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I am organizing a controlled clinical study to measure how an oral curcumin supplement influences both recovery and bioavailability in a herd of more than 20 horses. I need a veterinary research professional who can shape the entire protocol from start to finish. Key tasks • Draft a scientifically sound study design outlining objectives, hypotheses, inclusion/exclusion criteria, treatment groups, dosage schedule, and wash-out periods. • Define clear metrics for recovery (e.g., muscle enzyme profiles, lameness scores, heart-rate variability) and bioavailability (e.g., plasma curcumin concentration, AUC, Tmax). • Create a sampling timeline and specify required laboratory assays. • Prepare all study documentation: informed consent forms for owners, animal ethics committee application, SOPs for dosing, sample handling, data collection sheets, and adverse event reporting. • Recommend statistical methods and power calculations suitable for the cohort size (>20 horses). • Outline practical logistics—stable requirements, feed controls, randomization, blinded assessments—and identify any specialized equipment. • Deliver a concise plan for data analysis and final reporting templates. I will supply background literature on equine curcumin studies and have access to a cooperating equine clinic. Your deliverable will be a complete, ready-to-submit protocol package (Word + PDF) that the clinic staff can follow without additional clarification. Veterinary clinical research experience—preferably in equine nutrition or musculoskeletal recovery—is essential. Familiarity with GLP guidelines and statistical software such as SAS or R will be highly valued.
Project ID: 40476819
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28 freelancers are bidding on average €13,518 EUR for this job

With over a decade of pioneering work in veterinary research, particularly in equine nutrition and musculoskeletal recovery, I am well-positioned to shape a comprehensive protocol for your controlled clinical study. I operate from a vantage point of ownership and thoroughness; knowing that the smallest oversights can substantially undermine the outcome of any study, I will draft a scientifically sound study design that leaves no room for ambiguity. I am deeply familiar with GLP guidelines and skilled at using statistical software like SAS and R - three key requisites for this particular assignment. Moreover, my team specializes in data analysis, research writing, scientific writing, and statistical analysis—all definitive interests in this project. You need not to worry about the vital SOPs or adverse event reporting as they are part and parcel of any research we conduct. In vetting for a partner who can not only keep up with but effectively set up systems for a project of this magnitude while seamlessly following through on all necessary protocols and expectations, my team and I stand unrivaled. At A2Z Research Consultants, we epitomize "research" in our practice by ensuring that every aspect is thoroughly planned out, noting the slightest detail while maintaining forward momentum so as to deliver quality results at the specified milestones. Looking forward to a successful collaboration on this exciting endeavor!
€20,000 EUR in 60 days
8.1
8.1

With my seasoned and prolific academic medical writing background, your Equine Curcumin Clinical Study Design project falls perfectly within my areas of expertise. Over the years, I've produced top-notch research papers and theses, aligning my writing with the exacting standards of academia. My capability to analyze intricate information, synthesize different perspectives, and present arguments in a clear and logical manner will be greatly beneficial in shaping your entire clinical study protocol from start to finish. In addition to being highly experienced in crafting comprehensive academic materials, I also possess a keen eye for detail that proves valuable in proofreading and editing. This meticulous attention to detail is vital for eliminating errors and ensuring an exemplary quality outcome—a trait that's particularly crucial for a project as stringent as yours. Moreover, my unwavering dedication to continuous learning ensures I remain apprised on the latest research trends. Consequently, I can incorporate the most current data and insights into your protocol design to maximize its potential for obtaining accurate results. Choosing me for this project guarantees you an astute researcher who is adept at handling exclusive sci
€10,000 EUR in 7 days
6.7
6.7

With your project on a controlled clinical study to assess the impact of an oral curcumin supplement in horses, my deep knowledge and hands-on experience in data collection, research writing, and statistics make me an ideal candidate for this work. Equipped with a Ph.D. in AI and machine learning, I have over a decade of experience designing and executing complex studies, including those in voice recognition, surveillance, and automated workflows. This translated expertise lends freshness to the table when evaluating the potential use of curcumin in equine nutrition or musculoskeletal recovery. In conclusion, I offer not just the prowess you seek but also a demonstrated history of using these skills effectively—content creation for major organizations like Unilever Pakistan and State Bank of Pakistan—as well as an understanding of GLP guidelines. With my proactive approach, unwavering commitment to quality, and the convenience of being acquainted with your required skill set like statistical analysis for cohort size greater than 20; I am confident in my abilities to produce deliverables that exceed your expectations.
€10,000 EUR in 30 days
6.7
6.7

As an experienced researcher, I have a solid understanding of statistical analysis using software such as SAS or R, an ability that would prove highly beneficial in this equine clinical study project. I am well-versed with the Global Laboratory Practice (GLP) guidelines that underscore the importance of efficient study design and protocol documentation which you seek diligently. While I might not have direct experience in equine nutrition or musculoskeletal recovery, my expertise in scientific research is quite suited to this project. My approach is comprehensive, meticulous and detail-oriented ensuring that no aspect is overlooked. Rest assured, I'd utilize the background literature you provide diligently and adapt it to design a robust protocol taking into account all the relevant parameters including stable requirements, feed controls and randomization. Moreover, having provided virtual assistance and having supported businesses with ongoing site maintenance and performance optimization, I can provide insights not just on the scientific aspects but also operational aspects, ending in the delivery of a complete and ready-to-submit protocol package for your clinic staff to implement with clarity. So let's team up! Together we can open new doors in equine nutrition research.
€10,000 EUR in 1 day
5.9
5.9

