Remote Market Research Participant Up to $90/Session No Experience Required Occupons QuebecRemote Market Research Participant Up to $90/Session No Experience RequiredDavidview, CONNECTICUTRemoteYou will complete a short screening form so our system can match you with relevant consumer research opportunities within our national insights program. All tasks are conducted online and can be completed outside traditional business hours.
FSP Clinical Research Associate 2 Fortrea IncFSP Clinical Research Associate 2CTRemote$100,000–$112,000 / yearResponsibilities: Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.
NewSenior Clinical Study Manager - Remote Penfield Search PartnersSenior Clinical Study Manager - RemoteFairfield, CTRemoteClinical Study Manager role is responsible for managing the overall clinical operations of pre-clinical and clinical diagnostic trials, including study planning, budgeting, resource management, and, when applicable, oversight of contract research organizations (CROs). Develop and maintain effective communication across functions, including Executive/Leadership, Research & Development, Medical Affairs, Scientific Affairs, Regulatory Affairs, Finance, and Commercial teams.
Data Scientist - Clinical Analytics (Remote) Penfield Search PartnersData Scientist - Clinical Analytics (Remote)Fairfield, CTRemoteThe ideal candidate combines strong programming and technical development skills with an understanding of clinical studies and the ability to build practical solutions that improve how teams access, analyze, visualize, and work with clinical data. Strong cross-functional communication skills with the ability to work effectively across Biostatistics, Statistical Programming, Data Management, and other clinical functions.
Clinical Database Programmer - Remote Penfield Search PartnersClinical Database Programmer - RemoteFairfield, CTRemoteThe ideal candidate will have extensive hands-on Medidata Rave programming experience and the ability to independently build and maintain clinical databases while also supporting traditional clinical data management activities. Develop, review, execute, and document database testing and User Acceptance Testing (UAT) to ensure database functionality and data quality prior to production release and following database amendments.
Biostatistician - Early Phase (Remote) Penfield Search PartnersBiostatistician - Early Phase (Remote)Fairfield, CTRemoteThe Biostatistician applies statistical expertise across clinical research projects, independently supporting or leading studies, performing statistical analyses, and delivering high-quality statistical documents and outputs in support of sponsors' clinical development programs. Experience supporting Phase 1 and early clinical development studies is strongly preferred, including familiarity with early-phase study designs, safety and tolerability endpoints, pharmacokinetic/pharmacodynamic (PK/PD) data, dose escalation, and exploratory analyses.
Executive Medical Director, Neurology, Clinical Development (Remote) Penfield Search PartnersExecutive Medical Director, Neurology, Clinical Development (Remote)Fairfield, CTRemoteProvide medical and clinical expertise to internal stakeholders, including Research & Development, Commercial, Marketing, Manufacturing, Market Access, Patient Services, Regulatory Affairs, and Legal, as well as external stakeholders such as healthcare professionals, advocacy groups, and data monitoring committees. This highly visible leadership role will drive clinical programs from early development through registration, provide medical leadership across cross-functional teams, and help shape the future of our neurology gene therapy portfolio.
Senior Clinical Data Manager (Remote - US) MMSSenior Clinical Data Manager (Remote - US)Bridgeport, CTRemoteProvides oversight and resolves all issues in data management study processing activities including CRF tracking and data entry, integration of external electronic data (e.g., lab data) with clinical database, data validation and review, query processing and resolution, adverse event and medication coding, SAE reconciliation, database lock and database QC audits. Oversees and develops data management study documentation including Case Report Forms, CRF Completion Guidelines, Database Design via annotated CRFs, Validation specifications (edit checks), and Data Management Plan.
NewStudy Site Engagement Lead (Remote) Boehringer Ingelheim International GmbHStudy Site Engagement Lead (Remote)Ridgefield, CTRemote$165,600–$248,400 / yearIdentify and maintain operational relationships with research investigators & sites in alignment with Medicine strategic needs: Identify clinical trial investigators, sites, & relationships to bring to trial teams to fulfill pipeline needs (e.g., access to a certain patient population). The role is to actively engage with investigational sites in all stages of clinical trial development activities from protocol development through to study completion, and across multiple programs, thus contributing to accelerated and more efficient clinical development of Boehringer assets through improved site performance.
(Senior) Associate Director, Principal Clinical Data Scientist -Early Oncology ExpMed(Remote) Boehringer Ingelheim(Senior) Associate Director, Principal Clinical Data Scientist -Early Oncology ExpMed(Remote)Ridgefield, CTRemote$140,000–$222,000 / yearSupport the early Oncology clinical drug research and development process by providing strategic planning and execution, including clinical trial design and all aspects of descriptive, diagnostic, predictive and prescriptive analytics of data related to clinical projects like actual trial data, registries and real-world data bases. In addition to what is listed above, you will also be responsible for the following: + Subject Matter Expert (SME) / Process Lead for designing, transforming, analyzing and reporting complex early Oncology clinical trials or projects, that represent new challenges and for which project and therapeutic knowledge is not given.
