Create clinical practice questions and explanations for OB/Gyn series. Edit questions for accuracy, readability, and educational value. Collaborate with medical illustration team and attend team meetings. Terminal medical degree and question writing experience required.

Translate and edit Thai into English content for Clinical Research & Pharmacy documents. Use CAT tool XTM. Minimum 2 years' experience in translation/editing. Quick response times and attention to detail required.

Translate Armenian medical documents into English with attention to detail and quick response times. Use CAT tools and have at least 2 years of experience in medical/pharmaceutical documents. Freelance/Independent Contract with steady volume of projects.

Translate medical documents from English to Armenian using CAT tools. Requires degree or 5 years of translation experience, excellent knowledge of both languages, and 2 years of experience in investigator-facing, patient-facing, and/or pharmacy material. Freelance with steady volume and on-time payments.

Lead the creation and maintenance of medical information resources and support content development. Provide guidance to the Medical Information Call Center staff. Collaborate with business partners to support informational needs and strategies.

Lead the development and execution of medical affairs strategy and programs for Solid Tumors in Europe and International regions. Provide medical insights to regional development teams, ensure compliance with regulations, and establish external relationships with KOLs.

Develop and lead evidence generation plan, facilitate scientific engagements, align and implement medical communications strategy, provide strategic direction for study design and delivery, and enable access to medicines through education and partnerships.

Curate and tag medical insights, ensure quality, act on customer requests, specialize in a therapeutic area. Requires medicine/life sciences degree, fast learning, good ethics, strong English communication. Nice to have manual development and stakeholder management experience.

Curate and tag medical insights notes, ensure high-quality output, act on customer requests, and specialize in a therapeutic area. University degree in medicine or life sciences and strong communication skills required.

Curate and tag medical insights notes, ensure high-quality output, act on customer requests, specialize in a therapeutic area. Academic background in medicine or life sciences required. Fast-paced, remote work environment.

Perform telephonic outreach to patients, coordinate with practice contacts, navigate through electronic systems, and follow company policies. Must be a Certified Medical Assistant with strong computer skills.

Offer medical guidance for post-marketing efforts, handle regulatory submissions, oversee global clinical trials, and deliver scientific education on products to field-based staff and customers in North America.

Assess medical care quality, collaborate with patient experience teams, reduce conflict, increase patient satisfaction, manage clinical experience team, assist in timely completion of clinical tasks, serve as collaborating/supervising physician, communicate with team members and patients.

The Medical Director will serve as the primary medical lead for clinical trials, including strategy, design, and execution. They will also monitor the safety of enrolled subjects and collaborate with cross-functional teams for efficient study execution.

Provides medical oversight of clinical trials, attends meetings, consults with clients, investigators, and project team members. Manages medical aspects of tasks across the product life-cycle, monitors safety variables, reviews adverse events, and contributes to label updates.

Evaluate medical records, identify trends in coding practices, educate staff on proper coding techniques, coordinate with medical professionals for quality patient care. 2+ years of experience and professional medical coding certification required. $20-35/hr compensation. Full benefits.

Lead the medical policy committee, develop client relationships, and present payment policies. Serve as a clinical liaison with health plan clients and support sales activity. Requires MD/DO and health plan experience.

Lead the design of the Global Medical Strategy for all Therapeutic Areas and Products. Develop and own the Integrated Evidence Plan for all products. Actively participate in Investigator Sponsored Trials and Compassionate Use decision making.

Editorial lead for clinical guidelines across various specialties. Manage the content pipeline for clinical specialties. Create and enforce processes for developing, maintaining, and communicating medical policy and provider facing content.

Serving as the medical point person on assigned accounts, developing and writing medical content for various therapeutic areas, managing a team of writers, and collaborating with internal teams and clients.

Provide medical oversight, leadership, and accountability for the efficiency, quality, and performance of medical conduct within a region. Manage staff, support study implementation, and ensure compliance with regulations and guidelines.

Assist in developing and implementing educational programming for clinical audiences. Coordinate with subject-matter experts, communicate with stakeholders, and analyze program impact. Maintain program records and manage program budgets. Identify new opportunities for clinician engagement.

Responsible for ensuring clinical excellence, driving product innovation, and providing leadership and strategic direction. Develop and implement clinical service models, oversee product development, and drive business performance to meet organizational goals.

Establish Relationships and a Safe Learning Environment, Deliver Excellent and Engaging Synchronous Sessions, Demonstrate Fluent Use of Your Teaching Tools, Communicate and Provide Feedback Frequently

Develop relationships with healthcare professionals, provide scientific information, respond to medical presentation requests, plan territories, mentor MSLs, assist with investigator-sponsored trials, and contribute to internal training and communication.

