Get new jobs by email
- Clinical Scientist - Immunology (Expertise in Ulcerative Colitis, Crohn’s disease and Rheumatology + Excel) - Clinical Drug Trial Exp - Must Have Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success...SuggestedContract workFlexible hours
$150k - $165k
...requirements. Document design specifications, test plans, and validation reports per regulatory requirements. Support clinical trials and post-market activities by analyzing system performance and deploying software updates. Apply AI-based techniques for code development...SuggestedFull timeEnterra Medical
Minnesota14 hours ago- ...Clinical Trial Specialist Our start-up medical device client is adding a Clinical Trial Specialist to the team. If you're looking for a role that goes beyond coordinating studies and puts you closer to the patient, the procedure, and the impactthis is it. We're partnering...Suggested
$42 per hour
...Schedule and Terms! Hiring Per Diem Registered Dietitians for Virtual Visits! EmVenio Research provides quality, in-home clinical trial visits for various Sponsors and CROs. We're the only company that hires, trains, certifies, tests, and manages our own Registered...SuggestedHourly payDaily paidReliefFlexible hours$22 - $28 per hour
Job Title Location 3601 W 76th St, Suite 300, Edina, MN, 55435, United States Base Pay $22.00 - $28.00 / Hour Employee Type Nonexempt FT Required Degree High School Manage Others No Minimum Experience 2 Years Retina Consultants of MinnesotaSuggested- ...worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive...SuggestedContract workFlexible hours
- ...customers and defining the pace of patient progress. Job Responsibilities Project Administration Creates and maintains the Trial Master File Management (TMF) Plan. Routinely reviews the TMF to ensure quality, completeness and inspection readiness Coordinates...SuggestedContract workInterim role
- ...Familiarity with regulatory submission expectations (e.g., FDA/PMDA) Ideal Profile Proven experience working in clinical trial data environments Hands-on exposure to SDTM and ADaM dataset creation or review Strong ability to translate between: Clinical...Suggested
- Minnesota Oncology is seeking a detail-oriented data entry specialist to support clinical trials across Maplewood, Woodbury, and Hudson clinics. You will input data, ensure timely submission, and uphold GCP and HIPAA standards in a collaborative setting. The role requires...Suggested
- ...expertise to other health professionals. The HealthPartners Cancer Research Center The HealthPartners Cancer Research Center offers trials to help prevent, screen for, diagnose, and treat cancer and manage the side effects of treatment and the symptoms of the disease....SuggestedFull timeLocal area
- Minnesota Oncology is seeking a data coordinator for clinical trials who will ensure accurate data entry and timely submission, collaborating with clinical staff to maintain protocol compliance and high-quality records. The role supports Maplewood, Woodbury, and Hudson...Suggested
$30 per hour
...SUMMARY ~ Conduct consumer samplings at liquor stores, bars, and restaurants to drive brand awareness, ~ product education and trial for up-and-coming and established beverage alcohol brands Collect ~ sales results and consumer and account feedback ~ Part-time...SuggestedPart timeFlexible hours$3,780 - $4,376 per month
...are currently seeking an applicant who is interested in becoming part of an experienced litigation team that has a high capacity for trials and offers an expansive opportunity for courtroom practice. Apply now to be considered for this opportunity to grow your criminal...SuggestedWork experience placementWork at office- ...close controls Define and drive the end-to-end close sequence, with clear ownership, dependencies, and monitoring Deliver trial balance, core financial statements, and close reporting outputs Subledger Accounting (SLA) & Cross-Module Coordination Design and...SuggestedLocal area
$150k - $160k
...Documenting design specifications, test plans, and validation reports in accordance with regulatory requirements. Supporting clinical trials and post-market activities by analyzing system performance and deploying software updates. Applying AI-based techniques for code...SuggestedPermanent employmentFlexible hours- ...immediate opening, qualified candidates will be considered as opportunities become available. *Looking for SME in Immunology Clinical Trials -Serves as a scientific resource for RWLP management, Company senior management, and other Functions within Company providing...Contract workInterim roleImmediate startRemote workFlexible hours
