Remote Jobs at Acadia Pharmaceuticals

- Completed training as Industrieelektroniker (m/w/d) specializing in Automation - Completed training as Industrieelektroniker (m/w/d) specializing in Devices & Systems - Completed training as Mechatroniker (m/w/d) - Completed training as Industriemechaniker (m/w/d) - Ideally, additional qualification as "Elektrofachkraft" - Good understanding of process flows, e.g., maintaining process technology of installed production plants, ensuring high technical plant availability, and maintaining operati…

- Details not provided in the original job description

Candidates should possess an apprenticeship as a pharmacist (Pharmacie), chemist (Chemie), or a comparable vocational training in a technical field such as chemistry, biology, pharmacy, medicine, or food technology. Prior experience in the manufacture of sterile pharmaceuticals is desirable. Applicants should have an understanding of GMP-compliant documentation and behavior in cleanrooms, as well as good knowledge of MS Office programs, especially Excel and Outlook.

- Pharmakant (m/w/d) - At least a good mittlerer Schulabschluss (MSA) - Interest in physical, chemical, mathematical, and technological connections - Interest in pharmaceutical manufacturing processes - Quick perception, enthusiasm for new things, good observation skills - Works well in a team with a careful and responsible work ethic - Good German skills in spoken and written form - Chemielaborant (m/w/d) - Interest in physical, chemical, mathematical, natural science, technical connections, an…

- BA/BS degree in a scientific discipline; advanced scientific degree preferred - Minimum 7+ years of Pharmaceutical/Biotech industry experience in drug advertising and promotion review - 4+ years’ experience as the primary Regulatory representative in the review of prescription drug advertising and promotion for compliance with applicable FDA laws, regulations, and guidance documents, including direct experience communicating with OPDP - Significant Subpart H and/or Subpart E submission experie…

- Navigate the intricacy of urologic & uro-oncologic settings of care - Cover North and South Carolina geographical area - Engage with urologists, oncologists, nurses, pharmacists, administrators, teaching institutions, and formulary committees - Participate in company-sponsored and/or company-approved training programs - Maintain knowledge of product (clinical acumen)

The Executive Director, Commercial Data Strategy and Analytics should have a strong track record in building and scaling global commercial data ecosystems. Experience in the biopharmaceutical industry, specifically with NASH therapeutics like Rezdiffra, is essential. The role requires oversight of commercial analytics and data management teams, with a need for cross-functional insight generation across U.S. and ex-U.S. markets. Expertise in integrating specialty pharmacy, hub, claims, CRM, payer…

- MR certification - Driver's license - Willingness to transfer nationwide - 5+ years of MR experience at a pharmaceutical company - Experience handling university hospitals and major large-scale hospitals - PC skills - (Preferred) Experience in oncology - (Preferred) Experience in urology - (Preferred) Pharmacist qualification

- MR certification (MR認定証) - Driver's license (運転免許証) - Willingness to transfer nationwide (全国転勤可能な方) - 5+ years of MR experience at a pharmaceutical company (製薬企業にて5年以上のMR経験) - Experience handling university hospitals and major large-scale hospitals (大学病院および主要な大規模病院の担当経験) - PC skills (PCスキル) - Preferred (歓迎要件) - Experience in oncology (がん領域の経験) - Experience in urology (泌尿器領域の経験) - Pharmacist qualification (薬剤師資格)

- Bachelor’s degree in life sciences - Minimum of 3 years direct pharmaceutical industry experience dealing with global clinical study individual case safety report processing and reporting preferred; post-approval safety experience highly desired - Detailed knowledge of relevant US, EU, and ICH guidelines, initiatives and regulations governing both clinical studies and post-approval safety - Safety database experience is required (e.g., Argus) - Proficient in MS Word, Excel, PowerPoint, Outlook…

- Bachelor’s degree or above in Medical, Pharmacy or related areas - At least 5 years related product & marketing experience in pharmaceutical industry - Fluency in both written and oral English - Good product analysis and project management skills - Positive work attitude and good communication skills

- Bachelor’s or Master’s degree in biological or life sciences or related scientific discipline, pharmacy or medicine (or international equivalent); an advanced degree is desirable - A minimum of 15 years in the pharmaceutical industry with a minimum of 12 years in Global Regulatory Affairs - Experience with major Health Authorities (US FDA, Health Canada, and EMA) is mandatory - Strong understanding of US FDA, EU and international pharmaceutical guidance, regulations, drug development process, …

- Advanced healthcare or life science degree (e.g., PA, NP, PharmD, or other clinically relevant background) - Minimum 5 years of direct patient care in gastroenterology, hepatology, endocrinology, or metabolic disease - Clinical familiarity with NASH/MASH diagnostic tools, especially non-invasive testing and risk stratification methods - Strong grasp of U.S. healthcare system operations, including practice workflows, billing/coding, and payer dynamics - Excellent verbal and written communicatio…

Candidates should possess an advanced degree in a scientific or healthcare field and have over 10 years of experience in clinical research and organizational management within the pharmaceutical industry, with a preference for biotech or small pharma experience. Experience with global clinical trials is also required.

- 医学、药学、护理、医药市场营销等相关专业本科或以上学历。 - 至少2年以上医药销售经验。 - 外企背景，生殖领域经验优先。 - 倾向男生。 - 学习能力及学术性强。 - 善于大客户管理。 - 以客户为中心。 - 行动导向、毅力、计划性。 - 专业技能学习能力强。 - 追求成效，具备道德与价值观。