Clinical Research Organization (cro)
My firm is looking to speak to an expert in contract/clinical research organizations. Must have knowledge about setup, operations, quality controls marketing, and pr.
+24 Other ResponsesCro Outsourcing In Clinical Trial
We are a market research company looking for the following information pertaining to cros on behalf of our client:
unique cro outsourcing trends in the clinical trial (cro) industry where cros have been innovative in how they offer services to pharmaceutical companies; real life examples between cros and pharmaceutical companies
preferred or approved supplier for major pharmaceutical companies
how other pharmaceutical companies validate cro rates without going out to bid?
Supplier analysis and market analysis
+24 Other ResponsesClinical Research Associate
Hi, i am looking for the following details on japan cro market.
1. How has the cra market changed during 2010-2013 and how is it going to be in next 2 years
2. Market cost for cras
3. The biggest challenge for japanese cros and global cros over the next 2-5 years
3. Will clinical trials in japan continue to rise?
4. Potential changes in regulations that will change the way that approach cro business
+4 Other ResponsesPharma Clinical Research Moderators
We are seeking a highest quality experienced moderator with experience in the life sciences industry - must meet below specifications
moderation 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
hello, we are conducting market research on outsourcing partnering decisions for a major cdmo/cro. For the qualitative part of the research we are looking for a seasoned moderator with the following specifications to conduct in-person focus group interviews (6-8 pharmaceutical executives who are outsourcing decision makers) at a facility.
1. Minimum 15 years experience with bio-pharmaceutical research and manufacturing, especially contracting with contract development and manufacturing organizations (cdmos) / clinical research organizations (cro) - flexible on years of experience.
2. Minimum 5 years experience with moderating qualitative focus group interviews - flexible on years of experience.
3. Moderating certification required.
4. A clear understanding of the following topics
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.
5. Flexibility to travel to facility location.
If you are interested and fulfill the above requirements, please contact us immediately with your profile, a brief summary, rates and confirmation of availability.
+16 Other ResponsesClinical Research Organization
Hello,
we are a prominent nyc-based expert network and an authorized zintro partner
our client has an immediate need to conduct phone consults with multiple experts knowledgeable about contract / clinical research organization (cro) industry. More specifically, they are hoping to better understand the overall market growth, trends & outlook, as well as key segments.
Here's more information on the type of people they are looking to speak with:
• a cross-section of pharma and biotech players of different sizes
o expert must have ownership of development pipeline
o have expertise related to key large/growing tas (therapeutic areas) and regions – initial hypothesis is focused on oncology, infectious diseases/vaccines, immunology
o we would probably like to speak to mostly us players, some european and a couple in asia
• sponsor members who own (or influence) outsourcing decisions (e.G., operations, clinical research)
• cro members responsible for strategy/planning and pricing decisions
• potentially across other segments of the value chain
thanks,
tj
+19 Other ResponsesBusiness Development For Contract/clinical Research Organisation
Looking for an expert to help in business development strategies and tactics for a niche cro (contract/clinical research organisation), specifically as it relates to exploiting scientific expertise and connecting to scientific decision makers in pharma and biotech
+18 Other ResponsesContract Research Organizations
We would like to speak with an expert who can help us in gathering the information on cros direct cost data for specific cro services. We would like to cover cost per site and cost per patient estimates based on the following parameters:
geographical focus: north america and western eu
services required:
• site feasibility
• site identification
• site qualification
• site initiation
• essential document collection
• site management
• site monitoring
• project management
+15 Other ResponsesBiotech And Cro Partnership
I am looking for someone with deep experience in biotech and cro strategic partnerships to help facilitate, plan and establish a the partnership process.
+19 Other ResponsesClinical Research Organization (cro)
**please respond to the following request with a proposal if:
1) you currently, or within the last year, work at a pharmaceutical or biotech firm.
2) you are familiar with phase 1 clinical trials.
Familiarity with and understanding of how biopharma and pharmaceutical companies decide which cros to use for early stage phase 1 clinical research. Will be able to speak to growth trends related to spending on r&d in industry and spending on cro services. To the extent possible, will be able to speak to how this may differ for innovator versus generic drugs. Will be able to speak to the reputations of different cro service providers for early stage phase 1.
1) how has your spending on cro early stage services trended in the past few years? What is your outlook for demand for cro services? Why? To the extent you can speak to this, how has this differed for generic vs. Innovator drugs?
2) what is the decision process for determining which early stage phase 1 cro to use?
3) what factors are considered when determining which early stage phase 1 cro to use?
4) what are the early stage phase 1 cros that come to mind? Which cros have you considered? How do cro reputations differ across the different stages of clinical research (early vs. Late)? For different clinical services?
5) what are the trends for early stage phase 1 cro services moving overseas?
Areas of expertise:
seeking experts with knowledge of clinical trials, phase 1-4; clinical trials; early clinical research; cro; early stage clinical research; cros; clinical research organization; clinical research
+7 Other ResponsesVice President, Biometrics
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. Due to their growth and investment they have recently relocated our headquarters to southborough, ma. They are serious about scientific integrity and have 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.
As the vice president, biometrics you will…
* be a critical part of the global core leadership team by being responsible for the guidance and strategic direction of the global biostatistic and data management teams.
* advance the overall success and future growth of our client by having executive contact with current clients, providing key client oversight and strategic project contribution, and contributing to new business development.
* develop and implement department strategies to increase productivity and quality, while decreasing cycle times and costs. Oversee the data management and statistical aspects of client projects and project teams.
* participate in presentations of capabilities and research proposals to prospective clients. Represent data management and biostatistics in marketing efforts by developing project bid proposals, participating at bid defense meetings, or performing client presentations.
* provide oversight of the hiring and management of personnel. Ensure that adequate training occurs and that performance evaluations are completed.
* and much more!
education:
degree in statistics, biostatistics, math, or a related field. Phd or master’s degree preferred.
Experience:
* at least 15 years of relevant work experience and at least 5 years of supervisory experience.
* experience in a leadership position within biostatistics or data management for a cro.
* have previously contributed to the overall strategic direction of a company or business unit.
* 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.
+27 Other ResponsesLife Sciences-cro
Life sciences - croour company is a digital print,promotions and fulfillment company serving fortune 1000 clients. For the past 10+ years , through the research support division, we have worked with a 2b in revenue nc based cro providing site support materials (regulatory binders, mini protocols, etc) and patient retention programs. As a solutions vs product sale our margins are substantially higher than industry average. We has developed a level of sophistication required to meet the exacting standards and timelines required by both sponsors and the fda. Barriers to entry for new accounts/opportunities has been difficult at best owing to the decentralized nature of purchasing. We are discussing spinning off the research support group and would consider an opportunity to partner (equity basis?) with a life sciences/cro industry executive/consultant to increase our footprint in the clinical trial management space. all inquiries will be held in the strictest of confidence.
+9 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 Responses
