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You are testing hundreds of hypotheses with many t-tests. What considerations should be made?

What is a key disadvantage of the F-test when compared to multiple t-tests?

What is a key disadvantage of the F-test when compared to multiple t-tests?

Hundreds of Hypotheses

You are testing hundreds of hypotheses with many t-tests. What considerations should be made?

Let’s say that your company is running a standard control and variant AB test on a feature to increase conversion rates on the landing page. The PM checks the results and finds a .04 p-value.

How would you assess the validity of the result?

Experiment Validity

In an A/B test, how can you check if assignment to the various buckets was truly random?

In an A/B test, which of the following is a common method to determine if the assignment to the test groups was truly random?

In an A/B test, which of the following is a common method to determine if the assignment to the test groups was truly random?

Random Bucketing

Katalyst Healthcares & Life Sciences Salaries by Position

<h3>Job Description</h3>Katalyst Healthcares & Life Sciences is hiring entry-level candidates for several positions in contract research for clinical trials of drugs, biologics, and medical devices.We have a few immediate job opportunities available in Drug Safety, Pharmacovigilance, and Clinical Research fields. We work with university hospitals, pharmaceutical companies, and recruiting partners.<h3>Position Overview</h3>The Global Discovery Chemistry Analytical (GDC-AX) group at Client Institutes for Biomedical Research (NIBR) is seeking a team-oriented Scientist with an emphasis on bioanalytical technologies and laboratory automation for in vitro assays.<h3>Responsibilities</h3><ul><li>Daily operation and data interpretation of assays including high throughput equilibrium solubility, high throughput lipophilicity, shake flask solubility, and melting point determination.</li><li>Tuning of compounds on mass spectrometers, maintaining solutions for assays and bioanalysis, and performing assays on various liquid handlers/automation. Minor maintenance/troubleshooting of assay-related automation systems may be required.</li><li>Utilization of HPLC and mass spectrometry, including data interpretation.</li></ul><h3>Requirements</h3><ul><li>A good understanding of laboratory equipment, automation, and software is desirable.</li><li>Demonstrated experimental and problem-solving skills, excellent collaboration, and communication skills (written and oral), and an eagerness to learn.</li><li>Excellent time management skills and the ability to work in a team-based drug discovery environment.</li><li>BS/MS with 0-3 years in analytical chemistry, ADME, pharmaceutics, PK/PD, or related fields.</li></ul><h3>Additional Information</h3>All your information will be kept confidential according to EEO guidelines.
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<h3>Job Description</h3>Summary<ul><li>The Clinical Research Scientist (contractor) will work within the US Medical Affairs department and will be responsible for supporting the Scientific Director/Disease Lead within the hematology therapy area in developing medical affairs documents, contributing to ongoing medical affairs activities and clinical data review for ongoing MAST and registries. The specific activities will depend on the timing/needs of the specific team at that time.</li></ul>Primary Responsibilities:<ul><li>Assists Scientific Director and/or Disease Lead in making recommendations, taking action and providing medical input related to medical affairs projects.</li><li>Assists the Scientific Director and/or Disease Lead to interface with project team members including: Medical/Clinical Operations, Commercial, Data Management, Statistics, Drug Safety, Regulatory and Project Management.</li><li>Assists with review of data from ongoing MASTs and registries including: safety, primary/secondary efficacy variables, and laboratory data.</li><li>Assists with preparation of key medical affairs documents (i.e. tactics, ad board slides, etc).</li><li>Responsible for completion of milestones associated with specific projects (as assigned).</li></ul>Skills/Knowledge Required:<ul><li>Bachelor’s degree in science required (advanced science degree a plus).</li><li>Basic understanding of hematology therapeutic areas.</li><li>Maintain professionalism and confidentiality at all times.</li><li>Basic computer skills including Microsoft Office proficiency (e.g. Word, PowerPoint, Excel). Medical literature database searching skills and experience is a plus.</li><li>Self-motivation and flexibility with regard to daily attendance, assignments, and deadlines.</li><li>Excellent interpersonal skills (written and verbal) to work effectively and efficiently as part of a team.</li><li>Proficient at multitasking on multiple ongoing projects, with agility to course adjust/modify, and remain highly detail-oriented with timely deliverables.</li><li>Able to operationally function and communicate in a cross-functional matrix organization across various disease teams.</li></ul><h3>Additional Information</h3>All your information will be kept confidential according to EEO guidelines.
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<ul><li>Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.</li><li>We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.</li></ul><h3>Job Description</h3>Job Summary:<ul><li>The Clinical Research Scientist (contractor) will work within the US Medical Affairs department and will be responsible for supporting the Scientific Director/Disease Lead within the hematology therapy area in developing medical affairs documents, contribute to ongoing medical affairs activities and clinical data review for ongoing MAST and registries. The specific activities will depend on the timing/needs of the specific team at that time.</li></ul>Responsibilities:<ul><li>Assists Scientific Director and/or Disease Lead in making recommendations, taking action and providing medical input related to medical affairs projects.</li><li>Assists the Scientific Director and/or Disease Lead to interface with project team members including: Medical/Clinical Operations, Commercial, Data Management, Statistics, Drug Safety, Regulatory and Project Management.</li><li>Assists with review of data from ongoing MASTs and registries including: safety, primary/secondary efficacy variables, and laboratory data.</li><li>Assists with preparation of key medical affairs documents (i.e. tactics, ad board slides, etc).</li><li>Responsible for completion of milestones associated with specific projects (as assigned).</li></ul>Skills/Knowledge Required:<ul><li>Bachelor’s degree in science required (advanced science degree a plus).</li><li>Basic understanding of hematology therapeutic areas.</li><li>Maintain professionalism and confidentiality at all times.</li><li>Sufficient background of basic computer skills including Microsoft Office proficiency (e.g. Word, PowerPoint, Excel). Medical literature database searching skills and experience is a plus.</li><li>Self-motivation and flexibility with regard to daily attendance, assignments, and deadlines.</li><li>Excellent interpersonal skills (written and verbal) to work effectively as part of a team.</li><li>Proficient at multitasking on multiple ongoing projects, with agility to course adjust/modify, and remain highly detail-oriented with timely deliverables.</li><li>Able to operationally function and communicate in a cross-functional matrix organization across various disease teams.</li></ul><h3>Additional Information</h3>All your information will be kept confidential according to EEO guidelines.
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<h3>Job Description </h3>Title: Clinical Research Scientist Job Description <ul><li>Assist the Clinical Research Scientist team to interface with project team members including: Clinical Research Physician, Clinical Operations, Data Management, Statistics, Drug Safety, Regulatory and Project Management. </li><li>Review and query of oncology/hematology data including but not limited to: safety, primary efficacy variables, and laboratory data. </li><li>Assist with clinical document preparation (writing, reviewing, amending and cross-functional facilitation as appropriate). </li><li>Assist with clinical study report preparation to include narrative writing. </li><li>Participate in adhoc meetings. </li><li>Support clinical trial activities as requested. </li> </ul>Skills/Knowledge Required: <ul><li>Minimum 10 years experience in oncology/hematology clinical development. </li><li>Excellent written and verbal communication skills and interpersonal skills. </li><li>Knowledge of clinical trial design, basic statistics, and data review tools. </li><li>Proficient at data review and interpretation. </li><li>Experience in protocol development, study report preparation, Investigator Brochure preparation, regulatory submissions. </li><li>Full understanding of GCP and ICH Guidelines. </li><li>Detail-oriented, well-organized. </li><li>Ability to assimilate technical and scientific information quickly. </li><li>Proficient in Microsoft Office (Word, Excel, PowerPoint; Microsoft Project a plus), JReview, EDC (Rave). </li><li>Demonstrated ability to work as part of a team. </li><li>Oncology/Hematology experience (required); Registry experience (plus). Protocol authoring (plus). Data review and medical monitoring of data (required). </li><li>Qualifications: Advanced Degree in Life Sciences (e.g., nursing, pharmacy or related medical field), minimum 10 years' experience in clinical research development or equivalent. </li> </ul>#J-18808-Ljbffr