I understand you need a comprehensive, scientifically sound study design for your controlled clinical study on oral curcumin's influence on recovery and bioavailability in over 20 horses. My experience includes designing and executing similar equine research protocols, including one that successfully elucidated the pharmacokinetic profile of a novel oral supplement in a target herd size. I will draft a detailed protocol covering objectives, hypotheses, inclusion/exclusion criteria, treatment groups, dosage schedule, and wash-out periods. For recovery metrics, I'll define specific protocols for collecting and analyzing muscle enzyme profiles, administering standardized lameness scoring systems, and implementing heart-rate variability measurements. Bioavailability will be assessed through precise plasma curcumin concentration analysis using liquid chromatography-mass spectrometry (LC-MS) at defined time points. What is the target duration for the wash-out period following any prior supplementation or strenuous activity before the study begins? Ready to start as soon as you confirm scope.
€17,100 EUR in 21 days
5.2
5.2

Hi there, I understand the importance of well-designed and meticulously executed scientific studies for impactful results. With my strong background in clinical research,study design and data analysis, I am certain that I am the right fit for your study. I hold a degree in Biostatistics and have significant experience in study design and data analysis within medical research. Being an Egyptian pharmacist, I also have specific knowledge in equine nutrition and musculoskeletal recovery which would perfectly complement your project needs. Throughout my career, I have designed, conducted, and analyzed numerous epidemiological studies and clinical research projects using a range of statistical software including SPSS and R - precisely what you need for this study. My repertoire also includes robust statistical analysis methods such as ANOVA, linear & logistic regression, survival analysis etc., ensuring sound conclusions are drawn from the collected data. Additionally, I take pride in my ability to present complex findings in a manner that is both accessible and compelling to non-technical stakeholders. As a result, you can rely on me to provide you with not just a ready-to-submit protocol package but also clear visualizations of data that will facilitate effective communication of your findings. Let’s turn your curcumin study into a story that is informative and actionable. Best wishes, Hossam Khater
€15,000 EUR in 90 days
4.5
4.5

Your goal of meticulously quantifying curcumin's impact on equine recovery and bioavailability is directly analogous to my experience designing protocols for novel therapeutic interventions in large animal populations, where precise pharmacokinetic analysis and objective outcome measures were paramount. I've successfully implemented similar study designs that yielded statistically robust data for publication. My approach will involve establishing clear, measurable objectives aligned with your desired outcomes. I'll draft a detailed protocol encompassing robust inclusion/exclusion criteria, stratified randomization into treatment and placebo groups, and a precisely defined curcumin administration schedule with appropriate wash-out periods. For recovery, we'll leverage validated lameness scoring systems, serial muscle enzyme panels (CK, AST), and heart rate variability analysis. Bioavailability will be assessed via validated LC-MS/MS quantification of plasma curcuminoids at strategic time points post-administration. To ensure optimal alignment, what are your primary concerns regarding potential confounding factors in a herd setting? Furthermore, what is the projected timeline for this study's initiation? I'm available to discuss these details and further refine the protocol to meet your specific research needs.
€17,100 EUR in 21 days
4.0
4.0

Hi there, As an experienced professional in Data Analysis, Research, and Statistical Analysis, I find this project both intriguing and aligning with my skillset. Although my profile primarily emphasizes on technical domains, it's worth mentioning that I also have a proven track record of academic research that involved careful planning and thorough consultations to implement effective methodology. In addition, my proficiency with statistical software such as SAS or R would enable me to make valid inferences from the extensive field data you have. My ability to understand complex scenarios and devise precise strategies will contribute significantly in your study design. I can formulate a scientifically-sound study design by outlining objectives, hypotheses, inclusion/exclusion criteria, treatment groups, dosage schedule, and wash-out periods. Moreover, I will define suitable metrics for recovery and bioavailability while working closely with you to customize them to your requirements - like muscle enzyme profiles, lameness scores or heart-rate variability for tracking recovery progress.
€15,000 EUR in 3 days
3.9
3.9

Hi Your project goes far beyond a literature review—it requires a complete, clinic-ready protocol package covering study design, ethics documentation, operational procedures, statistical planning, and final reporting for an equine curcumin clinical study. What you’ll get: * Comprehensive study protocol with objectives, hypotheses, treatment arms, dosing, and washout design * Recovery and bioavailability endpoint framework * Sampling schedules and laboratory assay recommendations * Ethics application support and owner consent documentation * SOPs for dosing, sample handling, data collection, and adverse event reporting * Statistical analysis plan, power calculations, and reporting templates * Practical implementation guidance covering randomization, blinding, feed controls, and clinic workflow I’m a verified freelancer and I’ve completed similar research-intensive projects with 5⭐ feedback for accuracy and delivery. Timeline: 10–14 days for a complete protocol package with revisions. Budget: €12,500 EUR Please send me a message so we can get started immediately.
€12,500 EUR in 10 days
2.4
2.4

altea, Spain
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Member since May 14, 2026
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