Average salary: $207,500 /yearly
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- ...budgets, support change in scopes and work on contract development with established templates. Previous experience in contracts within a CRO environment is required. Key Accountabilities Prepare and able to finalize in a client-ready format draft contract document,...SuggestedRemote jobContract workWork from home
$60k - $90k
...of experience in a regulated environment is required. Seniority Level Associate Employment Type Contract Job Function Information Technology Industries Pharmaceutical Manufacturing Location Louisville, KY Salary $60,000.00 - $90,000.00 #J-18808-Ljbffr Katalyst CROSuggestedContract work- ProTrials is a women-owned, WBENC-certified Contract Research Organization (CRO) that has been a trusted partner in clinical research since 1996. Founded with a clear mission to deliver high-quality, experienced, and ethical services, we’ve supported research behind innovative...SuggestedContract workInterim roleWork at office
$121.1k - $181.13k
...distribute global synonym lists for clinical data. Provide consultation, leadership, and expertise to Contract Research Organization (CRO) personnel and internal Data Managers on coding processes. Maintain OPDC coding guidelines, updating as necessary with input from...SuggestedContract workTemporary workLocal areaFlexible hours- ...plans (e.g., timelines, budget, risk, and quality plans) May manage the study start up process in countries assigned and/or oversee the CRO responsible for these activities as applicable Liaises with SCP, Lead SCP, Site Activation Partners and regulatory colleagues in...SuggestedContract workLocal area
- ...This role is responsible for driving discoverability, usability, and conversion performance through a coordinated approach to SEO, UX/CRO, web development, and content enablement. This role serves as the enterprise owner of organic acquisition and on‑site experience,...Suggested
- ...regional equivalent for Canada 3 - 5 years previous experience in pharmacovigilance and/or medical monitoring is required. Previous CRO experience is highly desirable, but individuals with relevant experience as a Patient Safety/Drug Safety Physician within Industry...SuggestedInternshipWork at officeLocal areaRemote workWork from homeFlexible hours
$60k - $90k
...validation in the pharmaceutical or medical device industries. Ideal candidates will have strong communication skills and experience with computerized system development. This position offers a competitive salary between $60,000 and $90,000 annually. #J-18808-Ljbffr Katalyst CROSuggested- ...and a passion for digital commerce and brand-led storytelling. Responsibilities also include cross-functional collaboration, leading CRO efforts, and ensuring a consistent, premium customer experience across devices and geographies. Hiring Manager Title CEO Travel...SuggestedWork at office
- ...medicine. Will work closely with project managers (central and/or specialty labs) and lend expertise to clinical trial management (CTM) and CRO to ensure samples are collected per protocol and assist with resolving any sample related issues or queries. Additional...Suggested
- ...epidemiology, biostatistics, statistics, bioinformatics, economics) and 5+ years of experience conducting RWE analytics for pharma industry, CRO, or academic institution Intermediate to expert level proficiency in SQL is a must. In addition, SAS or R proficiency is required...Suggested
$118k - $130k
...of the above education requirement, candidates with a minimum of 3 years relevant clinical research experience in pharmaceutical or CRO industries will be considered. Thorough knowledge of regulatory requirements including a basic understanding of regulatory requirements...SuggestedRemote jobFull timePart timeWork at officeLocal areaFlexible hoursNight shift- ...programming preferred. Education Bachelor’s or master’s degree. Experience 6+ years of clinical research experience in academic, CRO, or pharmaceutical/biotech settings, with knowledge of clinical trials and clinical databases. EEO Disclaimer Parexel is an equal opportunity...Suggested
- ...-ready at all times Consent version control accuracy at 100% with timely re-consents Query turnaround ≤2 business days for sponsor/CRO requests Reliable support of 6-10 patient visits per 8.5-hour day without documentation backlog Onboarding We will help you do a great...SuggestedFull timeWork at officeMonday to FridayWeekend work
$205k - $341.6k
...strategy and oversight for vendor selection and management within a clinical program(s) Manages the Clinical Research Organization (CRO) and vendor(s) as it relates to clinical program level deliverables and relationship with key CRO (functional and project) and vendor...SuggestedRemote workFlexible hours3 days per week- ...such as nursing, pharmacy, or health science or equivalent relevant experience At least 5 years of relevant pharmaceutical, site, or CRO Regulatory experience About CTI CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract...Contract workWork at officeLocal areaWork from home
$260k - $330k
...clinical studies, ensuring medical validity of each primary endpoint and study subject safety, and discussing early medical issues with the CRO Medical Monitor. Collaborate on clinical trial data for regulatory documents (e.g., CSRs, INDs, annual reports, NDAs, MAAs),...Immediate start$132k - $152k
...Contribute to the development of monitoring strategies and plans, ensuring effective execution through oversight of in-house and CRO monitoring activities, including the implementation of risk-based monitoring approaches Proactively identify, assess, and mitigate...Full timeTemporary workLocal areaRemote workFlexible hoursProject Leadership - Biotech (clinical trials) -Neurology/Psych/Rare Disease - Home Based - (Fu[...]
