications, procedures and...

, remoteLehrer Family Chiropractic is seeking a highly skilled and motivated Remote Telehealth Physician to join our team in Melville, New York.

Amaze Health delivers concierge-style virtual care that feels like having a trusted “doctor friend” on call 24⁄7, for everything from sudden illnesses to chronic conditions and mental health. As a true partner, we simplify the healthcare maze, guiding patients with clarity, compassion, and confidence while empowering them to take control of their health. Beyond treatment, we provide partnership, helping people feel heard, supported, and cared for throughout their journey. Join us as we transform healthcare, one patient at a time.

Amaze is seeking a compassionate and skilled Nurse Practitioner (NP) or Physician Assistant (PA), to join our dedicated virtual care team. We welcome Advanced Practice Providers (APPs) who are driven by empathy, continuous learning, and delivering patient-first solutions in a flexible, on-demand environment.

Responsibilities

• Uncover root causes: Ask thoughtful, intuitive questions over video or secure chat to understand the underlying issues behind illness, injury, or medical conditions.

• Deliver accurate diagnoses: Utilize clinical expertise, patient history, and remote diagnostic tools to provide precise and informed assessments in a virtual setting.

• Guide care decisions: Efficiently order, interpret, and follow up on lab tests, leveraging digital platforms to personalize and coordinate each patient’s care plan.

• Prescribe with clarity: Electronically write prescriptions and clearly explain their proper usage, administration, and possible side effects, ensuring patients feel informed and confident through virtual or written communication.

• Collaborate as a team: Work closely with physicians, fellow APPs, and the extended care team to deliver seamless, coordinated care with a patient-first approach.

• Innovate under pressure: Respond to emerging challenges with creative, patient-centered solutions that adapt to the realities and opportunities of virtual care.

• Education & Licensure: Active, unrestricted license as an APP. NPs must hold a compact nursing license and be certified as a Family Nurse Practitioner (FNP).

• Experience: A minimum of five (5) years practicing independently managing patient care as an APP in a family, primary or urgent care setting.

• Virtual Care Experience: Experience using digital tools and platforms to deliver care in a virtual environment, including providing urgent virtual visits, chronic care follow-up, and mental health conversations in a patient-facing care setting.

• Care Coordination: Experience coordinating care plans with physicians and the broader care team.

• Key Attribute: Strong communication and digital literacy skills to connect with patients and team members alike in a virtual environment.

• Work Schedule: Four (4) - 10 hour days with rotating weekends. Current available shift is 12PM to 10PM MST.

• Language: While not required, candidates who are bilingual in English and Spanish are preferred.

• Location: While this is a virtual position, applicants must live in one of the following states: Arizona, Colorado, Florida, Ohio, or Texas.

Amaze provides an extensive benefits package featuring medical, dental, and vision coverage, along with paid time off and a 401(k) plan.

Pay Range is $55- $70/hr

Telix Pharmaceuticals is a dynamic, fast-growing radiopharmaceutical company with offices in Australia (HQ), Belgium, Japan, Switzerland, and the United States. Our mission is to deliver on the promise of precision medicine through targeted radiation. At our core, we exist to create products that seek to improve the quality of life for people living with cancer and rare diseases. You will be supporting the international roll-out of our approved prostate cancer imaging agent and helping us to advance our portfolio of late clinical-stage products that address significant unmet need in oncology and rare diseases.

See Yourself at Telix

Key Accountabilities:

Key Capabilities:

• Commitment to excellence: Take pride in your work and consistently strive for excellence in everything you do
• Results-oriented: Driven to achieve goals and objectives, with a strong focus on delivering measurable results
• Creativity and innovation: Possess a willingness to think outside the box and come up with unique and creative solutions to challenges
• Strong communication skills: Able to communicate effectively with colleagues and stakeholders at all levels, using clear and concise language
• Collaboration: Work effectively as part of a team, actively sharing knowledge and expertise to achieve common goals
• Resilience: Demonstrate the ability to bounce back from setbacks and persevere in the face of challenges
• Inclusive mindset: Demonstrate an understanding and appreciation for diversity, and actively work to create an inclusive environment where everyone feels valued and respected
• Adaptability: Comfortable working in a dynamic environment, able to adjust to changing priorities, and willing to take on new challenges
• Ethical behavior: Act with integrity and demonstrate a commitment to ethical behavior in all interactions with colleagues and stakeholders
• Continuous learning: Show a commitment to ongoing learning and professional development, continually seeking out opportunities to expand your knowledge and skills

At Telix, we believe everyone counts, we strive to be extraordinary, and we pursue our goals with determination and integrity. You will be part of an engaged and supportive group of colleagues who all have a shared purpose: to help people with cancer and rare diseases live longer, better quality lives. Being a Telix employee means being a part of a unique, global, interdisciplinary team working to deliver what’s next in precision medicine. We have hybrid and remote employees located all around the world. We offer competitive salaries, annual performance-based bonuses, an equity-based incentive program, generous vacation, paid wellness days and support for learning and development.

