Handle inbound and outbound calls to support healthcare professionals during recall projects, providing accurate and timely information.
Manage and maintain recall project documentation, ensuring all records are updated and compliant with industry standards.
Monitor recall progress and coordinate communications between teams to ensure effective resolution of product issues.
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. With a diverse workforce worldwide, we foster a culture of inclusion, belonging, and continuous innovation.
Perform copy-edit and translation tasks on clinical and regulatory documents for assigned projects.
Manage language resources, resolve terminology queries, and coordinate with freelancers and internal teams.
Ensure high-quality linguistic deliverables, meet KPIs, and contribute to process improvements.
Welo Life Sciences is a specialized language and technology partner serving pharmaceutical, CRO, and medical device organizations in regulated global markets. They deliver ISO-certified translation, linguistic validation, and localization solutions with a secure, audit-ready framework.
Provide virtual or telephonic support to clients and healthcare professionals, documenting medical information requests and adverse events.
Conduct study compliance calls and enroll participants in educational seminars.
Maintain excellent quality and productivity standards while adhering to program scripts and guidelines.
Inizio Engage is a strategic, commercial and creative engagement partner specializing in healthcare. They employ over 7,000 experts in more than 20 countries, fostering a passionate, diverse, and global culture that challenges conventional thinking to improve health outcomes.
Leads writing and preparing clinical and regulatory documents for drug and device development.
Coordinates review, approval, and quality control across functions to ensure compliance and timelines.
Develops knowledge of US and international regulations and participates in process improvements.
AbbVie discovers and delivers innovative medicines and solutions addressing serious health issues in immunology, oncology, neuroscience, and aesthetics. They are a large global biopharmaceutical company committed to having a remarkable impact on people's lives.
Produce high-quality content for diverse medical communications projects, demonstrating excellent scientific understanding.
Develop content with minimal supervision, within budget and on time, using client approval systems.
Attend conferences, present work to clients, and manage day-to-day client communication and relationships.
Lumanity is dedicated to improving health outcomes by accelerating and optimizing access to life-changing medicines. As a global strategic partner, they bring together strategy, evidence, engagement, and technology to engineer breakthrough value.
Lead authoring and development of high-complexity Phase II-IV clinical regulatory documents for a top pharma partner.
Own the end-to-end medical writing process from planning through final delivery, ensuring alignment with strategy and timelines.
Coordinate cross-functional teams across geographies and facilitate comment resolution to drive document development.
Fortrea delivers solutions that bring life-changing treatments to patients faster. They are a global organization that empowers employees to shape their own career path with comprehensive training and management support.
Write clear and concise medical copy for HCPs and patients, adhering to ABPI guidelines and quality processes.
Collaborate with strategy, creative, and account teams to develop effective campaigns.
Manage projects from concept to completion, ensuring timelines and quality standards.
Real Chemistry is a global healthcare communications and marketing agency that partners with top pharmaceutical and biotech companies. The company fosters a culture of innovation and collaboration, with over 5 years of growth, and has been certified as a Great Place to Work.
Process individual case safety reports (ICSRs) for clinical trials and post-marketing programs.
Ensure accurate data entry, coding, and query resolution in the Argus Safety Database.
Collaborate with cross-functional teams to meet regulatory reporting requirements and maintain compliance.
Precision Medicine Group is a global life sciences company specializing in precision medicine and drug development services. They employ thousands of professionals and emphasize a collaborative culture.
Develop medical affairs and publications content across multiple workstreams, ensuring high scientific quality and credibility.
Create materials tailored for different medical audiences with minimal internal review, demonstrating excellent quality control.
Collaborate with clients to ensure projects meet strategic marketing and medical needs, maintaining a client-centric attitude.
ApotheCom is a leader in medical communications, part of Inizio, a global healthcare consulting and communications group. With over 12,000 employees globally, Inizio creates compelling content and engages communities to achieve outcomes that matter.
Coordinate and organize webinars, trainings, presentations, and critical incident interventions for clients across multiple European countries.
Collaborate with internal and external stakeholders, including the international headquarters in England/South Africa.
Ensure quality control of training materials and provide administrative support via chat and email.
Lyra Health is the leading provider of mental health solutions for employers, serving over 20 million people globally. The company has delivered millions of care sessions and is known for its transformative care model.
Establish and maintain scientific partnerships with Key Opinion Leaders in oncology, rheumatology, and immunology.
Provide non-promotional scientific discussions on biosimilars including mechanism of action, safety, and efficacy.
Contribute to medical strategy by generating insights and supporting launch readiness.
Dr. Reddy's Laboratories is a global pharmaceutical company providing innovative and affordable healthcare solutions, from prescription generics to biopharmaceuticals. The subsidiary fosters a diverse, inclusive, and collaborative culture committed to sustainability and patient health.
Translate pharmacovigilance content from Farsi (fas-IR) to English (en-GB and en-US).
Perform copy editing and machine translation post-editing (MTPE) to ensure high-quality deliverables.
Maintain adherence to deadlines and project requirements using proprietary systems and CAT tools.
Welocalize is a global localization and translation company providing language services including translation, localization, and QA testing. They work with a worldwide network of freelancers and agencies, offering opportunities on critical medical and clinical content.
Author clinical study reports, protocols, informed consent forms, narratives, and investigator brochures across therapeutic areas.
Represent Medical Writing at meetings, drive document development, and articulate strategy and timelines.
Mentor junior staff, manage multiple priorities, and foster collaboration to resolve conflict.
Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led for over 30 years by physician-scientists, the company has a fast-growing, science-driven culture and is recognized as a Great Place to Work in 2021, among other awards.
Translate and validate medical content for the Burmese market, focusing on patient records and clinical protocols.
Ensure compliance with regulatory standards, including GxP environments and ISO 17100 quality standards.
Work as a 1099 contractor with flexible hours, supplementing income through diverse, impactful projects.
LILT is transforming global communication by providing multilingual AI and human-verified services to Enterprises, Governments, and AI Developers. They are a global community of linguists, subject matter experts, and language professionals advancing human knowledge together.
Develop and review medical response documents with scientific accuracy and editorial excellence.
Perform source-to-output verification, validate references, and ensure consistency across deliverables.
Support MLR readiness through quality checks aligned with FDA guidance, AMA style, and ICMJE standards.
EVERSANA creates next-generation commercialization services for the life sciences industry. Their global team of over 6,000 employees serves more than 670 clients, from biotech start-ups to pharmaceutical companies, and embraces diversity and inclusion.
Develop safety management plans and oversee serious adverse event case management from intake to regulatory reporting.
Perform intake, triage, data entry, medical coding, and narrative composition for individual case safety reports.
Provide safety training, review standard operating procedures, and assist clients with safety-related reviews.
Precision Medicine Group is a global contract research organization specializing in clinical research and drug development services. The company fosters a collaborative culture and offers competitive benefits to support employee growth.