...: advanced degree preferred, along with at minimum, 2+ years' experience leading Global Clinal Trials in Project Management within a CRO (preferred), Biotech or Pharma company. These positions also require experience in project scheduling, managing resources and budgets...Remote workWork from home- ...preferably with advanced certification (eg, CRP, PMP) in a related field such as clinical project management At least 7 years experience in a CRO environment At least 5 years managing global, site-based, Phase IV prospective studies from start to finish in a CRO At least 5 years...Contract workWork from home
- ...PhD, or master’s Level advanced scientific degree Minimum 10 years of regulatory affairs and/or clinical development experience in CRO, biotech, or pharmaceutical environments Demonstrated experience serving as a regulatory strategy lead across multiple programs...Remote jobFull timeContract workWork at officeWork from home
$24 - $27 per hour
...conversion and re-engagement campaigns. This role requires a dedicated focus on top-of-funnel management, conversion rate optimization (CRO), and delivering the highest standard of sales communication and training to the Front Desk team. Success is measured strictly by...Hourly payPermanent employmentFull timeTemporary workSummer holidaySeasonal workWork at officeLocal areaMonday to FridayFlexible hoursWeekend work- ...experience or an equivalent combination of education and relevant work experience At least 6 years of clinical research experience (CRO CRA or Research Manager, Site Research Manager, Central Clinical Research Laboratory Manager) or possesses transferrable skills and...Full timeContract workWork experience placementWork from homeRelocation package
$99k - $180k
...is a plus ~ Late Phase Oncology, ideally women's health solid tumor is a plus ~ Strong project management experience and Vendor/CRO oversight ~ Demonstrated collaboration and superb communication skills, both written and oral (proficiency in English required)....Remote workPAREXEL
Frankfort, KY3 days ago- ...Education US Board certified in Ophthalmology Experience as a Physician in Industry or as a clinical trial investigator is required Previous CRO experience is required Medically qualified in an acknowledged medical school with completion of at least basic training in clinical...InternshipRemote workFlexible hours
PAREXEL
Frankfort, KY4 days ago - ..., GAMP 4. ~ Ability to create infrastructure/data flow diagrams. ~ Detail-oriented with strong communication and stakeholder engagement skills. ~6-9 years relevant validation experience (pharma / biotech / CRO ). ~ Familiarity with CSA Principles....
Katalyst Healthcares and Life Sciences
Newport, KY4 days ago - ...online customer experience, and maximize lifetime value. You will oversee the entire digital storefront, including site merchandising, CRO initiatives, subscription programs, and product launches, while aligning cross‑functional teams to execute high‑impact strategies....Remote workFlexible hours
Jobgether
Frankfort, KY4 days ago $120k - $170k
...ABOUT ALIMENTIV Alimentiv is a global CRO with a singular focus: advancing therapies for patients with gastrointestinal diseases. GI is our WHY and for more than 30 years that purpose has driven our scientific rigour, operational excellence, and deep therapeutic expertise...Remote workMedium
London, KY4 days ago- ...About CTI CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research...Full timeContract workRemote workWork from home
Consulting, Inc.
Covington, KY4 days ago - ...ensuring on-time delivery within budget. Ideal candidates will have a minimum of 2 years' experience in Project Management within a CRO, Biotech, or Pharma company and possess strong problem-solving skills along with a detail-oriented mindset. This role supports Biotech...Remote work
PAREXEL
Frankfort, KY18 hours ago
