Lead and support Eli’s scientific publishing efforts.
Draft, edit, and prepare scientific documents for submission.
Work closely with Eli’s Medical Director and senior clinicians/scientists.
Eli Health is making continuous hormone monitoring possible so users can support their daily and long-term health. They are a small team of fewer than 20 people, where employees drive their own work and think creatively to solve open-ended problems.
Pfizer is dedicated to improving healthcare and transforming lives through innovative therapies. As a global company, they foster a culture of individual ownership and are committed to making the world a healthier place.
Manage the development and submission of grant proposals and contracts.
Design and develop major program components for proposed projects.
Support scientific manuscript writing and data analysis for publication.
Oregon Health & Science University (OHSU) is committed to anti-racism and social justice. It is an equal opportunity, affirmative action organization that values a diverse and culturally competent workforce.
Ensures complete study scoping, including testing requirements, facilities and other nuances.
Provides technical details to study team for study designs and updates.
Conducts investigations and assists with implementation of corrective actions, as needed.
ACM Global Laboratories impacts patients and their families by being purposefully patient-driven. Their dedication is reflected in the high-quality work provided by their teams every day around the globe.
Develop and maintain relationships with healthcare professionals within the assigned territory
Lead scientific conversations focused on disease understanding and research methodology
Collect and communicate medical insights from the field to internal stakeholders
Compass Pathways plc is a biotechnology company dedicated to accelerating patient access to evidence-based innovation in mental health. They are pioneering a new paradigm for treating mental health conditions focused on rapid and durable responses.
Support Dosing Program Lead across assets and may serve as dosing program representative on clinical trial teams
Contribute to the writing and editing of clinical study protocols, clinical study reports, manuscripts, and other study-related documents
Contribute to ongoing data review and cleaning, data summarization and analysis in support of abstracts, manuscripts and presentations for external meetings and conferences
Definium Therapeutics, formerly known as Mind Medicine, is a clinical stage biopharmaceutical company developing novel product candidates to treat brain health disorders. Founded in 2019, they are continuously expanding their presence and global footprint with a team of patient-centric, intelligent individuals.
Lead the preparation and review of clinical study reports, protocols, and other regulatory documents.
Perform medical writing tasks of high complexity and critical importance to ongoing projects.
Collaborate with cross-functional teams to gather and synthesize information for document development.
Jobgether uses an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. They identify the top-fitting candidates, and this shortlist is then shared directly with the hiring company.
Lead and develop a high-performing MSL team within a region, setting clear expectations for scientific excellence, compliance, and professional growth
Translate medical strategy into effective field execution, ensuring consistent, high-quality scientific engagement across territories
Ensure the timely collection, synthesis, and communication of actionable medical insights from the field to inform clinical development, medical strategy, and education planning
Compass Pathways plc is a biotechnology company dedicated to accelerating patient access to evidence-based innovation in mental health. They are pioneering a new paradigm for treating mental health conditions focused on rapid and durable responses through the development of their investigational COMP360 synthetic psilocybin treatment.
Align with business, clinical, and technology stakeholders to identify initiatives that drive significant business value.
Assist in developing contracts, statements of work, targeted proposals, and detailed responses to RFPs.
Manage the intake of client requests and assist in developing proposals with detailed timelines and budgets.
EVERSANA delivers next-generation commercialization services to the life sciences industry, serving over 650 clients from innovative biotech start-ups to established pharmaceutical companies. With over 7,000 employees globally, they foster an inclusive culture that values diversity and collaboration to improve patient lives.
Collect and interpret information from the Protocol, business development sold strategy & site feasibility team to prepare the site staff for site evaluation visits.
Oversee the execution of Site Activation, site activation strategy, adhering to project timelines.
Lead the process of study start-up to support site evaluation/selection visits on each new study and help get selected sites successfully activated and ready to consent.
