Alabama Clinical Trial Manager Jobs

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  • Esperion Therapeutics Clinical Trial ManagerEsperion Therapeutics, Inc.(Ann Arbor, Michigan)

    PrincipalResponsibilities: · Operationally manages one or more clinical trials · Clinical trial creation, management and execution activities and progress in accordance with Good Clinical Practice (GCP) · Ensure compliance of clinical trials with local regulatory requirements · Assist in establishing study timelines and critical milestones · Evaluates CROs and vendors (e.g., patient recruitment, c...
    Full job description at Monster

    Posted Sat 25th May

  • Sr. Clinical Trial ManagerSRG Woolf Group(Boston, Massachusetts)

    A biopharmaceutical company located just outside of Boston, MA is seeking a Sr. Clinical Trial Manager (Sr. CTM) to join their team. Our client offers a very competitive salary and comprehensive benefits! This is an office based, permanent position. PURPOSE OF POSITION: The Sr. CTM will lead the forecasting, planning and management of the clinical operational plans. The Sr. CTM will be responsible...
    Full job description at Monster

    Posted Wed 29th May

  • Clinical Trial ManagerIcon(Raleigh/Durham-RTP, North Carolina)

    Clinical Trial Manager with ICON Late Phase & Outcomes Research Location – Raleigh/Durham, NC This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Our Clinical Trial Managers act as the Functional Lead from Clinical Operations with responsibi...
    Full job description at Monster

    Posted Thu 30th May

  • Clinical Trial Manager/Senior Clinical Trial ManagerCelldex Therapeutics(New Haven, Connecticut)

    Summary of Position: The Clinical Trial Manager / Senior Clinical Trial Manager works closely with internal team members and vendors to ensure that assigned clinical trials are conducted per protocol, in a timely fashion and in a manner compliant with SOPs, ICH/GCP/regulatory guidelines, company goals and established study budgets. Individual responsibilities include: • Comprehensive oversight of ...
    Full job description at Monster

    Posted Mon 3rd June

  • Clinical Trial ManagerNetsource, Inc.(Silicon Valley/San Jose, California)

    Please note this is a FULL TIME PERMANENT position. Skills:Clinical Trial Manager experience, CRA experience, Pharma Industry, FDA Regulations experience Leads activities associated with LOI evaluation and protocol review. Coordinates the review and communication of PCYC comments on IST and CTEP studies. In collaboration with the Director, oversees IST and CTEP team members, including oversight of...
    Full job description at Monster

    Posted 3 days ago

  • Statistician&SAS(remote),LSH–Oracle Clinical,Medical Writer,Clinical Data Manager,Biomarker Trial HeTechData(Northern, New Jersey)

    TechData is hiring Biostatistician (some can telecommute), SAS Programmer (Some can be telecommute), Sr. Clinical data manager, Sr. Medical Writer,Life Sciences Hub (LSH) Consultant and Oracle Clinical for Global Librarian/Modeler, Biomarker Trial head for our pharmaceutical clients in Northern NJ. Please see below requirements and send your inquiry and resume to: dan.chen@techdataservice.com or r...
    Full job description at Monster

    Posted Yesterday

  • Project Manager - Pharmaceutical Industry, Clinical Trial SystemCyberCoders(Boise, Idaho)

    CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Project Manager Boise, ID; Irvine, CA Unspecified Posted 6/19/2013 Stephanie Eldred is recruiting for this position. Email your resume to Stephanie Apply Job Details We have a fantastic Project Manager opening in Boise, ID. We are growing our Operations Teams and we need a Project Manager with a Pharmaceutical and/...
    Full job description at Monster

    Posted Yesterday

  • Assistant Clinical Trial ManagerCelldex Therapeutics(New Haven, Connecticut)

    Position Responsibilities: Clinical Trial Oversight • Comprehensive oversight of operational aspects of assigned clinical trials. The assigned trials would generally be less complex and domestic trials. Responsibilities would include the preparation and/or review/approval of study-related documents (e.g., Laboratory Manual, Monitoring Plan, Patient Diary, Clinical Site Procedures Manual, Pharmacy ...
    Full job description at Monster

    Posted Thu 13th June

  • Sr. Clinical Research Associate/Clinical Trial ManagerNetsource, Inc.(Silicon Valley/San Jose, California)

    Please note this is a FULL TIME PERMANENT position. Skills:Clinical Trial experience, Clinical Studies, BS/BA -RN Degree, Global Trial Preferred, FDA Regulations Key Accountabilities/Core Job Responsibilities: Lead multifunctional team through clinical studies activities that meet ICH/GCP and SOP requirements Develop clinical trial protocol synopsis, protocols, amendments and informed consent docu...
    Full job description at Monster

    Posted 2 days ago

  • Clinical Trial Supply Operations – Direct Hire/RTP PharmaFrankel Staffing Partners(Raleigh/Durham-RTP, North Carolina)

    Our client, an RTP-based pharmaceutical company in high growth mode, is actively recruiting for a very sharp and capable Clinical Supplies professional to drive all Clinical Supply operations. This is a great “foot in the door” opportunity with a company that is developing compounds that are highly anticipated in the medical community-worldwide. Seek a skilled, self-directed and knowledgeable cand...
    Full job description at Monster