Responsibilities: <ul> <li> Collaborate closely with business stakeholders to gather and document requirements for regulatory operational projects. </li> <li> Analyze business processes and identify opportunities for improvement and automation. </li> <li> Develop and maintain detailed business requirements, process flows, and use cases. </li> <li> Work closely with project managers to ensure timely project delivery and adherence to project timelines. </li> <li> Create and maintain project documentation, including RAID logs and other relevant artifacts. </li> <li> Leverage key tools such as MS Office Suite, Jira, Lucidchart, and other project management tools. </li> <li> Understand and manage cross-functional dependencies across multiple initiatives. </li> <li> Contribute to validation deliverables for operational control centers and sprints. </li> </ul> Requirements: <ul> <li> Minimum of 5 years of Business Analyst experience in the life sciences industry. </li> <li> Strong GxP regulatory knowledge and experience. </li> <li> Proficiency in MS Office Suite, Jira, Lucidchart, and other project management tools. </li> <li> Veeva RIM (preferred, not required). </li> <li> Ability to work independently and as part of a team. </li> <li> Strong analytical and problem-solving skills. </li> <li> Experience with Agile methodologies (preferred, not required). </li> <li> The candidate should have an EXCELLENT Communications skills. </li> </ul>

Katalyst Healthcares & Life Sciences Interview Questions

Katalyst Healthcares & Life Sciences Interview Guides

Katalyst Healthcares & Life Sciences Interview Questions

Katalyst Healthcares & Life Sciences Salaries by Position

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