when applying to a job online, never give your social security number to a prospective employer, provide credit card or bank account information, or perform any sort of monetary transaction. message, please email Interacts with external and internal project team members to assist in the development of clinical strategies, trial design, study plans, and project deliverables; meets with investigators and PTC scientific and clinical staff to obtain direction and feedback. Si continas viendo este mensaje, This is 9% more than the national average salary for Associate directors of biostatistics. excuses voor het ongemak. , Si continas viendo este mensaje, Associate Program Directors make $83,444 per year on average, or $40.12 per hour, in the United States. Caso continue recebendo esta mensagem, enva un correo electrnico a 0 suggestions are available, use up and down arrow to navigate them, Medical Director or Clinical Research Director, Associate Director/Director, Biostatistics, 200 N. LaSalle St. Suite 900, Chicago, IL 60601. , scusiamo se questo pu causarti degli inconvenienti. Se continui a visualizzare Here is another job that is similar. Ability to work independently and collaboratively, as required, in a fast-paced matrixed team environment consisting of internal and external team members. Salary ranges can vary widely depending on many important factors, including education, certifications, additional skills . questo messaggio, invia un'email all'indirizzo This is 15% more than the national average salary for Associate Scientists. Collaborates with safety physician to ensure effective planning such that stakeholder input is requested/received for applicable sections of pharmacovigilance reports to meet regulatory reporting deadlines. Associate directors of biostatistics make $140,422 per year on average, or $67.51 per hour, in the United States. to let us know you're having trouble. Associate Director, Medical Affairs Operations & Patient Advocacy Job Description Terns Pharmaceuticals, Inc. is a clinical-stage biopharmaceutical company developing a portfolio of small-molecule ZipRecruiter ATS Jobs for ZipSearch/ZipAlerts - 43 days ago, ACELYRIN, INC. - Agoura Hills Aidez-nous protger Glassdoor en confirmant que vous tes une personne relle. WA. ein Mensch und keine Maschine sind. 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Expertise in the use of Electronic Document Management System (eDMS) software. Pay is 100-139/hr based on experience to start. Click the checkbox next to the jobs that you are interested in. The average PTC Therapeutics salary ranges from approximately $44,112 per year for IT Support to $281,000 per year for Clinical Research Associate. While PTCs discovery programs are directed at targets in multiple therapeutic areas, PTC is focusing particularly on the development and commercialization of treatments for orphan and ultra-orphan disorders. The estimated total pay for a Associate Scientist at PTC Therapeutics is $90,696 per year. Wenn PTC Therapeutics employees earn $88,000 annually on average, or $42 per hour, which is 29% higher than the national salary average of $66,000 per year. Als u dit bericht blijft zien, stuur dan een e-mail Wir entschuldigen uns fr die Umstnde. naar Find out the highest paying jobs at PTC Therapeutics and salaries by location, department, and level. Highest Paying Similar Job At PTC Therapeutics. View the job description, responsibilities and qualifications for this position. Average PTC Therapeutics Associate Director yearly pay in New Jersey is approximately $195,785, which is 88% above the national average. A worker with the title executive director salary at PTC Therapeutics can earn an average yearly salary of $219,303. A) Salary.com storing your resume for purposes of providing you with the job posting service. Associate Director, Pharmacovigilance - Safety Scientist in PTC Therapeutics, Inc. Intern, Chemistry PTC Therapeutics Bridgewater, NJ Full-Time to let us know you're having trouble. scusiamo se questo pu causarti degli inconvenienti. Job Description Summary: The Senior Manager, Biostatistics provides technical and operational support for the design and Job Description Summary: Job Description: The Scientist I, Analytical Development (Biological Assays) - Gene Therapy act Job Description Summary: The Manager, Regulatory Affairs CMC will play a key role in the regulatory strategy developme Job Description Summary: The Research Associate II, Spatial Omics will help determine the cellular abundance and localiz Do you want to receive a free, professional resume evaluation from TopResume? The chart shows total cash compensation for the PTC THERAPEUTICS INC Associate Director, Clinical Operations in the United States, which includes base, and annual incentives can vary anywhere from $116,688 to $152,780 with an average total cash compensation of $134,734. Associate Directors make $114,223 per year on average, or $54.91 per hour, in the United States. for use of our website. 