    Posted Wed 8th May

  • Lead Clinical Trial CoordinatorShire(San Diego, California)

    Primary Duties Responsible for assisting/providing support to members of the Global Clinical Operations project team and other cross-functional customers in the planning and implementation of clinical development investigational studies for one or several studies and/or programs at the global level. Responsible for assisting and providing support to Head, Clinical Operations for ad-hoc stand-alone...
    Full job description at Monster

    Posted Fri 14th June

  • Clinical Trial Administrator/Document SpecialistCelldex Therapeutics(New Haven, Connecticut)

    Clinical Trial Administrator/Document Specialist This position is based in the CT office. The position will be responsible for the overall provision of competent, professional administrative support and assistance to the Celldex Clinical Department in the implementation and management of clinical trials. Assignments will include routine clerical tasks, administrative support functions and clinical...
    Full job description at Monster

    Posted Sat 15th June

  • Start-Up Clinical Trial Scientist JobYoh(Northern, New Jersey)

    Yoh has a long term contract opportunity for a Start-Up Clinical Trial Scientist to join our client located inEast Hanover, NJ. Job Responsibilities: - Process, collect and track all the operational aspect of the study start up program for Rare Diseases for USCDMA including, but not limited to, TPS and compassionate use - Responsible for execution of confidentiality agreements, review and processi...
    Full job description at Monster

    Posted Fri 7th June

  • Trial Communications ManagerTrialNetworks(Boston, Massachusetts)

    We’re looking for an energetic, outgoing and detail oriented individual with a passion for improving how information is communicated in clinical trials. Acting as an extension of our client’s clinical trial operations group, you will use our novel technology platform to create and manage communication to clinical trial sites, motivating study team members to recruit and retain trial participants. ...
    Full job description at Monster

    Posted Mon 6th May

  • Clinical Trial Associate(Northern, New Jersey)

    We have several positions and are eagerly reviewing new candidates. Please submit your resume if you feel you meet the necessary requirements below: The Clinical Trials Associate (CTA) is involved in the conduct of the study and interfaces with the Study Manager and the Study Team. Requirements: BA/BS in directly-relevant discipline or equivalent experience required At least 2 years experience as ...
    Full job description at Monster

    Posted Thu 6th June

  • Clinical Trial Leader II 90616InVentiv(Boston, Massachusetts)

    JOB DESCRIPTION: Accountable for all aspects of assigned OTM clinical trials (Phase I/II) including leading Clinical Trial Team(s) (CTT). Number of clinical trials depends on the workload and complexity of the individual trials. Responsible for program level activities as assigned. Major Accountabilities Lead the clinical protocol development process in collaboration with the Clinical Program Lead...
    Full job description at Monster

    Posted Tue 23rd April

  • Clinical Project ManagerLEO Pharma Inc.(Northern, New Jersey)

    LEO Pharma Inc. is a leading global pharmaceutical company specializing in dermatology and critical care. For 100+ years, our products have improved the quality of millions of people's lives around the world. Headquartered in Denmark, we have 4500 employees in 50+ countries and our products are sold in more than 100 countries. To realize our vision of becoming the world’s leading specialty pharmac...
    Full job description at Monster

    Posted Mon 29th April

  • Clinical Data ManagerClinicalRM(Frederick/Hagerstown, Maryland)

    Growing and well-respected biomedical (clinical, basic and applied) research firm has openings at USAMMDA. If you are passionate about research, and are looking for a firm that shares your passion, and provides competitive salaries with a strong benefits package, join the ClinicalRM team. We are currently seeking a Clinical Data Manager for the Frederick, Maryland area. RESPONSIBILITIES: Assist Se...
    Full job description at Monster

    Posted Tue 30th April

  • Clinical Data ManagerThe EMMES Corporation(Montgomery County, Maryland)

    The EMMES Corporation, organized in 1977, is a privately owned Contract Research Organization (CRO) located in Rockville, Maryland. EMMES is dedicated to providing statistical and epidemiological expertise, computer systems development, data management, study monitoring, regulatory guidance, and overall operational support to clients engaged in clinical and biomedical research. EMMES is seeking a ...
    Full job description at Monster

    Posted Wed 1st May

  • Clinical Research Site ManagerBayview Research Group, LLC(Los Angeles, California)

    Clinical Research Site Manager A rapidly growing clinical research site management organization is seeking a Clinical Research Manager or ahighly experienced Senior Clinical Research Coordinator with excellent communication skills, proven management abilities, and an established history of successful trial recruitment and retention. The ideal candidate should be able to successfully execute and co...
    Full job description at Monster

    Posted Mon 6th May

Alabama Job Search Tip

The Alabama Department of Industrial Relations ranks Healthcare Support as the fastest growing field in Alabama. That's good news for those looking for work as Medical Assistants, Home Health Aids and Medical Records and Health Information Technicians. Those without medical expertise would do well to apply with the University of Alabama. With the exception of governmental agencies, the University of Alabama at Birmingham is Alabama's largest employer with over 15,000 employees.

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