Nebraska Clinical Trial Manager Jobs

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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 Tue 14th May
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...
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Posted Wed 8th May
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...
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Posted Thu 16th May
Manager, Trial Master FileIcon(Philadelphia, Pennsylvania)
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. The Manager of the Trial Master Owner Group will serve as the Functional Lead for Clinical Operations with responsibility for the delivery of inspection ready Trial Master Files (TMF), ensu...
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Posted Fri 3rd May
Trial Safety Surveillance ManagerIvory Systems(Northern, New Jersey)
We are looking for a Trials Safety Surveillance Manager either as a salaried employee with fully paid benefits, vacation or as an hourly employee. Responsible for • Identifying and assisting in the management of safety concerns within trials • Assisting Medical Affairs trials teams in implementing, executing and concluding trials • Assisting lead safety MDs in their evaluation of products’ safety ...
Full job description at Monster
Posted Thu 9th May
Trial Master Files ManagerRandstad Pharma(Boston, Massachusetts)
Job Title: TMF Manager Position Description This position is responsible for management of Clinical and other sections of the Trail Master Files (TMF), utilizing records management best practices and appropriate technologies. The individual will provide leadership and expertise in records management and archiving support for clinical research work. Including the completeness, safekeeping and acces...
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Posted Tue 14th May
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
Project Manager, Clinical Supply Chain Optimization (193-050)BioClinica, Inc.(Southeast/New London, Connecticut)
BioClinica, Inc. is currently recruiting for the position of Project Manager, Clinical Supply Chain Optimization. This position can be located in either the New London, CT, Sherborn, MA or Audubon, PA office. BioClinica Optimizer is the only clinical trial supply forecasting software that accurately eliminates unnecessary overage, minimizes drug waste and reduces trial costs by defining the supply...
Full job description at Monster
Posted Fri 22nd March
Sales ManagerGpac(Lincoln, Nebraska)
Are you looking for an exciting challenge? We need an experienced sales person with strong technical understanding of commercial dust collection systems to join our team. Our company is rapidly growing, financially stable and we offer a top of the line product. We serve multiple industries like grain, milling and wood. We need someone who can walk in and size up a project for a 1 million bushel gr...
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Posted Fri 22nd March
Clinical Project ManagerJoule Clinical(Boston, Massachusetts)
The Clinical Project Manager is responsible for independently managing multiple clinical trials of moderate complexity or managing a broader range of activities on large multi-center studies. The Clinical Project Manager is expected to address site and vendor related issues, with assistance as needed. Specific responsibilities include the clinical trial management of timelines, budgets, resources,...
Full job description at Monster
Posted Mon 25th March
Senior Manager Clinical Supplies - New JerseyMRINetwork(Philadelphia, Pennsylvania)
Senior Manager Clinical Supplies - New Jersey My client is a well-funded global biotech company with multiple programs in late stage clinical trials. They were recently awarded over $50 Million in funding. They have retained Klein Hersh to bring on a Senior Manager Clinical Supplies. This is a key role within the organization, reporting into the Vice President. Additionally, the Senior Manager Cli...
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Posted Wed 3rd April
Senior Clinical Project Manager/Study Manager – Emerging Pharma (Biologics/Top Dollar)Frankel Staffing Partners(Raleigh/Durham-RTP, North Carolina)
Our client, an RTP-based life sciences company undergoing tremendous growth, is actively recruiting for a proactive, skilled, knowledgeable and focused Clinical Research professional to assume key role on its Clinical team. The company is thriving, new products are being launched and the pipeline is rich. Identifying an outstanding performer to lead global programs currently underway is a top prio...
Full job description at Monster
Posted Wed 17th April
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 Data ManagerRandstad Pharma(San Francisco, California)
Job Title: Clinical Data Manager Position Description The Clinical Data Manager (CDM) is responsible for the creation, updating, maintenance and validation of clinical study databases and for the provision of computerized reports of these data. The CDM is a key member of the clinical project team and will prioritize work in line with departmental and organizational management decisions. The respon...
Full job description at Monster
Posted Tue 23rd April
Clinical Trial LeaderRandstad Pharma(Boston, Massachusetts)
Job Title: Clinical Trial Leader Position 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. Position Responsibilities Lead the clinical protocol development process in coll...
Full job description at Monster
Posted Fri 26th April
Clinical Trial HeadRandstad Pharma(Boston, Massachusetts)
Job Title: Clinical Trial Head Position 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. Position Responsibilities Lead the clinical protocol development process in collab...
Full job description at Monster
Posted Fri 26th 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
Sr. Clinical Study ManagerPurdue Pharma L.P.(Stamford, Connecticut)
The Sr. Clinical Study Manager (Sr. CSM) organizes and facilitates the overall planning, coordination, tracking and general performance of clinical studies that support the Clinical Development Plan. The Sr. CSM is responsible for ensuring clinical study quality/consistency of performance and in conjunction with the Clinical Leader and all other Team members is responsible for overall timeline adh...
Full job description at Monster
Posted Thu 2nd May

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