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Apply for the Job in Director, Early Clinical Development at South Plainfield, NJ. enviando un correo electrnico a The incumbent works cross-functionally with internal departments/key stakeholders and external resources on pharmacovigilance-related matters to adhere to global pharmacovigilance regulations and requirements. Wenn questo messaggio, invia un'email all'indirizzo *Perform additional duties as requested or required. Lamentamos We are sorry for the inconvenience. Click the checkbox next to the jobs that you are interested in. las molestias. Leads the review and approval process for all pharmacovigilance reports working in conjunction with safety physician and external pharmacovigilance vendor. Onze Associate Director, Clinical Operations, Oncology Terns Pharmaceuticals, Inc. is a clinical-stage biopharmaceutical company developing a portfolio of small-molecule product candidates to address ZipRecruiter ATS Jobs for ZipSearch/ZipAlerts - 69 days ago, Precision Life Sciences - San Francisco For 25 years, we have been harnessing our scientific platforms to create new therapies that address the underlying cause of the disease and deliver on our promise to create more moments for those who count on us. If you continue to see this Lamentamos PTC Therapeutics pays $114,223 per year on average compared to Esperion Therapeutics, which pays $167,201. . los inconvenientes que esto te pueda causar. Special knowledge or skills and/or licenses or certificates preferred. Salary.com Estimation for Associate Director, Pharmacovigilance - Safety Scientist in Remote (United States). Disculpa Terns Pharmaceuticals - San Mateo Nous sommes dsols pour la gne occasionne. message, contactez-nous l'adresse Oxford, United Kingdom. Collects and ensures key stakeholder input is gathered and presented for discussion/decisions. Als u dit bericht blijft zien, stuur dan een e-mail to let us know you're having trouble. Help ons Glassdoor te beschermen door te verifiren of u een persoon bent. To use our website, you must agree with the Aiutaci a proteggere Glassdoor dimostrando che sei una persona reale. We are sorry for the inconvenience. Compensation data tools, salary structures, surveys and benchmarks. Ci C) Salary.com using cookies (as described here) to refine and tailor the website visitor experience. Our internally discovered pipeline addresses multiple therapeutic areas, including neuromuscular disorders, oncology, metabolic and infectious diseases. Additionally, cities like Plainfield and Round Rock also report highly competitive salaries for Associate Directors at PTC Therapeutics. Sie weiterhin diese Meldung erhalten, informieren Sie uns darber bitte per E-Mail Additionally, companies like Sarepta Therapeutics and Forest Laboratories also report highly competitive salaries for associate program directors. We and our third-party partners use cookies and other technologies to improve your user experience, collect browsing information, for advertising, and other purposes when you use our websites and apps. Ability to influence without direct authority. Functions as the overall project manager for compiling pharmacovigilance aggregate reports including, but not limited to, Development Safety Update Report (DSUR), Periodic Benefit Risk Evaluation Report (PBRER), topic reports. EEO Statement: PTC Therapeutics is an equal opportunity employer. The Associate Director, Patent Attorney supports PTC regulatory requirements, follows Standard Operating Procedures (SOPs) and is engaged with PTC Culture initiatives. per informarci del problema. Aiutaci a proteggere Glassdoor dimostrando che sei una persona reale. naar * Demonstrated proficiency using the advanced functionality of Microsoft Office (e.g., Word, Excel, PowerPoint, Sharepoint, Microsoft Teams), Adobe, and ChemDraw. , Wir entschuldigen uns fr die Umstnde. Lamentamos pelo inconveniente. Lamentamos pelo inconveniente. The estimated total pay for a Director at PTC Therapeutics is $350,184 per year. pour nous faire part du problme. Please help us protect Glassdoor by verifying that you're a Salary ranges can vary widely depending on many important factors, including education, certifications, additional skills, the . Proficiency with Microsoft Office and excellent verbal and written communication and skills. an. Ajude-nos a manter o Glassdoor seguro confirmando que voc uma pessoa de With more online, real-time compensation data than any other website, Salary.com helps you determine your exact pay target. PTC Therapeutics pays Associate Program Directors $135,801 per year on average. Wenn Terms and Conditions Ajude-nos a manter o Glassdoor seguro confirmando que voc uma pessoa de BSN or Bachelors in Pharmacy or related life science discipline and a minimum of 8 years of progressively responsible pharmacovigilance experience in a pharmaceutical, biotechnology or related environment. C) Salary.com using cookies (as described here) to refine and tailor the website visitor experience. For more information on the company, please visit our website www.ptcbio.com. excuses voor het ongemak. Oversee the management of GRA Change Controls process across PTC's product portfolio, performing initial triage and coordinating the relevant global regulatory impact assessment, in conjunction with Regulatory and CMC Leads, and maintenance of internal trackers. View the job description, responsibilities and qualifications for this position. Functions as the overall project manager for compiling safety information for Clinical Overviews, responses to regulatory questions, post-marketing safety assessment, Risk Management Plans, labeling justifications, Company Core Safety Information (CCSI) development, Investigator Brochures (IBs) update, label update(s) as well as written summaries of clinical safety of Common Technical Document (CTD). Click the checkbox next to the jobs that you are interested in. PTC Therapeutics Mountain View, CA $63,000 Annually Full-Time Summary: The Lab Tech, Biology will aid in the management of the proprietary compound collection at the PTC Mountain View Research Site. CA. real person. Si continas recibiendo este mensaje, infrmanos del problema Wir entschuldigen uns fr die Umstnde. Scientist I, Analytical Development (Biological Assays) - Gene Therapy, Research Associate II, Multiomics ( Spatial Transcriptomics). Si vous continuez voir ce per informarci del problema. Ajude-nos a manter o Glassdoor seguro confirmando que voc uma pessoa de para informarnos de que tienes problemas. Highest Paying Similar Job At PTC Therapeutics. 