Building strong, credible relationships with key scientific and clinical experts.
Leading scientific discussions and delivering engaging educational presentations.
Supporting clinical research, real-world evidence generation, and publication activities.
AbbVie is a global biopharmaceutical company that discovers and delivers innovative medicines in immunology, oncology, neuroscience, and aesthetics. With a collaborative culture and a commitment to transforming lives, the company operates as an equal opportunity employer.
Serve as the primary scientific contact for investigators, facilitating scientific dialogue and supporting AbbVie's clinical trials with pipeline assets.
Establish and maintain collaborative relationships with thought leaders and key institutions to advance research and development.
Deliver credible scientific presentations and provide medical and scientific field intelligence to inform internal strategies.
AbbVie discovers and delivers innovative medicines and solutions for serious health issues in immunology, oncology, neuroscience, and aesthetics. It is a large global biopharmaceutical company committed to integrity, innovation, and transforming lives.
Clinically check prescriptions accurately and efficiently using the online pharmacy platform.
Ensure prescriptions are reviewed and progressed within agreed SLAs and turnaround times.
Maintain consistent checking volumes without compromising clinical accuracy or patient safety.
Montu UK is a leading digital health company specialising in cannabis-based medicines, committed to transforming lives by improving access to safe treatments. They offer a dynamic, collaborative, and supportive working environment.
Lead execution of Medicaid contracts with PBMs, coordinating with Marketing, Finance, and Area Access teams.
Serve as subject matter expert for Medicaid legislation and develop strategies balancing patient access and business goals.
Proactively identify risks and opportunities, and build standardized dashboards to ensure contract compliance.
AbbVie discovers and delivers innovative medicines and solutions to address serious health issues across immunology, oncology, neuroscience, and aesthetics. As a large global biopharmaceutical company, they foster a collaborative culture focused on innovation and patient impact.
Lead a 6-person MSL team in Plastics & Regenerative Medicine while maintaining a personal field territory.
Ensure scientific engagement plans align with brand strategy and medical objectives.
Provide coaching, training, and performance management to the MSL team.
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. The company operates globally in immunology, oncology, neuroscience, and aesthetics.
Oversee content compliance review for marketing, educational, and communications materials, ensuring alignment with pharmacy regulations and FDA/FTC guidelines.
Collaborate cross-functionally with Compliance, Clinical, Marketing, and Legal teams to provide risk-based guidance and streamline content approval workflows.
Develop training resources, manage review queues in Asana, and maintain auditable documentation to support compliance and process improvement.
Strive Pharmacy is a personalized compounding pharmacy focused on individualized care, creating medications tailored to each patient's needs. The company is growing and fosters a culture of community and professional development, with team events and a commitment to employee growth.
Ensure product safety and legality by providing consultancy on legal and technical compliance, specification interrogation, pack copy generation, and artwork approval.
Prepare and check pack copy adhering to UK and EU legislation, and liaise with clients, suppliers, design agencies, and print houses.
Maintain technical competence, share knowledge with colleagues, and attend internal and external meetings as required.
SGS is the world's leading testing, inspection and certification company, recognized as a global benchmark for sustainability, quality, and integrity. With 100,000 employees operating a network of 2,600 offices and laboratories, they enable a better, safer, and more interconnected world through trust and reliability.
Provide scientific and medical direction to integrate clinical relevance into client brand strategies.
Monitor disease categories and product labeling to derive actionable insights for medical strategy.
Support senior Medical staff in new business and thought leadership while training junior team members.
Inizio Evoke is a healthcare communications agency that aims to make health more human through strategic and creative work. They foster an inclusive, authentic culture and offer flexible work environments with a focus on collaboration and professional growth.
Provide strategic regulatory input and manage European Clinical Trial Applications (CTA) and amendments.
Serve as key regulatory liaison for multi-continental oncology projects, collaborating with cross-functional teams.
Maintain expertise in GCP, EU regulations, and support business development activities.
Theradex Oncology is a full-service CRO specializing in early and late-phase oncology trials globally. Founded in 1982 with over 40 years of experience, the company has managed more than 250 trials and partners with the National Cancer Institute, maintaining a focused culture on cancer drug development.
Independently plans and prepares regulatory documents and medical communications for all phases of product development.
Organizes, analyzes, interprets, and presents scientific and statistical information per ICH guidelines.
Collaborates with cross-functional internal and external document production teams.
Veristat is a global contract research organization with over 30 years of expertise accelerating life-changing therapies to patients worldwide. The company has a flexible, inclusive culture with a 70% remote workforce and 66% women-led teams.
Serve as a key scientific resource providing accurate and timely medical information in response to unsolicited inquiries from healthcare professionals and patients.
Manage Medical Information operations, including system oversight, vendor coordination, and process optimization.
