Medical Director/Scientific Director, Medical Affairs
6 hours ago
AbbVie is seeking an exceptional Medical Director/Scientific Director, Medical Affairs to provide expertise in the prevention and management of corneal events associated with targeted cancer therapies.
Key Responsibilities:- Develop and execute a comprehensive medical strategy for the management of ocular events related to targeted cancer therapies.
- Stay up-to-date with professional information and technology through conferences and medical literature.
- Represent Ocular Medical Affairs in designated cross-functional Oncology teams across the organization.
- Manage expert optometric and ophthalmic KOL relationships.
- Execute on key medical functional deliverables aligned to ocular medical strategy.
- Doctor of Optometry (O.D.), Medical Doctorate (M.D.) degree or equivalent with expertise in the ocular anterior segment.
- Minimum of 2 years of medical affairs experience in the pharmaceutical industry or equivalent.
- Solid understanding of the eye care clinical landscape and collaborative care practice patterns between eye care professionals and other healthcare providers.
- Knowledge of clinical trial methodology, data analysis and interpretation, and regulatory requirements governing clinical trials.
- A comprehensive package of benefits including paid time off, medical/dental/vision insurance, and 401(k) to eligible employees.
- Opportunities for professional growth and development.
- A collaborative and dynamic work environment.
AbbVie is a global biopharmaceutical company that discovers and delivers innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow.
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Associate Director of Medical Affairs
2 weeks ago
Waltham, Massachusetts, United States Apellis Full timeJob OpportunityWe are seeking a highly skilled Associate Director of Medical Affairs to join our team at Apellis Pharmaceuticals, Inc. This is a key role that will play a critical part in implementing our global medical affairs strategy and driving execution across medical affairs activities.Key ResponsibilitiesSupport the implementation of our global...
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Regulatory Affairs Director
2 weeks ago
Waltham, Massachusetts, United States Taylor Strategy Partners Full timeJob Title: Director, Regulatory Affairs Job Summary: We are seeking a highly experienced Director, Regulatory Affairs to lead our regulatory strategy and operations. As a key member of our team, you will be responsible for developing and implementing a consolidated regulatory strategy to secure and maintain market access for our products. Key...
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Regulatory Affairs Director
3 weeks ago
Waltham, Massachusetts, United States Weber & Company Full timeExecutive Director Regulatory AffairsJob Summary:Weber & Company is seeking an experienced Executive Director Regulatory Affairs to lead our client's regulatory affairs team in Greater Boston. As a key member of the leadership team, you will be responsible for developing and implementing a regulatory strategy that accelerates product approvals and maintains...
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Waltham, Massachusetts, United States Upstream Bio Full timeJob Title: Medical Director/Senior Medical Director of Clinical DevelopmentWe are seeking a highly motivated and experienced Medical Director/Senior Medical Director of Clinical Development to lead clinical program(s) for verekitug in COPD. This role will report to the Vice President, Clinical Development.The successful candidate will be a leader in the...
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Waltham, Massachusetts, United States Upstream Bio Full timeJob Title: Medical Director/Senior Medical Director of Clinical DevelopmentWe are seeking a highly motivated and experienced Medical Director/Senior Medical Director of Clinical Development to lead clinical program(s) for verekitug in COPD. This role will report to the Vice President, Clinical Development.The successful candidate will be a leader in the...
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Associate Director, Regulatory Affairs
4 days ago
Waltham, Massachusetts, United States Alkermes Full timeJob DescriptionOverview:At Alkermes, we are committed to developing medicines that address unmet patient needs. As an Associate Director of CMC Regulatory Affairs, you will play a critical role in supporting post-approval CMC changes and global Supply Chain and GMP activities for our marketed products.Key Responsibilities:Develop and lead regulatory CMC...
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Regulatory Affairs Director
4 weeks ago
Waltham, Massachusetts, United States Trebla Talent Full timeJob Title: Executive Director, Regulatory AffairsCompany: Trebla TalentLocation: Massachusetts - HybridJob Type: Full-timeAbout the Company:Trebla Talent is a leading recruitment agency specializing in placing top talent in the biotech and pharmaceutical industries.Job Description:We are seeking an experienced Executive Director to lead our Regulatory...
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Regulatory Affairs Director
2 weeks ago
Waltham, Massachusetts, United States Dyne Therapeutics Full timeJob Title: Associate Director, Regulatory CMCThe Associate Director, Regulatory Chemistry Manufacturing and Control (CMC) plays a pivotal role in executing global CMC regulatory strategies for our programs in early and late-stage development through and beyond approval. This position supports Dyne's clinical registration, commercial development, and...
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Waltham, Massachusetts, United States Upstream Bio Full timeJob SummaryWe are seeking a highly experienced Medical Director/Senior Medical Director of Clinical Development to lead clinical programs for verekitug in COPD. This role will report to the Vice President, Clinical Development.Key ResponsibilitiesDevelop and execute clinical development plans and study protocols in collaboration with cross-functional...