Care Access is dedicated to making the future of health better for all by bringing world-class research and health services directly to communities. With hundreds of research locations, mobile clinics, and clinicians across the globe, they focus on ensuring every person has the opportunity to understand their health and access the care they need.
Maintain deep scientific knowledge on Kyowa Kirin therapy areas and data.
Foster relationships with Key External Experts to enhance their understanding of our science.
Respond to HCP inquiries and provide internal training on science and publications.
Kyowa Kirin International (KKI) is an inclusive pharmaceutical company. They focus on drug discovery and development, embedding care into their work to positively impact patients, families, and healthcare professionals, striving to deliver life-changing solutions. Their culture emphasizes teamwork, commitment to life, innovation, and integrity, aimed at creating a brilliant work environment.
Develop and maintain scientifically grounded relationships with healthcare professionals, researchers, and thought leaders.
Lead in-depth, compliant scientific conversations focused on disease understanding, research methodology, and emerging evidence.
Collect, analyze, and communicate medical insights from the field to internal stakeholders to inform clinical development, medical strategy, and educational planning.
Compass Pathways plc is a biotechnology company dedicated to accelerating patient access to evidence-based innovation in mental health. They focus on developing novel treatments that have the potential to improve the lives of those who are suffering with mental health conditions and who are not helped by current treatments.
Serve as a subject-matter expert on global clinical and regulatory writing projects
Lead the writing, review, and coordination of complex documents such as CTD Modules, Clinical Study Protocols, and Clinical Study Reports
Drive development of key clinical documents that align with overall program and submission strategy
Jobgether is a company that uses AI-powered matching to ensure applications are reviewed quickly, objectively, and fairly. Their system identifies the top-fitting candidates and shares this shortlist directly with the hiring company.
Execute patient-focused research studies from kickoff through closeout with senior oversight.
Collaborate closely with internal teams to remove friction and keep projects moving efficiently.
Support client communications, status updates, and documentation with professionalism and accuracy.
Konovo is a global healthcare intelligence company transforming research through technology, enabling faster, better, connected insights. With a workforce of over 200 employees across 5 countries, they collaborate to support some of the most prominent names in healthcare and are transitioning from a service-oriented model to a product-driven platform.
Assisting in the management of cross-functional sub teams to facilitate timely planning, execution, tracking, and completion of NDA-related clinical deliverables.
Setting up meetings, drafting agendas and detailed minutes, and tracking actions through completion.
Assisting in the identification of issues impacting plan execution and working with the team to identify risks and develop mitigation strategies
Amylyx is dedicated to ushering in a new era for treating diseases with high unmet needs. They value urgency, rigorous science, and unwavering commitment, demonstrated by their experienced team ready to take action.
Responsible for delivery of site activation readiness within the assigned country/sites.
Preparation of Clinical Trial Application Forms and submission dossier for submission to CA, EC, and other applicable local bodies.
Act as SME for collection and maintenance of site level critical path to Site Activation data points.
Precision Medicine Group is an organization that works in the medical field. They are an Equal Opportunity Employer, with employment decisions made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.
Identify and cultivate professional relationships with KOLs in designated tumor types.
Maintain cross-functional field partnerships allowing for appropriate collaboration with field commercial teams.
Develop scientific expertise on all Celcuity’s products, related disease states, and the clinical practice for a given therapeutic area.
Celcuity is a clinical-stage, publicly traded biotechnology company seeking to extend the lives of cancer patients through the development of targeted therapies for the treatment of multiple solid tumor indications. The company was founded to develop a better way to treat the cellular drivers of tumor growth.
Responsible for timely and quality delivery of site activation readiness, mitigating risks.
Prepare Clinical Trial Application Forms and submission dossiers for regulatory bodies.
Maintain project plans, trackers, and regulatory intelligence tools.
Precision for Medicine is a Clinical Research Organization with an integrated offering that combines clinical trial designs, operational and medical experts, and biomarker and data analytics solutions. They have a passion for rare diseases and oncology, and are growing their team.