Review medical claims, analyze based on coding guidelines, identify process improvements, collaborate with internal departments, support provider appeals. 3+ years medical bill coding and CPC, RHIT, or RHIA certification required.

Recruit, train, develop, and manage a team of high-performing MSLs. Provide strategic direction for MSL development and execution of comprehensive territory medical plans. Develop relationships with healthcare professionals and provide them with credible, scientific information.

Provide evidence-based medical reviews for patient care, conduct physician consultation calls, recommend alternative services or treatments, collaborate with healthcare providers and stay current on healthcare regulations and industry developments.

Provide evidence-based medical reviews for patient care, conduct physician consultation calls, recommend alternative treatments, collaborate with healthcare providers, and stay current on healthcare regulations and industry developments.

Receiving and vetting medical claims, interpreting documentation, and determining payment eligibility. Providing customer support and recommendations to management. Working 40 hours per week under moderate supervision.

An experienced Medical Coding Specialist is required to independently perform analysis of claims, review medical records, and ensure coding is correct according to guidelines. They must be passionate about helping older adults live fulfilling lives in their home.

Develop and maintain coding accuracy thresholds, review medical records, conduct analysis, collaborate with teams, provide coding education. AAPC/AHIMA certification and healthcare consulting experience preferred. Salary range: $100k-$160k USD.

Develop relationships with healthcare professionals, provide scientific information, attend conferences, collaborate with researchers. Become a therapeutic area expert, identify potential investigators and research projects, participate in scientific dialogue.

Develop relationships with healthcare professionals, provide credible scientific information, address safety and off-label use questions, create a medical plan, become a therapeutic area expert, and identify potential investigators and research projects.

Responsible for building relationships with healthcare professionals, providing medical information, developing territory plans, and becoming a therapeutic area expert. Assist in identifying potential investigators and contribute to internal training and communication.

Communicate medical and scientific information to healthcare professionals, develop a comprehensive territory medical plan, attend conferences, and identify potential investigators and research projects. Travel required.

Assign accurate codes to patient records using ICD-9-CM, ICD-10-CM, and ICD-10-PCS codes. Sequence codes accurately based on medical record documentation. Communicate coding issues to appropriate personnel for follow up and resolution.

Provide clinical/scientific knowledge for the development and communication of the evidence generation plan. Support cross-functional collaborations and provide clinical input for safety and regulatory interactions. Author clinical study reports, publications, and regulatory submissions.

Direct and oversee clinical studies at multiple phases of clinical development. Inspire a cross-functional team to promote high performance. Provide medical and scientific input in review of clinical data. Lead cross-functional teams focusing on clinical development strategy.

Write high-quality, strategically aligned medical writing deliverables, author regulatory documents, and ensure communication consistency across program documentation. Participate in global teams and interact with regulatory agencies, and possibly manage writers.

Create medical publications adhering to industry standards. Lead projects, coordinate submissions, and mentor junior colleagues. Provide guidance to authoring teams and manage document reviews. PhD, MD, MPH, or PharmD required with 7+ years of experience as a medical writer.

Create medical publications following industry guidelines. Lead projects, collaborate with experts, and mentor junior colleagues. Coordinate journal submissions and adhere to publication policies and procedures.

Review medical records, verify outpatient behavioral health service documentation for compliance with coding guidelines and regulations. Monitor coding trends, recommend process improvements, maintain accurate documentation, and participate in quality improvement initiatives.

Ensure quality control of clinical regulatory documents by conducting independent reviews, verifying data and content, checking consistency, and adhering to guidelines. Collaborate with writers and oversee CRO/vendor activities.

Spending the majority of your time reviewing medical records to ensure correct diagnosis and procedure codes, performing audits for accuracy, preparing reports, providing coding insights and education, and tracking coding and billing rules.

Responsible for managing the educational representatives and inside sales representatives. Prepare sales forecasts, monitor calls, and collaborate with leaders to meet sales targets. Improve processes and increase customer engagement.

Manage project teams in drafting report specifications, medical writing, and coordinating regulatory submissions. Prepare key clinical documents for regulatory submissions and oversee external vendors for writing service.

Monitor and respond to patient communications using a digital platform, follow clinical protocols to inform patients of lab results and next steps, assist with referrals and patient forms, provide outreach and follow-up for patient care.

Review Medicare and Medicaid claims for accuracy and compliance. Submit patient care reports to government payers. Handle high volume of claims daily. Preferred medical background: LPN, RN, EMT, Paramedic.