Telix Pharmaceuticals is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.

VIEW OUR PRIVACY POLICY HERE

[We show compassion to heal minds. ]🧠 About Legion HealthLegion Health is a technology-forward psychiatry company delivering world-class outpatient mental health care while expanding access for patients through insurance.

We’re expanding across Mexico, Brazil, Argentina, Colombia, Chile, and Peru, and we’re looking for an experienced Clinical Data Manager to help build the foundation of our growing LATAM Data Management...

DescriptionThe Senior Clinical Operations Manager (Sr.

Telix Pharmaceuticals is a dynamic, fast-growing radiopharmaceutical company with offices in Australia (HQ), Belgium, Japan, Switzerland, and the United States. Our mission is to deliver on the promise of precision medicine through targeted radiation. At our core, we exist to create products that seek to improve the quality of life for people living with cancer and rare diseases. You will be supporting the international roll-out of our approved prostate cancer imaging agent and helping us to advance our portfolio of late clinical-stage products that address significant unmet need in oncology and rare diseases.

See Yourself at Telix

The Associate Medical Director, Prostate Cancer Theranostics leads the execution of the US medical affairs plan across the prostate cancer theranostic portfolio, contributing to medical strategy, launch readiness, and lifecycle planning in partnership with the VP of Medical Affairs Americas. The role drives alignment of medical deliverables across Commercial, Clinical Operations, Marketing, Market Access, HEOR, Regulatory, Development, and other Medical Affairs partners. The Associate Medical Director develops and delivers core components of the medical plan, including medical education, advisory boards, podium and speaker content, investigator-initiated trial (IIT) strategy, clinical trial recruitment support, and scientific communications. As a subject-matter expert in prostate cancer radiopharmaceuticals and the prostate cancer patient journey, the role maintains current knowledge of publications, clinical trials, guidelines, and standards of care, and translates emerging data into recommendations for medical leadership.

Key Accountabilities:

• Lead execution of the US medical affairs plan for the prostate cancer theranostic portfolio, contributing to medical strategy, priorities, and the medical operating plan in partnership with the VP of Medical Affairs Americas.
• Drive cross-functional alignment with US Medical Affairs, Clinical Development, Commercial, Market Access, HEOR, Regulatory, Marketing, and Medical Information on medical deliverables and timelines.
• Contribute to medical affairs strategy for prostate cancer theranostic assets, including launch readiness and lifecycle planning, and lead integration of medical tactics and deliverables.
• Serve as a subject-matter expert on prostate cancer theranostics, providing scientific input into integrated medical planning, evidence gaps, and competitive landscape.
• Provide medical leadership on prostate cancer clinical protocol review, including recruitment strategy, data interpretation, investigator engagement, expanded access programs, clinical registries, and IIT protocol review.
• Develop and review scientifically accurate medical content, including podium presentation materials, speaker decks, medical education programs, advisory board content, symposia materials, and promotional/non-promotional resources through MLR review.
• Prepare and support internal and external speakers, ensuring scientific narrative, clinical context, competitive landscape, and use of data are clear, balanced, compliant, and aligned to medical strategy.
• Build and maintain scientific relationships with KOLs, investigators, and professional societies in prostate cancer theranostics.

Maintain current knowledge of prostate cancer radiopharmaceutical publications, clinical trials, treatment guidelines, patient journey dynamics, and competitive data, and translate implications into recommendations for medical leadership.

Education and Experience:

