Job Description EU Labeling Lead Associate Director Job Description General Summary The purpose of Global... required. Master’s degree preferred Extensive pharmaceutical or relevant experience with a focus on EU regulatory product labeling...
The Compliance Lead is a senior member of the Quality and Compliance Team responsible for monitoring and maintaining...) or medical signatory. Responsibilities: The Compliance Lead at PharmaReview is responsible for: Being a subject matter...
. OUR COMPANY Quell Therapeutics Ltd ("Quell"), the world leader in the development of engineered T-regulatory (Treg) cell... adherence to project contracts and assists in the identification and development of scope change documents. Lead or Support...
such as options analysis and exit strategy, digital portfolio dashboarding, liability assessments, asset recycling, regulatory... adaptation strategies, portfolio risk heat mapping for emerging risks such as PFAS, regulatory and stakeholder engagement...
, Submission, Project, Program, JCST, DEM, Biometrics, Clinical & Regulatory Solutions Team (CRST), Early Phase Perform relevant... experience in a clinical or pharmaceutical related field is required. Prior experience in a Data Management related field...
development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global... will be critical for this role. This professional will be expected to lead the programming and fine-tuning of various AI tools...
Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission... is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach...
development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global...Job Summary We are currently seeking an experienced data analyst to join our Informatics team who will lead advanced...
including the completion of gap analyses vs global document updates. Lead the completion of Product Quality Review...). Quality Management System Lead Auditor or Pharmaceutical GMP Lead Auditor Qualification Membership of an acceptable...
with biostatistics in ensuring that pharmaceutical drug-development plans are executed efficiently with timely and high-quality... deliverables in Novartis Global Drug Development. This role offers hybrid working, requiring 3 days per week in our London office...
partner, creating compelling submissions that meet rigorous regulatory standards. With a global footprint across four...MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, including clinical trial transparency...
position is a key collaborator and strategic partner with biostatistics in ensuring that pharmaceutical drug-development plans... in Novartis Global Drug Development are executed efficiently with timely and high-quality deliverables. This role offers hybrid...
submissions that meet rigorous regulatory standards. With a global footprint across four continents, MMS maintains a 97 percent... years of previous experience in the pharmaceutical industry Must have at least 3-5 years of industry regulatory writing...
partner, creating compelling submissions that meet rigorous regulatory standards. With a global footprint across four... protocol experience, as lead author, required Experience leading and managing teams while authoring regulatory documents...
teams (e.g., business development, external innovation, medical affairs, R&D, regulatory, finance, countries, global pricing.... Business Development & External Innovation: Commercial Evaluations Be the commercial lead across all stages of the business...
as the subject matter expert medical advisor and lead the development and implementation of the oncology medical plan in the... with market access, regulatory, and development teams to streamline patient access to our innovative therapies through health...
Global Medical Indication Lead During initial review of protocol, consults with internal groups and support staff regarding... a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the...
ATCs. Defines the on-boarding strategy and lead the co-ordination activation process for all ATCs in territory (starts pre... of progress made vs goals. Provides guidance to the ATCs to ensure patients can be treated (at regulatory approval) with our new...
as the subject matter expert medical advisor and lead the development and implementation of the oncology medical plan in the... closely with market access, regulatory, and development teams to streamline patient access to our innovative therapies through...
Responsibilities Strategic Output and Client Leadership Lead the strategic development for key healthcare and pharma clients.... Team Leadership and Development Lead training initiatives such as strategy inductions with new clients, health-focused...