Pharmaceutical Products Deformulation
Hi there. I am looking for experts in deformulation in particular skincare products. I would also like to find someone who can analyse and quantify ingredients within the formulation?+7 Other Responses
Clinical Laundry Service In Uk
I looking for information pertaining to clinical laundry service cost across uk specific to norfolk and norwich area.+undefined Other Responses
Clinical Trial Logistics
Please let me know if you would like to provide consultation for the scope mentioned below
we are looking for experts in clinical trial samples logistics (global) who can comment on the below mentioned points
1) market scenario (key vendors, market trends etc.,) in transport and warehousing for clinical trial samples and ancillary materials)
2) industry best practices in sourcing
- sourcing best practices in transport and warehousing of clinical trials samples
- cost components break-up, cost drivers
- negotiation levers
please note that this is only a high level scope and we will share a detailed questionnaire after the initial introductory call+11 Other Responses
Clinical Quality Assurance
We're looking for a clinical quality assurance auditor:
1. Gcp or gxp auditing experience in a cro, pharma, or biotech setting.
2. The ability to travel
3. General knowledge of regulations: 21 crf part 11, gcp guidelines & standards.
-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 a clinical quality assurance auditor you will:
-assure that processes, quality systems, and inter-location synchronization within are aligned to promote an efficient working environment that follows compliance to regulations, standards, and good gcp guidance and provides clear pathways for inquiry, reporting, and resolution through audit, the capa process, and quality metrics.
-serve as liaison for quality compliance to all locations providing oversight from a corporate level.
-write and issue audit reports and communicate audit findings to relevant project team members and/or functional area management. Administrate the controlled documentation program by reviewing, revising, and writing sops.
-identify inefficient or outdated working procedures, develop revision plans, and conduct future review to determine the success of the procedure modifications.
-travel to multiple locations to conduct internal audits. Travel to suppliers to conduct vendor qualification and assessment audits.
-bachelors degree in a science or related field.
-at least 3 years of cro or pharma related experience.
-at least 2 years of relevant gcp auditing experience in a pharma, medical device, cro, or similar environment.
-general knowledge of relevant regulations including 21 crf part 11 and gcp guidelines and standards.
-asq-cqa or similar certification desired.+33 Other Responses
I'm looking for a biochemist who is mostly into cosmetics from body lotions to face creams and topical medication+5 Other Responses
Clinical Development Patient Recruitment
We are looking for a clinical development patient recruitment expert who can help us validate some data about the industry. I have the cost components, cost break down, cost drivers and % budget allocation for patient recruitment & retention. Can this be validated and corrected if not right?+undefined Other Responses
Clinical Nurse Leaders
Looking for clinical nurse leaders (cnl) or nurse hiring managers who can speak to the cnl position. I'm looking for a phone consultation to better understand who is hiring cnls, perceptions of the position, and expectations for job demand in the future.+19 Other Responses
Clinical Laboratory Improvement Amendments
Looking for a consultant knowledgeable in clinical laboratory improvement amendments (clia). Expert should be able to guide laboratory in all aspects of clia compliance.
Preferably located in the mid-west united states but open to the possibility of a consultant elsewhere within the us.+12 Other Responses
Looking for subject matter experts / consultants in clinical research, clinical trial, risk management, audit and inspection, gcp, clinical outsourcing, trial design and management,ethics fraud and misconduct, patient recruitment , documentation and management, clinical laboratories, facility/hospital , hospital clinical compliance, billing and coding for clinical services , patient/third-party coding and billing, sponsors, cros, clinical quality control/cqc for speaking engagements with over 25+ years of experience. Feel free to reach out to me.+20 Other Responses
Clinical Trials + Data
We are looking for experts in "clinical trials + data" to provide commentary and insights towards a startup that developed a data exploration platform that empowers critical insights to improve the accuracy and efficiency of research decisions.
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!+undefined Other Responses
Cro 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 Responses
Clinical Research Regulatory Service
• study objective:
to assess the clinical research consulting space with special emphasis on independent review board (irb) services. The aim is to understand the dynamics in the service/product offerings (regulatory compliance, medical writing, strategic affairs, electronic consent manager, meeting scheduler etc.). In addition, we would also like to understand the market overview of irb services comprising of market size, recent trends, drivers, barriers, etc. Focus would be to understand the customer needs, competitive landscape, pricing and market landscape for irb consulting services (regulatory compliance, medical writing, strategic affairs etc.).
• following are some of the key questions:
o what are the different services offered under regulatory consulting in clinical research?
O who are the key users / customers of regulatory consulting services?
O what are the needs for these services of different customers
o what are the factors that influence the customer’s purchase decision of consulting services / products?
O who are the top players providing consulting services and what is their market share?
O what are the billable rates charged on an hourly basis by the companies?
O why, if at all, do the rates differ across various services?
O are there different rates for different customer types? What are the reasons?
O how is the pricing structured for software products such as electronic consent form, meeting scheduler etc.?
o what are the key market trends, growth drivers and barriers to growth etc.?
o where are the key opportunities within the regulatory consulting market?
Preferred expert should meet the following criteria:
o location: us
o industry experience of 15+ years in the clinical research industry
o worked in coordinating clinical trials, device trails and observational studies, regulatory & irb submission, recruitment, data collection and input, source documentation creation, and overseeing good clinical practices (gcp) and ich guidelines
o understanding of clinical studies to ensure compliance with ich/gcp guidelines and federal regulations
o knowledge of regulatory consulting services as well as software offerings specific to clinical trial / research
o understanding of purchase process and pricing structure of consulting services+12 Other Responses