Contract Clinical Trial Manager Position Description: Functions as the clinical study team leader to plan, organize, and coordinate all operational aspects of a clinical study from protocol development through database lock. Ensures timely conduct of clinical studies according to protocols, Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), and all applicable regulations governing the conduct of clinical trials. Job Responsibilities (Key Responsibilities): -Responsible for the preparation and finalization of project and st...

Clinical Research Associate (In-House) The Clinical Research Associate in collaboration with the Clinical Trial Manager, contributes to the operational execution of clinical studies to ensure delivery on time, within budget, and of high quality in compliance with ICH/GCP, Regulatory Authorities’ regulations/guidelines, and applicable SOPs/WPs. Responsibilities may include participation on one or more cross-functional study team(s) and/or performance and quality oversight of one or more Contract Research Organization (CRO) teams and vendors. Proj...

Clinical Research Program Manager The Company: -We are representing one of the world’s leading medical technology companies that is driven to make healthcare better. The Company offers a diverse array of innovative medical technologies, including reconstructive, medical and surgical, and neurotechnology and spine products to help people lead more active and more satisfying lives. Their products and services are available in over 100 countries. Job Description: -Responsible and accountable for several concurrent global clinical studies as p...

Lead Clinical Research Associate The Company: -We are representing one of the world’s leading medical technology companies that is driven to make healthcare better. The Company offers a diverse array of innovative medical technologies, including reconstructive, medical and surgical, and neurotechnology and spine products to help people lead more active and more satisfying lives. Their products and services are available in over 100 countries. Job Description: -Monitors and/or supervises the monitoring activities of assigned clinical trials...

Senior Clinical Research Associate Job Description / Information: -The Senior Clinical Research Associate (Sr. CRA) independently supports planning, preparation, execution, control/monitoring and closeout of clinical trials. The Sr. CRA establishes cross-functional and KOL relationships and demonstrates the ability to independently handle clinical trials. Monitors and/or supervises the monitoring activities of assigned clinical trials to ensure data integrity and adherence to Federal regulations, company policies, and any other applicable proced...

Senior Clinical Operations Lead (Director Level Role) SUMMARY: -Solves complex problems based on sophisticated analytical thought and complex judgment. -Interprets internal and external business challenges and recommends best practices to improve products, processes and services. -Is recognized as an expert within the discipline and beyond with a limited number of peers within the same technical area in the business. -Serves as best practice resource within own discipline or as technical expert on cross-functional teams or projects. -Has in-...

Principal Clinical Trial Lead (AD Level Role) KEY ACCOUNTABILITIES -Implements, conducts or monitors on-site clinical trials. -Takes responsibility for on-site operations of clinical trials, including documentation strategies, implementation of clinical trials protocols, standard operating procedures (SOPs) and case report forms (CRFs). May also help define or improve these but main emphasis will be on implementation. Conduct and be responsible for clinical studies in one or more therapeutic areas. -Leads own team of professional staff to iden...

Sr. Clinical Trial Lead The Senior Clinical Trial Lead implements, conducts or monitors on-site clinical trials. Takes responsibility for on-site operations of clinical trials, including documentation strategies, implementation of clinical trials protocols, standard operating procedures (SOPs) and case report forms (CRFs). May also help define or improve these but main emphasis will be on implementation. Conduct and be responsible for clinical studies in one or more therapeutic areas. KEY ACCOUNTABILITIES -Works effectively in a mixed environ...

Clinical Research Coordinator -BS Degree preferred -Prior coordinator experience is essential -Phase I - III experience is key -Open to all therapeutic expertise ***More detailed description can be provided upon interest!***

Clinical Research Associate -Responsible for the management of designated clinical trials including investigator selection, analysis of potential patient recruitment, preparation of trial related documentation (protocols, Case report forms, investigators brochures, consent documents, letters of agreement, confidentiality agreements), organizing Ethics committee submissions with follow through to ensure successful outcome. -Organize investigator’s start-up meeting and study site initiation meetings. -Coordinate the movement of laboratory samples a...