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Waltham, Massachusetts, United States Upstream Bio Full timeJob SummaryWe are seeking a highly experienced Medical Director/Senior Medical Director of Clinical Development to lead clinical programs for verekitug in COPD. As a key member of our team, you will be responsible for guiding the development of clinical strategies, prioritizing study protocols, and ensuring scientific integrity in the execution of clinical...
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Regulatory Affairs Director
4 weeks ago
Waltham, Massachusetts, United States Trebla Talent Full timeRole:We are seeking a seasoned Regulatory Affairs expert to lead our team and drive strategic decisions across our portfolio.Company Overview:Trebla Talent is proud to partner with a pre-IPO, clinical-stage biotech company that is revolutionizing cancer and autoimmune treatments through innovative immunotherapies.Key Responsibilities:As the Executive...
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Chief of Staff
3 weeks ago
Waltham, Massachusetts, United States Apellis Full timeJob SummaryApellis Pharmaceuticals, Inc. is seeking a highly skilled and experienced Chief of Staff to support the Chief Medical Officer (CMO) in driving the company's medical affairs strategy and operations. The ideal candidate will have a strong background in medical affairs, excellent communication and leadership skills, and the ability to work...
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Regulatory Affairs Director
2 weeks ago
Waltham, Massachusetts, United States Dyne Therapeutics Full timeJob Title: Associate Director, Regulatory CMCThe Associate Director, Regulatory Chemistry Manufacturing and Control (CMC) is a critical role at Dyne Therapeutics, responsible for executing global CMC regulatory strategies for our programs in early and late-stage development through and beyond approval.Key Responsibilities:Lead CMC regulatory execution for...
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Regulatory Affairs Director
3 weeks ago
Waltham, Massachusetts, United States Dyne Therapeutics Full timeJob Title: Associate Director, Regulatory CMCThe Associate Director, Regulatory Chemistry Manufacturing and Control (CMC) plays a pivotal role in executing global CMC regulatory strategies for our programs in early and late-stage development through and beyond approval. This position supports Dyne's clinical registration, commercial development, and...
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Medical Director, Pharmacovigilance Expert
4 weeks ago
Waltham, Massachusetts, United States Deciphera Pharmaceuticals Full timeJob Title: Medical Director, PharmacovigilanceDeciphera Pharmaceuticals is seeking a highly skilled Medical Director to lead our Pharmacovigilance team. As a key member of our organization, you will be responsible for ensuring the safety of our products and managing risk across the globe.Key Responsibilities:Lead global pharmacovigilance activities for...
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Regulatory Affairs Director
6 days ago
Waltham, Massachusetts, United States Innoviva Specialty Therapeutics Full timeJob Title: Vice President, Head of Regulatory AffairsAt Innoviva Specialty Therapeutics, we are seeking a highly experienced and skilled Vice President, Head of Regulatory Affairs to lead our regulatory strategy and ensure compliance with global regulatory requirements.Job Summary:The successful candidate will be responsible for developing and executing...
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Medical Director, Pharmacovigilance Expert
3 weeks ago
Waltham, Massachusetts, United States Deciphera Pharmaceuticals Full timeJob Title: Medical Director, PharmacovigilanceDeciphera Pharmaceuticals is seeking a highly skilled Medical Director to lead our Pharmacovigilance team. As a key member of our organization, you will be responsible for ensuring the safety of our products and providing medical expertise to support our global operations.Key Responsibilities:Lead and provide...
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Medical Director of Clinical Development
4 weeks ago
Waltham, Massachusetts, United States Upstream Bio Full timeJob SummaryWe are seeking a highly experienced Medical Director/Senior Medical Director of Clinical Development to lead clinical programs for our innovative therapeutics, verekitug, in COPD. As a key member of our clinical development team, you will be responsible for guiding the development of clinical strategies, prioritizing study protocols, and ensuring...
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Regulatory Affairs Director
4 weeks ago
Waltham, Massachusetts, United States Dyne Therapeutics Full timeJob SummaryThe Associate Director, Regulatory Affairs CMC is a critical role at Dyne Therapeutics, responsible for executing global CMC regulatory strategies for our programs in early and late-stage development through and beyond approval.Key ResponsibilitiesLead CMC regulatory execution for specific programs at all stages of developmentProvide strategic...
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Associate Director Regulatory Affairs CMC
8 hours ago
Waltham, Massachusetts, United States Dyne Therapeutics Inc Full timeJob Title: Associate Director, Regulatory Affairs CMCDyne Therapeutics Inc is seeking an experienced Associate Director, Regulatory Affairs CMC to join our team. As a key member of our Regulatory Affairs department, you will be responsible for executing global CMC regulatory strategies for our programs in early and late-stage development through and beyond...