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Editas MedicineCambridge
the power and potential of CRISPR/Cas9 and CRISPR/Cpf1 (Cas12a) gene editing.
We believe our people are at the core of everything we do, and we’re committed to cultivating a culture where every individual feels valued and included. To do this, we strive...
CD PROJEKT REDBoston, 4 mi from Cambridge
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OutlierBoston
In this role, you will become an AI Content Editor, assessing the quality of AI-generated writing, reviewing the work of fellow writers, and crafting original responses to prompts in order to teach the model what truly excellent writing looks like.
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OutlierBoston
In this role, you will become an AI Content Writer, assessing the quality of AI-generated writing, reviewing the work of fellow writers, and crafting original responses to prompts in order to teach the model what truly excellent writing looks like.
Highlights:</strong></p><ul><l...
OutlierBoston
In this role, you will become an AI Content Editor, assessing the quality of AI-generated writing, reviewing the work of fellow writers, and crafting original responses to prompts in order to teach the model what truly excellent writing looks like.
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Wilmington plcBoston, 4 mi from Cambridge
Company Outline
Job Role: Editor in Chief
Location: Hybrid - Boston, USA
Salary: Competitive (DoE)
Why do we want you?
For an experienced Editor in Chief/ Chief Editor/ Senior Editor, this is a rare and exciting opportunity to join a premier...
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Senior Director, Clinical Data Management
Editas Medicine | Cambridge | Full-time | apply.workable.com |
At Editas, we’re driven by a collective purpose, to bring transformative and life changing therapies to people living with serious diseases with the greatest unmet needs. This fuels our drive to excel in scientific innovation, allowing us to harness the power and potential of CRISPR/Cas9 and CRISPR/Cpf1 (Cas12a) gene editing.
We believe our people are at the core of everything we do, and we’re committed to cultivating a culture where every individual feels valued and included. To do this, we strive to integrate belonging, inclusivity, diversity, and equity into every aspect of our organization.
Together, we are leading the way towards a healthier and more equitable future.
Position Summary
Reporting to the VP of Biometrics, the Director/Sr. Director, Clinical Data Management is responsible for all clinical data management activities related to the effective planning and timely delivery of complete, high quality and reliable clinical trial data.
This person is expected to be a highly experienced functional area project and people leader with expert knowledge of Data Management strategy, operations and processes, and excellent people leadership skills.
Key Responsibilities:
• As the Director/Sr. Director, Clinical Data Management, you will be responsible for:
• Provide leadership and drive strategic direction of Data Management
• Provide guidance and mentorship to direct reports
• Develop DM standards and procedures
• Review/approve DM-related documents (e.g. eCRF and edit check requirements, Clinical Data Management Plan, CRF Completion Guidelines), as applicable
• Manage DM resources and contracts
• Drive the selection, collaborations and oversight of CROs and external vendors to ensure efficiency, quality, and consistency for all DM deliverables
• Develop and maintain expert competencies within Data Management
• Ensure compliance with regulatory and industry process and quality standards
• Represent DM in regulatory inspections
• Collaborate with cross-functional leads to ensure team effectiveness
Requirements
The ideal candidate will possess:
• Bachelor’s degree in the scientific/healthcare or related field; Master’s or Advanced degree preferred
• A minimum of 12 years (Director) to 15 years (Sr. Director) of professional DM experience in Pharmaceutical, Biotech, or CRO industry
• Experience in Rare Disease Drug Development and familiarity with gene and/or cell therapy preferred
• Significant end-to-end, hands-on experience in all aspects of data management
• Significant experience working with clinical trials
• Significant experience and extensive knowledge of the complex and interdependent relationships between protocol development, data collection, data review, and cleaning activities, analysis and reporting
• Significant experience leading data management activities for clinical trials; expert knowledge of DM processes, tools, methodologies and documentation; expert understanding of DM strategy
• Significant experience with EDC platforms and database design, including Medidata Rave and Oracle Clinical Inform
• Significant experience of clinical DM outsourcing with full service global CROs and niche providers
• Knowledge of GCP, FDA, ICH, CDISC, CDASH regulations and guidelines
• Experience in resource and budget management
• Experience in regulatory inspections
• Excellent verbal and written communication skills
Benefits
Benefits Summary:
Editas provides a comprehensive array of benefits to all employees, including a Blue Cross Blue Shield PPO Medical Plan, a company-funded Health Savings Account, Dental and Vision Insurance, Life and Disability Insurance, Dependent Care Account, Tuition Reimbursement, 401(k) plan with company match, Employee Stock Purchase Plan, Employee Assistance Plan, Wellness Programs, and a flexible Paid Time Off policy.
