Gene Therapy
We are looking for experts in "gene therapies" to provide commentary and insights towards a startup developing a cell therapy that turns a patient’s own cells into miniature drug factories. We are an angel investing platform dedicated to connecting deep-tech startups with angel investors. By deep-tech we mean startups founded on scientific breakthroughs and technological innovations that create lasting impact on mankind.
as a participating expert* in this process, your involvement is limited to answering anywhere between 8-12 investor-submitted questions. This takes about 1 hour (+/-) . Once you are vetted, we send those questions via a web form for your responses. If your contribution is published, it will be viewable by potential investors in this startup, giving you an opportunity to make connections, socialize virtually, and gain bragging rights in a vibrant entrepreneurial and angel investing community.
*at this point, we cannot guarantee any monetary reimbursement. You do get insights to new upcoming technologies in your field and a tremendous networking opportunity!
+31 Other ResponsesGene Therapy
We are looking for experts in "gene therapy" to provide commentary and insights towards a startup that is developing a new approach for cell engineering using a proprietary silicon chip technology that delivers molecules into potentially, millions of individual cells.
We are an angel investing platform dedicated to connecting deep-tech startups with angel investors. By deep-tech we mean startups founded on scientific breakthroughs and technological innovations that create lasting impact on mankind.
As a participating expert* in this process, your involvement is limited to answering anywhere between 8-12 investor-submitted questions. This takes about 1 hour (+/-) . Once you are vetted, we send those questions via a web form for your responses. If your contribution is published, it will be view-able by potential investors in this startup, giving you an opportunity to make connections, socialize virtually, and gain bragging rights in a vibrant entrepreneurial and angel investing community.
*at this point, we cannot guarantee any monetary reimbursement. You do get insights to new upcoming technologies in your field and a tremendous networking opportunity!
+10 Other ResponsesClinical And Regulatory Medical Writing
This is a full-time employment opportunity onsite in southborough, ma.
**as a manager, clinical and regulatory medical writing you will:
- implement project-specific strategies and assist with the development and implementation of department strategies to increase productivity and quality.
- assist with the oversight of medical writing personnel. This includes hiring personnel, managing personnel matters, conducting performance evaluations, and training medical writing staff regarding applicable regulatory guidelines and medical writing practices.
- assist with resource allocation and the development of business proposals related to the medical writing functions.
- be responsible for the smooth functioning of all medical writing projects for clients and project teams through management of internal staff and the medical writing process.
- serve as the lead medical writer on projects when appropriate. As the lead medical writer, you will draft and finalize documents necessary for all phases of clinical drug and device development, work with project managers to develop timelines and resource plans for the production of clinical documents, review statistical analysis plans and crfs, and perform peer and qc review of clinical study reports and clinical sections of regulatory submissions written by other medical writers.
- and more!
**required education and experience**:
- bachelor’s degree or advanced degree, with some applied training relevant to the clinical trials or health research environment.
- at least 5 years of medical writing experience in a cro, pharmaceutical, or biotechnology setting. Management experience preferred.
- thorough knowledge of ich gcp guidelines and other applicable regulatory rules and guidelines and of medical terminology, clinical trials, and clinical research.
- working knowledge of the relationship and regulatory obligation of the cro industry with pharmaceutical/biotech companies.
- familiarity with moderately complex statistical methods that apply to phase i-iv clinical trials.
**about our client**
join a team that works on groundbreaking compounds and profoundly impacts patients’ lives! our client is a distinct, full-service contract research organization with offices in california, massachusetts, and quebec. They are serious about scientific integrity and has a dynamic company culture, including a focus on work-life balance.
**value proposition for you**
- flexible work schedule.
- proven potential for professional growth.
- a community of brilliant minds at your disposal.
- the stability of working for a robust, financially sound cro that is growing at a sustainable pace.
- exposure to more than 20 therapeutic areas, including cutting edge therapies such as immuno-oncology, biosimilars, gene therapy, and new molecular entities.
Note: please attach your latest cv along with your response on zintro.
+18 Other Responses
