Life Science Procurement Maturity
We are a global research and advisory firm and are seeking experts who can assist us with insights (both qualitative and quantitative) on the maturity of procurement as a function across countries / regions.
This entails providing us with comparative data / benchmarks that help indicate the maturity of countries in terms of their procurement practices. The applicable industry is life sciences.
The list of regions and countries include:
in western europe: germany, france, uk, holland, spain, italy, switzerland, belgium, (norway & finland nice to have but not mandatory)
in apac: india, china, singapore (australia nice to have but not mandatory)
in latam: brazil, argentina, colombia, mexico
we would like to engage via phone consult with experts knowledgeable on the aforementioned topic.
We are looking for a phone consult for a time period of 1-2 hours to discuss the same. Please supplement your expression of interest with an indication of the approach that you are likely to adopt to answer the aforementioned question.
Regards,
budha
+13 Other ResponsesPharma Qualitative Study
We are seeking highly specialized experts with experience in the life sciences industry - must meet below specifications
location: usa - san fransisco bay area, los angeles, philadelphia, new york, boston.
Industry: pharmaceuticals, contract development and manufacturing organizations (cdmos)/clinical research organizations (cros), and life science market research.
Testing availability: late june - early july
study 2: qualitative study - one on one either telephonic or in-person interviews
**respondent profile**:
cost estimates for both tdi (telephonic interviews) and idi (in person interviews) with 8 respondents, 2 each from clinical trial supply managers/coordinators/directors, procurement contacts / outsourcing managers / directors, clinical / pre-clinical teams, senior executives (pharma/biotech/cro)
**expert's job titles**:
1) clinical trial supply managers / coordinators / directors
2) procurement contacts / outsourcing managers / directors
3) clinical / pre-clinical teams
4) senior executives
**experts must have a clear understanding of the following topics (doesn't have to be an expert at each level, but at least one, also a basic understanding of others)**:
a. Api services & chemical development – all stages of drug development for small molecules, potent and cytotoxic compounds, and peptides
b. Pharmaceutical development – development cycle of clinical candidate into an optimum formulation and clinical stages manufacturing
c. Analytical services – analytical services supporting drug substance (api) and drug product development including cmc regulatory filings
d. Clinical trial supply – clinical supplies, packaging, distribution and delivery of clinical protocols, supply chain management.
E. Clinical technologies - solutions for patient enrollment, screening randomization, drug assessment etc.
F. Commercial services – api supply, manufacturing, testing and packaging to end-user distribution.
+18 Other ResponsesClinical Trials Ai Platform
We are looking for experts who can provide their insights and feedback to a startup seeking equity investment.
Startup description:
design & conduct better clinical trials. Making clinical trials seamless by bringing together the best and most important functionality of study design & protocol optimization, trial administration, data collection & task management all in one intelligent system.
Experts that have interest, knowledge or background in:
industry:
healthcare, clinical trials, pharmaceutical, life sciences, health and wellness
technology:
healthcare it, deep learning, ai, end-to-end platforms
who we are:
we are an online investment platform working to provide a fair and transparent process for startup evaluations and that selects the companies that will outperform other startups in the next three to ten years.
Who you are:
you do not need to be an experienced angel investor to be a valuable member of the evaluation team. We seek a diverse group with expertise that may cover the market, business model, technology and customers of the startup company. However, if you are an accredited investor, you have the option (but not an obligation) to invest as little as $1000 fee- and carry-free in the startup company if the resulting evaluation leads to an investment.
What you will do:
as a participating evaluation team member, you will answer a set of questions and rate the comments and feedback of other evaluators.
(this is an all volunteer community of industry experts and investors that evaluate startups, requiring about 2 hours total of your time over about 2 weeks.)
what’s in it for you:
- an inside look at cutting-edge technology or go-to-market approaches
- introductions to company management, upon request
- collaboration with like-minded experts who are on your evaluation team
- contributing to creating a fairer, more-informative process for startups seeking investment
+29 Other ResponsesLife Sciences
Consultant position in life sciences management consulting for phd in science
+21 Other ResponsesInformation Technology Trends In Life Science
Dear experts,
i am writing on behalf of a consulting firm that conducts expert interviews in support of industry-wide studies for many of the world's fortune 1000 companies. We are an authorized zintro partner.
For a current study for a professional services provider, we are interested in learning about key business issues and priorities, interest in types of work and perspectives on the future of it (application, architecture, cloud, digital) in the life science industry (pharma, medical devices).