Principal Biostatistician - Medical Affairs (Remote) Penfield Search PartnersPrincipal Biostatistician - Medical Affairs (Remote)Fairfield, CTRemoteDevelop real world evidence strategies utilizing real-world data assets to design and execute RWE research projects, including the development of protocols and statistical analysis plans, in collaboration with epidemiology and RWE leadership team. The role will provide statistical guidance on clinical and lifecycle management initiatives, advise on analytical strategies, and recommend appropriate methodological approaches to support integrated evidence generation and informed decision-making.
Quality System Manager - Remote Jackson LaboratoryQuality System Manager - RemoteFarmington, CTRemoteThis position will develop and execute JAX-wide strategies to enhance process efficiency, improve risk mitigation, and oversee key quality functions, including internal and external audits, deviation reviews, CAPA facilitation, document control, and change management. About JAX: The Jackson Laboratory is an independent, nonprofit biomedical research institution with a National Cancer Institute-designated Cancer Center and nearly 3,000 employees in locations across the United States (Maine, Connecticut, California), Japan and China.
Gynecologist - IMLC License | Flexible 1099 Remote AllaraGynecologist - IMLC License | Flexible 1099 RemoteConnecticutRemoteExperience: Minimum of 2 years of consecutive clinical experience as a Gynecologist, with a focus on chronic and complex women's health conditions including PCOS, Endometriosis, Hypothyroidism, Hashimoto's, Metabolic Syndrome, Menopause, Fertility, Postpartum, PMDD, and Obesity. Trusted by over 60,000 women nationwide, Allara makes expert healthcare accessible by connecting patients with multidisciplinary care teams that have a deep understanding of hormonal, metabolic, and reproductive care.
Technical Clinical Data Manager /Data Analyst (Remote) Penfield Search PartnersTechnical Clinical Data Manager /Data Analyst (Remote)Fairfield, CTRemoteThis role will sit within a highly collaborative clinical development team and is ideal for a hands-on, analytical Clinical Data Manager who enjoys digging into the data, identifying trends or issues proactively, and developing creative solutions to improve data quality and study execution. We are partnering with a growing biotech organization seeking a Clinical Data Manager/Data Analyst to support ongoing and upcoming clinical programs across multiple therapeutic areas.
Endocrinologist - IMLC License | Flexible 1099 Remote AllaraEndocrinologist - IMLC License | Flexible 1099 RemoteConnecticutRemoteTrusted by over 60,000 women nationwide, Allara makes expert healthcare accessible by connecting patients with multidisciplinary care teams that have a deep understanding of hormonal, metabolic, and reproductive care. Allara provides ongoing support for hormonal conditions like PCOS, chronic conditions like insulin resistance, and life stages like perimenopause, helping patients see improved health outcomes .
Remote Leisure Advisor HopesglobalgetawaysRemote Leisure AdvisorFairfield, ConnecticutRemoteClient requests may include resort vacations, cruises, all-inclusive stays, family adventures, couples retreats, group trips, special celebrations, guided experiences, and international destinations. Hope's Global Getaways is a remote travel planning company powered by a full-service travel agency that specializes in destination weddings, honeymoons, cruises, family vacations, and luxury getaways.
Analyst Charge Revenue Integrity (Charge Capture Auditor) (Remote) Trinity HealthAnalyst Charge Revenue Integrity (Charge Capture Auditor) (Remote)Waterbury, CTRemote$21.52–$32.28 / hourExperience working with current medical terminology, data entry, supply chain processes, hospital and/or Medical Group practice operations; hospital and/or Physician group practice revenue cycle front-end functions such as patient registration that may impact charge related errors; and billing and regulatory guidelines related to charging and other revenue cycle processes and ability to assist clinical departments and/or physician practices with changes to their charging practices based on guidelines. May perform or provide "at elbow" guidance to clinical departmental daily reconciliation processes including ensuring supply charges are appropriate captured (may include implants), identify duplicate charges and initiate appropriate communications when there are documentation and/or charge deficiencies or charge errors.
Associate Director, Biostatistics - Remote Penfield Search PartnersAssociate Director, Biostatistics - RemoteFairfield, CTRemoteThis role involves overseeing CROs and collaborating with cross-functional teams to deliver high-quality analysis outputs and interpret results. You will be responsible for discussing and shaping the clinical development plan, study design, endpoint selection, statistical analysis plan, and regulatory submission and publication strategy to support pursuant of precision medicine.
NewMedical Writing Operations & Quality Control - Remote Penfield Search PartnersMedical Writing Operations & Quality Control - RemoteFairfield, CTRemoteSupport submission readiness and document publishing, including document completeness, consistency, formatting, version control, bookmarks, hyperlinks, tables of contents, pagination, and other final production elements. This role will partner closely with the Head of Medical Writing and QC team to ensure high-quality, compliant clinical and regulatory documents while optimizing vendor workflows and operational processes.
Senior Manager, Statistical Programming (Remote) Penfield Search PartnersSenior Manager, Statistical Programming (Remote)Fairfield, CTRemoteKey Project Responsibilities: Provide programming leadership and oversee study to compound-level programming deliverables in collaboration with the lead biostatistician and cross-functional teams. This position serves as a critical bridge between Biostatistics and Clinical Data Management (CDM), ensuring the development of CRFs and the delivery of high-quality clinical data.