Medical Director, Clinical Development
Position Overview:
The Medical Director in Clinical Development will serve as the Medical Lead for base editing gene therapies in hematology.
The Medical Director will work with cross-functional multidisciplinary study teams on clinical development strategy, clinical trial design and execution including medical monitoring of assigned trials, and support in-scope aspects of global regulatory interactions.
Though this is a hybrid role, candidates must live local and be able to visit our Cambridge location 1-3 days per week as needed.
Responsibilities:
Serves on cross-functional teams for assigned programs, working with other team members to drive program and clinical strategy to registration in applicable populations and indicationsSupport development of Target Product Profile (TPP) and Clinical Development Plan (CDP)Serves as the medical monitor for assigned studies (focus will be in hematology programs) including design, execution and interpretation of study data.
Provides scientific and clinical input to study-related documents and analysis plans including Informed consent forms (ICF), clinical research forms (CRF), statistical analysis plans (SAP), clinical pharmacology and biomarker analysis plans.
Ensure patient safety on clinical trials and adherence to Good Clinical Practices (GCP).
Contribute to the development of regulatory documents in support of regulatory submissions, including clinical section of IND's and CTA's, safety reports, responses to regulatory authorities and Ethics Committees/IRBs, and other documents as appropriate.
Acts as liaison between Clinical Development and other internal groups at BEAM for assigned studies, including working closely with clinical operations, pharmacovigilance, manufacturing, quality and biomarker groups to facilitate and coordinate cross-functional study activities.
Establishes strong collaborations with study investigators, outside medical experts and represents BEAM during investigator meetings and advisory boards.
Contribute to the development and planning of Advisory Board meetings in the relevant therapeutic areas
Qualifications:
MD, DO or equivalent ex-US medical degree with 12
years experience, 3
years clinical trial experience in industry is a must.
Board certification/eligibility in hematology/oncology, or another relevant specialty highly desired.
Must have previous patient care experience.
Pharmaceutical/Biotech industry experience in clinical development and medical monitoringStrong oral and written communication skills to influence othersAbility to work collaboratively in a fast-paced, team-based matrix environment and to function independently as appropriateClinical development and/or clinical experience in rare disease, cell & gene therapy is a plusAbility to work independently to resolve challenges.
Estimated Salary: $20 to $28 per hour based on qualifications.
The Medical Director in Clinical Development will serve as the Medical Lead for base editing gene therapies in hematology.
The Medical Director will work with cross-functional multidisciplinary study teams on clinical development strategy, clinical trial design and execution including medical monitoring of assigned trials, and support in-scope aspects of global regulatory interactions.
Though this is a hybrid role, candidates must live local and be able to visit our Cambridge location 1-3 days per week as needed.
Responsibilities:
Serves on cross-functional teams for assigned programs, working with other team members to drive program and clinical strategy to registration in applicable populations and indicationsSupport development of Target Product Profile (TPP) and Clinical Development Plan (CDP)Serves as the medical monitor for assigned studies (focus will be in hematology programs) including design, execution and interpretation of study data.
Provides scientific and clinical input to study-related documents and analysis plans including Informed consent forms (ICF), clinical research forms (CRF), statistical analysis plans (SAP), clinical pharmacology and biomarker analysis plans.
Ensure patient safety on clinical trials and adherence to Good Clinical Practices (GCP).
Contribute to the development of regulatory documents in support of regulatory submissions, including clinical section of IND's and CTA's, safety reports, responses to regulatory authorities and Ethics Committees/IRBs, and other documents as appropriate.
Acts as liaison between Clinical Development and other internal groups at BEAM for assigned studies, including working closely with clinical operations, pharmacovigilance, manufacturing, quality and biomarker groups to facilitate and coordinate cross-functional study activities.
Establishes strong collaborations with study investigators, outside medical experts and represents BEAM during investigator meetings and advisory boards.
Contribute to the development and planning of Advisory Board meetings in the relevant therapeutic areas
Qualifications:
MD, DO or equivalent ex-US medical degree with 12
years experience, 3
years clinical trial experience in industry is a must.
Board certification/eligibility in hematology/oncology, or another relevant specialty highly desired.
Must have previous patient care experience.
Pharmaceutical/Biotech industry experience in clinical development and medical monitoringStrong oral and written communication skills to influence othersAbility to work collaboratively in a fast-paced, team-based matrix environment and to function independently as appropriateClinical development and/or clinical experience in rare disease, cell & gene therapy is a plusAbility to work independently to resolve challenges.
Estimated Salary: $20 to $28 per hour based on qualifications.
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