We need to speak with senior experts who are either currently or have recently (within 1 years) been employed in it positions at global top 20 pharma or medical devices companies. Experts should have 15+ years of industry experience.
Please note that we are not looking for any confidential information but rather high-level information to understand where the industry is headed from an it perspective.
We are scheduling 45-60 minute discussions this week and next, and we are happy to compensate you for your time.
Look forward to hearing from you!
best regards,
julian
+4 Other ResponsesZintro Webinars
We are hosting webinars presented by zintro experts as a way to source new clients for you. We promote the webinar invitation to our 180,000 users through email and other channels, then we post the webinar to our blog and promote the video. You can view some examples here.
This initiative would be completely free for you. You would be able to include your zintro profile in the webinar to promote your services and you would only pay us 15% of any engagement generated through the webinar effort.
Presentations are normally 40 minutes and focus on subjects that might showcase your expertise and help you source new clients. After your presentation, we will leave an additional 15 minutes of time to answer attendee questions live.
To view some examples of past webinars, go to: https://blog.Zintro.Com/webinars/
i'm coordinating the schedule for the next available webinar slots and would like to know if you are available for any of the following dates:
july 16th, 2015 1:00 pm edt
july 30th, 2015 1:00 pm edt
august 13th, 2015 2015 1:00 pm edt
august 27th, 2015 2015 1:00 pm edt
september 10th, 2015 2015 1:00 pm edt
september 24th, 2015 1:00 pm edt
october 8th, 2015 1:00 pm edt
october 22nd, 2015 1:00 pm edt
november 5th, 2015 1:00 pm edt
november 19th, 2015 1:00 pm edt
december 3rd, 2015 1:00 pm edt
we usually hold a practice session on the monday preceding the presentation date. We can do the practice session at whatever time is most convenient for you.
In addition to your preferred dates, i would appreciate if you could provide the following information:
1) zintro id or sign up email address
2) complete name and title
3) company you work for
4) topic of your presentation
+27 Other ResponsesPharma Research Interviewees
We are seeking highest specialized experts with experience in the life sciences industry - must meet below specifications
location: usa - san fransisco bay area, los angeles, philadelphia, new york, boston.
Industry: pharmaceuticals, contract development and manufacturing organizations (cdmos)/clinical research organizations (cros), and life science market research.
Testing availability: late june - early july
study 1: qualitative study - focus group interviews with 3 groups (6-8 respondents per group)
**respondent profile**:
group 1: 6-8 pharmaceutical executives from top 20 biotech companies who are influencers, contributors or decision makers on outsourcing services to contract development and manufacturing organizations (cdmos)/clinical research organizations (cros).
Group 2: 6-8 pharmaceutical executives from top 10 clinical research organizations (cros) companies who are influencers, contributors or decision makers on outsourcing services to contract development and manufacturing organizations (cdmos)/contract research organizations.
Group 3: 6-8 pharmaceutical executives from small / mid-sized pharmaceutical companies who are influencers, contributors or decision makers on outsourcing services to contract development and manufacturing organizations (cdmos)/contract research organizations.
**expert must have** a clear understanding of the following topics (doesn't have to be an expert at each level, but at least one, also a basic understanding of others):
a. Api services & chemical development – all stages of drug development for small molecules, potent and cytotoxic compounds, and peptides
b. Pharmaceutical development – development cycle of clinical candidate into an optimum formulation and clinical stages manufacturing
c. Analytical services – analytical services supporting drug substance (api) and drug product development including cmc regulatory filings
d. Clinical trial supply – clinical supplies, packaging, distribution and delivery of clinical protocols, supply chain management.
E. Clinical technologies - solutions for patient enrollment, screening randomization, drug assessment etc.
F. Commercial services – api supply, manufacturing, testing and packaging to end-user distribution.
+15 Other ResponsesLife Science Venture Capital
Request for expert discussion on future of medical devices
dear experts,
we work with industry experts to support industry studies for many of the world's fortune 1000 companies. We are an authorized zintro partner.
For a current study, we are interested in understanding emerging trends and transformational technologies that may impact the medical device industry in the future. We are only interested in shared industry learnings and are not looking for any confidential information.
More specifically, we are interested in speaking with experts that have deep expertise/experience with the following:
- investment ventures within life science
- venture capitalist firms
- corporate vc's
- experience with visionaries and product directors at large medical device enterprise companies
please note that we are only interested in personal point of view and shared learnings to the extend possible. We are not interested in and able to accept any confidential information. Our practice is to keep your identity anonymous, as well as that of our client.