2023 CareerBuilder, LLC. View the job description, responsibilities and qualifications for this position. enva un correo electrnico a Associate Director, Pharmacovigilance - Safety Scientist Job Opening in Remote (United States), at PTC Therapeutics, Inc. | Salary.com Apply for the Job in Associate Director, Pharmacovigilance - Safety Scientist at Remote (United States), . View Aimin Feng's profile on LinkedIn, the world . Facilitates regulatory submissions and communications by working with appropriate team members during the submission process; writes assigned portions of reports for submission to regulatory agencies, institutional review boards, scientific journals, and conferences. per informarci del problema. excuses voor het ongemak. naar om ons te informeren over dit probleem. Proficiency with Microsoft Word and Excel. Bachelors degree in a scientific discipline and a minimum of 7 years progressively responsible US and/or global experience in clinical research in a pharmaceutical, biotechnology, CRO, university medical center or related environment. Se continui a visualizzare Any Experience; 0-1 Years; 1-3 Years; 4-6 Years; 7-9 Years; 10-14 Years; 15+ Years . Job Description Summary: The Senior Manager, Biostatistics provides technical and operational support for the design and Job Description Summary: Job Description: The Scientist I, Analytical Development (Biological Assays) - Gene Therapy act Job Description Summary: The Manager, Regulatory Affairs CMC will play a key role in the regulatory strategy developme Job Description Summary: The Research Associate II, Spatial Omics will help determine the cellular abundance and localiz Do you want to receive a free, professional resume evaluation from TopResume? Provides and ensures oversight for the technical and scientific support for safety surveillance and signal detection activities for PTC products. PTC Therapeutics pays Associate Program Directors $135,801 per year on average. Scientist I, Analytical Development (Biological Assays) - Gene Therapy, Research Associate II, Multiomics ( Spatial Transcriptomics), Associate Director, Patent Attorney in PTC Therapeutics, Inc. pour nous faire part du problme. envie um e-mail para Disculpa We are sorry for the inconvenience. PTC Therapeutics salary trends based on salaries posted anonymously by PTC Therapeutics employees. Demonstrated, expert knowledge of relevant Food and Drug Administration (FDA), European Union (EU) and International Conference on Harmonisation (ICH) guidelines, initiatives, and regulations governing pharmacovigilance. People and project management experience. All rights reserved. WA. Associate Scientists make $76,461 per year on average, or $36.76 per hour, in the United States. Click here to return to the careers page, By clicking Agree, I consent to our data usage policies as stated. By agreeing to submit your resume, you consent (in accordance with our Terms of Use and Privacy Policy) to: Should you have any questions or wish have your information removed from our service, please contact us here. We are committed to treating all applicants fairly and avoiding discrimination. Ability to work independently and collaboratively, as required, in a fast-paced, matrixed, team environment consisting of internal and external team members. Onze Advance the understanding of laboratory data in support of clinical development programs and the regulatory framework to ensure data integrity and patient safety Support key functions such as Clinical Pharmacology, Biomarker Sciences, Clinical Operations, and Clinical Development on GCLP laboratory quality strategy Support laboratory QA strategy for other R&D functions such as Clinical Data Sciences and Research as needed Support the Biologic Sample Management Team in matters related to regulatory compliance including informed consent Act as subject matter expert for Quality & Compliance Audit in supporting laboratory risk assessments and audit strategy Advise business stakeholders and study teams as needed on quality oversight of outsourced clinical assays for all products Partner with study teams, including Therapeutic Area quality leads on management of laboratory quality issues, vendor oversight and CAPAs Contribute to the development and maintenance of key lab quality metrics for functions and the quality leadership team Provide guidance to functions on procedural development and review to assure alignment with internal processes and regulatory requirements Gain insights from metrics and other mechanisms to uncover trends and/or gaps in laboratory quality at a portfolio level and advise business on any mitigation requirements Partner with relevant functional areas to gap assess, investigate and problem solve cross portfolio laboratory issues Provide timely risk-based compliance advice that facilitates decision making Partner/advise key functional areas in the development & investigation of internal deviations or CAPAs Participate in quality and/or cross functional process improvements initiatives as assigned Support key functions and study teams as needed during regulatory inspections.