• Advanced degree (PhD, PharmD, MD) with prostate oncology experience required or equivalent experience.
• 8+ years of Medical Affairs experience, including experience leading cross-functional initiatives in oncology or specialty therapeutics
• Experience working with clinical operations, R&D and/or medical affairs.
• Deep expertise in prostate cancer radiopharmaceuticals, theranostics, imaging and therapy integration, and the prostate cancer patient journey preferred.
• Experience interpreting scientific data, market research, competitive intelligence, clinical utility evidence, and evolving clinical practice dynamics; proficient in Microsoft Office Suite.
• Demonstrated ability to contribute to medical strategy and lead cross-functional execution in a matrixed environment.
• Ability to interact externally and internally to support overall Company business strategy.
• Knowledge of clinical trial methodology, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols.
• Proven ability to collaborate effectively across matrixed teams and influence without direct reporting authority.
• Excellent verbal, written, and presentation communication skills, including development of medical content for scientific exchange, speaker preparation, and podium presentations.
• Demonstrated ability to develop and execute medical affairs tactical plans that incorporate lifecycle planning, competitive positioning, clinical utility, IIT, and clinical trial recruitment support.
• Commitment to staying abreast of critical publications, clinical trials, congress data, and guideline updates relevant to prostate cancer radiopharmaceuticals and theranostics.
• Detailed knowledge of regulations and compliance practices related to industry interactions with healthcare professionals.
• Experience building relationships with KOLs, investigators, and professional societies in oncology.
• Proven track record of delivering results that meet or exceed targeted objectives.
• Valid driver’s license.

Key Capabilities:

• Commitment to excellence: Take pride in your work and consistently strive for excellence in everything you do
• Results-oriented: Driven to achieve goals and objectives, with a strong focus on delivering measurable results
• Creativity and innovation: Possess a willingness to think outside the box and come up with unique and creative solutions to challenges
• Strong communication skills: Able to communicate effectively with colleagues and stakeholders at all levels, using clear and concise language
• Collaboration: Work effectively as part of a team, actively sharing knowledge and expertise to achieve common goals
• Resilience: Demonstrate the ability to bounce back from setbacks and persevere in the face of challenges
• Inclusive mindset: Demonstrate an understanding and appreciation for diversity, and actively work to create an inclusive environment where everyone feels valued and respected
• Adaptability: Comfortable working in a dynamic environment, able to adjust to changing priorities, and willing to take on new challenges
• Ethical behavior: Act with integrity and demonstrate a commitment to ethical behavior in all interactions with colleagues and stakeholders
• Continuous learning: Show a commitment to ongoing learning and professional development, continually seeking out opportunities to expand your knowledge and skills

At Telix, we believe everyone counts, we strive to be extraordinary, and we pursue our goals with determination and integrity. You will be part of an engaged and supportive group of colleagues who all have a shared purpose: to help people with cancer and rare diseases live longer, better quality lives. Being a Telix employee means being a part of a unique, global, interdisciplinary team working to deliver what’s next in precision medicine. We have hybrid and remote employees located all around the world. We offer competitive salaries, annual performance-based bonuses, an equity-based incentive program, generous vacation, paid wellness days and support for learning and development.

Telix Pharmaceuticals is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.

VIEW OUR PRIVACY POLICY HERE

Telix Pharmaceuticals is a dynamic, fast-growing radiopharmaceutical company with offices in Australia (HQ), Belgium, Japan, Switzerland, and the United States. Our mission is to deliver on the promise of precision medicine through targeted radiation. At our core, we exist to create products that seek to improve the quality of life for people living with cancer and rare diseases. You will be supporting the international roll-out of our approved prostate cancer imaging agent and helping us to advance our portfolio of late clinical-stage products that address significant unmet need in oncology and rare diseases.

See Yourself at Telix

The Associate Medical Director, Renal Cancer Theranostics leads the execution of the US medical affairs plan across the renal cancer theranostic portfolio, contributing to medical strategy, launch readiness, and lifecycle planning in partnership with the VP of Medical Affairs Americas. The role drives alignment of medical deliverables across Commercial, Clinical Operations, Marketing, Market Access, HEOR, Regulatory, Development, and other Medical Affairs partners. The Associate Medical Director develops and delivers core components of the medical plan, including medical education, advisory boards, podium and speaker content, investigator-initiated trial (IIT) strategy, clinical trial recruitment support, and scientific communications. As a subject-matter expert in renal cancer radiopharmaceuticals and the renal cancer patient journey, the role maintains current knowledge of publications, clinical trials, guidelines, and standards of care, and translates emerging data into recommendations for medical leadership.

Key Accountabilities:

• Lead execution of the US medical affairs plan for the renal cancer theranostic portfolio, contributing to medical strategy, priorities, and the medical operating plan in partnership with the VP of Medical Affairs Americas.
• Drive cross-functional alignment with US Medical Affairs, Clinical Development, Commercial, Market Access, HEOR, Regulatory, Marketing, and Medical Information on medical deliverables and timelines.
• Contribute to medical affairs strategy for renal cancer theranostic assets, including launch readiness and lifecycle planning, and lead integration of medical tactics and deliverables.
• Serve as a subject-matter expert on renal cancer theranostics, providing scientific input into integrated medical planning, evidence gaps, and competitive landscape.
• Provide medical leadership on renal cancer clinical protocol review, including recruitment strategy, data interpretation, investigator engagement, expanded access programs, clinical registries, and IIT protocol review.
• Develop and review scientifically accurate medical content, including podium presentation materials, speaker decks, medical education programs, advisory board content, symposia materials, and promotional/non-promotional resources through MLR review.
• Prepare and support internal and external speakers, ensuring scientific narrative, clinical context, competitive landscape, and use of data are clear, balanced, compliant, and aligned to medical strategy.
• Build and maintain scientific relationships with KOLs, investigators, and professional societies in renal cancer theranostics.