- ...Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site is aware of the requirement of archiving essential documents in...Contract workInterim roleLocal areaImmediate startRemote workFlexible hours
$75.2k - $112.8k
...coordination support. Nice To Have Experience supporting multi-site or global clinical studies. Experience with electronic trial master file (eTMF), CTMS, EDC, and document management systems (e.g., Medidata Rave, Veeva Vault, Cornerstone OnDemand). Strong understanding...Full timeH1bWork at officeLocal areaImmediate startFlexible hours$47k - $79.9k
...customers and defining the pace of patient progress. Job Responsibilities Responsible for planning, coordination and conduct of trial activities according to ICH-GCP. Assures the seamless conduct of trials within the defined timelines in close coordination and...Contract workLocal areaRemote workFlexible hours$130k - $160k
...including design specifications, test plans, and validation reports, in accordance with regulatory requirements. Support clinical trials and post-market surveillance by analyzing device performance and implementing firmware updates as needed. Qualifications ~...Full timeWork at office$25.2 per hour
...data ~ Previous experience with IRB ~ Prior experience managing quantitative data ~2 years Minimum of experience in clinical trial conduct preferred. ~ Training and knowledge of clinical research activities and regulatory requirements preferred. ~ Working understanding...Hourly payFull timeMonday to Friday- ...hours using systems such as Copitrak or Equitrak. ~ Assist with closing binders, depositions, court system processes, and offsite trial support (scheduling equipment, labor, and supplies). ~ Function as a document specialist while delivering professional support to...Contract workWork at officeShift work
$120k - $135k
...innovative therapies to patients worldwide? We are seeking experienced Clinical Project Managers with strong global oncology clinical trial experience to join a high-performing sponsor-dedicated team supporting a diverse portfolio of oncology studies across multiple...Contract workWork at officeImmediate startRemote workWorldwideFlexible hours$130k - $160k
...Create and maintain detailed documentation including design specifications, validation reports, and test plans Support clinical trials and post-market activities by analyzing device performance and implementing firmware updates Contribute to continuous improvement...Permanent employmentFlexible hours$102.1k
..., ranking No. 15 on the Top 100 list, reflecting the culture our employees experience every day. The Manager, Global Clinical Trial Operations provides leadership to assigned trial operations team members in support of global, cross-divisional clinical trials and...Hourly payWork at officeLocal areaRelocationRelocation packageShift work3 days per week- ...Description Apply Here: & TrackId=ZipRecruiter We are seeking multiple outgoing, patient focused individuals to work as Clinical Trials Research Assistant at our Retina Consultants of Minnesota Edina, MN clinic. Responsibilities for an Clinical Trials Research...Temporary workFlexible hours
$79.8k - $139.6k
...Contracts Manager , you’ll serve as a strategic expert responsible for developing, negotiating, and managing US site budgets and clinical trial agreements. You’ll collaborate closely with internal teams, external stakeholders, and major academic institutions to craft robust...Contract workImmediate startRemote workFlexible hours$29.77 - $32.83 per hour
...reviewing, filing, and tracking legal documents. Manage criminal and civil case files, deadlines, discovery, and court calendars. Prepare trial and hearing materials and assist attorneys during proceedings. Organize, distribute, track, and redact discovery materials across...Work experience placementWork at officeMinnehaha County
Minnesota5 days ago$100k - $300k
...Minnesota. This position will involve record review, legal research, legal writing, negotiations, discovery, depositions, hearings, trial, and other work advocating for injured clients in the Midwest. *Responsibilities:* * Manage a personal injury caseload including...Full timeTemporary workWork at officeMonday to FridayShift workWeekend workDay shiftAfternoon shiftNicolet Law
Minnesota4 days ago$114k - $210.9k
...Based Candidates Are you a senior clinical operations professional who knows how to independently lead complex global clinical trials from start-up through closeout — while still staying deeply connected to the operational details that drive execution success?...Contract workRemote workWork from homeFlexible hours2 days per week3 days per week