We are scheduling 45-60 minute discussions with experts, this week and parts of next week (july 10th), and we are happy to provide a flexible usd 250 compensation for the interview.
If you kindly let me know your contact details (email, phone/skype), i could provide more specifics on the study and standard process.
We would welcome any referrals to other relevant experts as well.
Thank you in advance, and we are looking forward to hearing from you.
Best regards,
meagan
+37 Other ResponsesSas Programmer Life Sciences
Full time individual
minimum 5 years sas programming experience in pharmaceutical industry/cro in the us or eu.
• 7 years experience strongly preferred.
• strong knowledge and solid understanding of clinical trials.
• able to critically review protocol, statistical analysis plan for statistical/programming needs. Experience in programming of statistical outputs a must.
• experience with regulatory submissions and integrated summaries. Extensive experience with validating outputs of others.
• proficient in sas macro, cdisc, sdtm, and adam.
• strong programming, analytical, project management, verbal, written communication skills.
• track record of successful management of technical projects like e.G . Leading programming for assigned clinical studies.
• able to work with minimal supervision.
• effective under pressure: can meet timelines and provide high quality deliverables.
+13 Other ResponsesLife Sciences Online Training
We are a leading provider of educational webinars for the international life sciences community and we are looking for independent u.S.-based consultants/subject matter experts with a minimum of 10 years hands-on industry experience to provide interactive, online training for the pharmaceutical, biotech and/or medical device industry.
Must have proven experience in instructional design and content development and be well versed in adult learning principles. This position may lead to a long-term contract.
+24 Other ResponsesLife Science Logistics
We are looking for experts who can assist with a query on "life science logistics". The scope of this request is as follows:
1) market scenario - major players, their clients, and specialties
2) industry best practices - engagement models, single/multiple supplier engagement etc.,
3) cost saving opportunities - cost breakup of life science logistics, cost saving opportunities.
A detailed questionnaire would be shared with shortlisted experts.
+12 Other ResponsesPharmacovigilance Business Development
Job title: business development manager
job location: open (us and uk)
job type: full-time
please note: this position is only open to u.S. And u.K residents seeking full-time employment. No consultants please.
Position summary:
will work collaboratively with other colleagues to increase sales within the life sciences industry. Responsibilities will include full cycle sales including; researching, identifying, cold/warm calling, getting client meetings, listening and understanding client needs, addressing client concerns/objections, proposing solutions, negotiating, obtaining sows and closing the deal. Are expected to quickly develop credibility with customers/prospects and build trust through professionalism and knowledge of our services and products.
**essential duties and responsibilities**:
- prospect accounts focusing on safety related to our products and services
- identify and develop new accounts and following up on existing leads
- develop and maintain positive and productive relationships with key target accounts
- manage assigned accounts to generate both incremental and repeatable annual business
- initiate and manage rfi and rfp process and negotiate terms for all account programs and projects
- work collaboratively with the services organization to ensure a complete and professional delivery of our software and service solutions
- collaborate with our executives and smes to maximize account coverage
- maintain knowledgeable understanding of changing regulatory guidelines and mandates affecting the industry community
**job experience and qualifications**:
- must demonstrate a sustained (7+ years) and successful track record selling professional services to pharmaceutical, biotech, medical device, and/or clinical research organizations.
- selling drug safety consulting services and products is desired.
- candidates should exhibit an understanding of the regulatory pharmacovigilance process for both pre-marketed and post-marketed stages of a product.
- experience working with regulatory affairs departments, product safety related departments, or regulatory submissions is highly desired.
- experience with data-mining or statistical signal detection products is desirable.
- demonstrated track record of success working with senior level management in a fast paced growth environment is essential.
- full sales cycle experience is required (prospect, identify opportunities, propose solutions, negotiate, close).
- strong, quality-oriented proposal writing and proposal management experience.
- ambitious, driven and self-motivated personality is required.
- college degree or equivalent experience required.
- willing to travel throughout the us, estimated up to 80%.
- background in software as a service (saas) market is preferred.
**we offer**:
- competitive base salary + commission.
- benefits: 100% medical/dental for employee and his/her family.
Interested applicants should reply with a brief summary of their relevant experience and attach their latest cv on zintro.
Please note: this position is only open to u.S. And u.K residents seeking full-time employment. No consultants please.
+49 Other Responses