Maintain current knowledge of renal cancer radiopharmaceutical publications, clinical trials, treatment guidelines, patient journey dynamics, and competitive data, and translate implications into recommendations for medical leadership.

Education and Experience:

• Advanced degree (PhD, PharmD, MD) with renal oncology experience required or equivalent experience.
• 8+ years of Medical Affairs experience, including experience leading cross-functional initiatives in oncology or specialty therapeutics
• Experience working with clinical operations, R&D and/or medical affairs.
• Deep expertise in renal cancer radiopharmaceuticals, theranostics, imaging and therapy integration, and the renal cancer patient journey preferred.
• Experience interpreting scientific data, market research, competitive intelligence, clinical utility evidence, and evolving clinical practice dynamics; proficient in Microsoft Office Suite.
• Demonstrated ability to contribute to medical strategy and lead cross-functional execution in a matrixed environment.
• Ability to interact externally and internally to support overall Company business strategy.
• Knowledge of clinical trial methodology, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols.
• Proven ability to collaborate effectively across matrixed teams and influence without direct reporting authority.
• Excellent verbal, written, and presentation communication skills, including development of medical content for scientific exchange, speaker preparation, and podium presentations.
• Demonstrated ability to develop and execute medical affairs tactical plans that incorporate lifecycle planning, competitive positioning, clinical utility, IIT, and clinical trial recruitment support.
• Commitment to staying abreast of critical publications, clinical trials, congress data, and guideline updates relevant to renal cancer radiopharmaceuticals and theranostics.
• Detailed knowledge of regulations and compliance practices related to industry interactions with healthcare professionals.
• Experience building relationships with KOLs, investigators, and professional societies in oncology.
• Proven track record of delivering results that meet or exceed targeted objectives.
• Valid driver’s license.

Key Capabilities:

• Commitment to excellence: Take pride in your work and consistently strive for excellence in everything you do
• Results-oriented: Driven to achieve goals and objectives, with a strong focus on delivering measurable results
• Creativity and innovation: Possess a willingness to think outside the box and come up with unique and creative solutions to challenges
• Strong communication skills: Able to communicate effectively with colleagues and stakeholders at all levels, using clear and concise language
• Collaboration: Work effectively as part of a team, actively sharing knowledge and expertise to achieve common goals
• Resilience: Demonstrate the ability to bounce back from setbacks and persevere in the face of challenges
• Inclusive mindset: Demonstrate an understanding and appreciation for diversity, and actively work to create an inclusive environment where everyone feels valued and respected
• Adaptability: Comfortable working in a dynamic environment, able to adjust to changing priorities, and willing to take on new challenges
• Ethical behavior: Act with integrity and demonstrate a commitment to ethical behavior in all interactions with colleagues and stakeholders
• Continuous learning: Show a commitment to ongoing learning and professional development, continually seeking out opportunities to expand your knowledge and skills

At Telix, we believe everyone counts, we strive to be extraordinary, and we pursue our goals with determination and integrity. You will be part of an engaged and supportive group of colleagues who all have a shared purpose: to help people with cancer and rare diseases live longer, better quality lives. Being a Telix employee means being a part of a unique, global, interdisciplinary team working to deliver what’s next in precision medicine. We have hybrid and remote employees located all around the world. We offer competitive salaries, annual performance-based bonuses, an equity-based incentive program, generous vacation, paid wellness days and support for learning and development.

Telix Pharmaceuticals is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, and other legally protected characteristics.

VIEW OUR PRIVACY POLICY HERE

OverviewDane Street is seeking an experienced, licensed Speech-Language Pathologist (SLP) to join our growing team of expert clinical reviewers.

[We show compassion to heal minds. ]🧠 About Legion HealthLegion Health is a technology-forward psychiatry company delivering world-class outpatient mental health care while expanding access for patients through insurance.

[We show compassion to heal minds. ]🧠 About Legion HealthLegion Health is a technology-forward psychiatry company delivering world-class outpatient mental health care while expanding access for patients through insurance.