 Member of Study Management Team (SMT), responsible for attending study team meetings and report status of study-specific vendor/consultant contracts.  Act as the primary contact with vendors for negotiation of the scope of work, study assumptions and budgets including generation of Work Orders.  Conduct budget analysis, to include Fair Market Value (FMV) assessment, contract negotiations and execution for vendors supporting a clinical trial.  Work closely with Leader, Clinical Vendor Management, Clinical Operations team members and other rele...

Hiring full time (remote) Project Manager To save us both time, let's get the set the minimum requirements out of the way. To be considered you must have: -BS/BA in health-related field required. -Completing global research studies from initiation to submission -Minimum of 8 years of experience and or demonstrated aptitude for project management work. -Minimum of 8 years of medication, clinical, or research related study or instruction. -Experience working in CRO industry. -Working knowledge of EDC studies. -Current live or able to relocat...

Purpose/Objective of the job: To perform protocol level clinical data review and cleaning activities to support clinical trials and maintain protocol data quality Key Responsibilities and Major Duties: • Responsible for clinical data listing review at protocol level to ensure data submitted by investigative sites is of high quality and completed within predefined study timelines. • Applies clinical and scientific knowledge to prioritize the clinical data review and cleaning. • Demonstrates an understanding of the indication studied and the over...

Responsibilities • Manages and tracks investigational product (IP) inventory; advises supply management team of potential shortages and makes recommendations for resupply activities based on usage trends. • Initiates IP shipment orders according to supply plans or as requested by Clinical Trial Management team; tracks orders through receipt at investigator study sites; communicates with distribution vendors to ensure timely and compliant shipment and delivery to investigator sites. • Reviews and evaluates temperature excursion data and communica...

Responsible for managing data management teams, studies and programs of studies under the general direction of Sr. Project Manager or the Director of Data Management. • Work with Clinical Operations, CDMS, Biostatistics, CDS, ITG, Medical Writing, Regulatory Affairs and Quality Assurance to ensure that data collected during trials are managed according to corporate standards and meet regulatory guide lines for data integrity.

Job Overview: The Project Manager fulfills the requirements of managing clinical trials (at the country or regional level, typically) to ensure timely delivery of project required objectives and timelines within the scope of the client agreements for assigned projects and the project budget. In doing so, the Project Manager is responsible for the cross-functional team’s compliance with the project Standard Operating Procedures (SOPs), Good Clinical Practice (GCP)/ International Conference on Harmonization (ICH) guidelines and other applicab...

Our client is currently hiring! Join a terrific group of people, dedicated to curing cancer! Home based CRA opportunities with a successful oncology clinical research organization. Must have early phase Oncology monitoring experience. Travel of up to 70-75% Comprehensive compensation packages

Our client is currently hiring! MID WEST, WEST COAST and EAST COAST positions available. Home based CRA opportunities with a successful, global CRO. Regionalized, lower travel. Excellent Compensation and sign on bonus currently available. Please email for details!

Summary: Responsible for the development and analysis of contractual relationships including investigator grants including but not limited to drafting, negotiating, and finalizing agreements related to clinical trials. Provide support to the clinical team in the pricing, planning, execution and control of grants and contracts. Principal Responsibilities: Responsible for analyzing contract requests/needs from operating companies and translating into appropriate contracts/budgets for company sponsored and investigator initiated clinical tr...

Job Title: Clinical Research Associate Experience: 3+ years Therapeutic areas:Oncology Location: Canada Roles & Responsibilities of the position PRINCIPAL RESPONSIBILITIES: - Participates in site feasibility and/or pre-trial site assessment visits, providing recommendation from local area about site/investigator selection in collaboration with the trial team - Acts as primary local company contact for assigned sites for specific trials. - Attends/participates in investigator meetings as needed. - Responsible for executing activities...

Multiple Home Based Regional Clinical Research Associate positions available for individuals who live in or are located within a commutable distance to a major city. Opportunities available located in the following areas: Los Angeles and San Francisco, CA; North East Region (NY, NJ, PA, DC-MD, MA area); Chicago, IL and the Pacific North West. Qualified candidates must demonstrate a minimum of 3 years CRO or Pharmaceutical company clinical research on-site monitoring experience. Individuals with experience monitoring Oncology; Neuroscience, Cardiovasc...