Collaborate cross-functionally with Medical Affairs, Pharmacovigilance, Regulatory, and Commercial teams to ensure compliant dissemination of medical information.
Cogent Biosciences is a publicly traded biotechnology company developing novel precision therapies for patients with unmet medical needs. We foster a collaborative environment with a focus on teamwork and innovation.
Independently plans and prepares regulatory documents and medical communications to support all phases of product development.
Organizes, analyzes, interprets, and presents scientific and statistical information in accordance with industry guidelines (ICH, ICMJE, GPP).
Collaborates with cross-functional internal and external teams under direction of Medical Writing management.
Veristat is a global contract research organization that accelerates life-changing therapies to patients worldwide. With over 30 years of expertise, the company has supported more than 105 approved therapies and fosters a flexible, inclusive culture with 70% remote workforce and 66% women-led teams.
Review 15 patient questionnaires per hour, preparing detailed cases for GP review.
Keep up to date with NICE guidelines on weight management and obesity treatment.
Maintain accurate patient records in line with data protection (GDPR) and refer patients appropriately.
We provide nationwide healthcare services for individuals, businesses, and the NHS, harnessing technology to deliver better local access to healthcare. We are a multidisciplinary team led by an NHS GP, dedicated to combating health inequalities through innovation and collaboration.
Provide clinical leadership and medical oversight for audit programs involving governmental and commercial payer claims.
Evaluate medical necessity, level of care, coding accuracy, and documentation sufficiency using payer policies and clinical standards.
Support audit methodologies, clinical validation frameworks, and quality assurance to ensure regulatory alignment and defensibility.
Machinify is a leading healthcare intelligence company delivering value, transparency, and efficiency to health plan clients. Deployed by over 85 health plans representing more than 270 million lives, they bring an AI-powered platform alongside best-in-class expertise.
Provide medical information responses to healthcare professionals and patients, including triaging drug information inquiries and disseminating responses verbally or in writing.
Identify and intake adverse events and product quality complaints, ensuring compliance with client SOPs and regulatory requirements.
Utilize drug information skills to critically evaluate medical literature and develop written correspondence for healthcare professionals.
EVERSANA provides next-generation commercialization services to the life sciences industry. With a global team of over 6,000 employees, we are committed to creating a healthier world and embracing diversity.
Act as the quality and compliance gate for all creative assets before they reach client Medical, Legal, and Regulatory review.
Own Veeva Vault PromoMats operations including annotations, claims management, and 2253 submission filing.
Enforce brand and design standards, review copy for accuracy, and maintain QA process documentation.
Power Digital is a tech-enabled growth firm at the intersection of marketing, consulting, and data intelligence, igniting revenue for leading companies. They are a people-first firm with a scalable brand and culture, managing billions in media with a dynamic team of consultative marketers and analysts.
Serve as primary physician reviewer for Utilization Management (UM) cases, advising other reviewers and attending daily calls with health plan teams.
Establish 2-3 cases per day for up to 6 markets, ensuring attendance on health plan calls and weekly meetings.
Participate in Process and Quality improvement in delegated Utilization Management, utilizing excellent analytical and deductive reasoning skills.
ChenMed is a family-owned, physician-led primary care provider focused on improving healthcare for moderate-to-low-income seniors. The company is rapidly expanding, with a culture of innovation, kindness, and making a difference.
Lead the preparation of complex clinical and regulatory documents including Clinical Study Protocols, Clinical Study Reports, and Investigator Brochures.
Collaborate with clinical development teams and stakeholders to produce accurate, compliant, and scientifically robust documentation.
Manage document timelines, review cycles, and project deliverables while ensuring quality standards and regulatory requirements are met.
Our partner is a specialized medical writing team supporting the development of high-quality regulatory documentation for the global pharmaceutical industry. It offers a collaborative, remote environment focused on quality, precision, and scientific communication.
Lead the development of disease-state and product-specific materials and the omni-channel scientific communications strategy.
Oversee the development of standard and custom responses to unsolicited requests and create internal Medical Information resources.
Lead publication strategy and execution for clinical and nonclinical data including manuscripts, abstracts, posters, and presentations.
Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines to target hypertension and related comorbidities. The company is fully remote and headquartered in Radnor, Pennsylvania.
Coordinate and track international regulatory submissions for IVD products in the EMEA region.
Manage regulatory release of products using the GTS tool and ensure compliance with IVD/medical device regulations.
Collaborate with global teams to document regulatory assessments and oversee channel partner licenses and renewals.
Agilent provides life science, diagnostic and applied market laboratories with instruments, services, consumables, applications and expertise. With 18,000 employees worldwide, the company fosters a culture of trust, respect, integrity, and inclusivity.