If you are a results-focused and collaborative professional with a passion for advancing transformative therapies, we invite you to apply. Join us at the forefront of genetic innovation and be a key contributor to Editas Medicine's mission of redefining healthcare through cutting-edge genetic technologies.
Fostering Belonging. Fueling Innovation. Transforming Lives.
We believe our people are at the core of everything we do, and we’re committed to cultivating a culture where every individual feels valued and included. To do this, we strive to integrate belonging, inclusivity, diversity, and equity into every aspect of our organization.
Together, we are leading the way towards a healthier and more equitable future.
Position Summary
Reporting to the VP of Biometrics, the Director/Sr. Director, Clinical Data Management is responsible for all clinical data management activities related to the effective planning and timely delivery of complete, high quality and reliable clinical trial data.
This person is expected to be a highly experienced functional area project and people leader with expert knowledge of Data Management strategy, operations and processes, and excellent people leadership skills.
Key Responsibilities:
• As the Director/Sr. Director, Clinical Data Management, you will be responsible for:
• Provide leadership and drive strategic direction of Data Management
• Provide guidance and mentorship to direct reports
• Develop DM standards and procedures
• Review/approve DM-related documents (e.g. eCRF and edit check requirements, Clinical Data Management Plan, CRF Completion Guidelines), as applicable
• Manage DM resources and contracts
• Drive the selection, collaborations and oversight of CROs and external vendors to ensure efficiency, quality, and consistency for all DM deliverables
• Develop and maintain expert competencies within Data Management
• Ensure compliance with regulatory and industry process and quality standards
• Represent DM in regulatory inspections
• Collaborate with cross-functional leads to ensure team effectiveness
Requirements
The ideal candidate will possess:
• Bachelor’s degree in the scientific/healthcare or related field; Master’s or Advanced degree preferred
• A minimum of 12 years (Director) to 15 years (Sr. Director) of professional DM experience in Pharmaceutical, Biotech, or CRO industry
• Experience in Rare Disease Drug Development and familiarity with gene and/or cell therapy preferred
• Significant end-to-end, hands-on experience in all aspects of data management
• Significant experience working with clinical trials
• Significant experience and extensive knowledge of the complex and interdependent relationships between protocol development, data collection, data review, and cleaning activities, analysis and reporting
• Significant experience leading data management activities for clinical trials; expert knowledge of DM processes, tools, methodologies and documentation; expert understanding of DM strategy
• Significant experience with EDC platforms and database design, including Medidata Rave and Oracle Clinical Inform
• Significant experience of clinical DM outsourcing with full service global CROs and niche providers
• Knowledge of GCP, FDA, ICH, CDISC, CDASH regulations and guidelines
• Experience in resource and budget management
• Experience in regulatory inspections
• Excellent verbal and written communication skills
Benefits
Benefits Summary:
Editas provides a comprehensive array of benefits to all employees, including a Blue Cross Blue Shield PPO Medical Plan, a company-funded Health Savings Account, Dental and Vision Insurance, Life and Disability Insurance, Dependent Care Account, Tuition Reimbursement, 401(k) plan with company match, Employee Stock Purchase Plan, Employee Assistance Plan, Wellness Programs, and a flexible Paid Time Off policy.
If you are a results-focused and collaborative professional with a passion for advancing transformative therapies, we invite you to apply. Join us at the forefront of genetic innovation and be a key contributor to Editas Medicine's mission of redefining healthcare through cutting-edge genetic technologies.
Fostering Belonging. Fueling Innovation. Transforming Lives.
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