Sr. Clinical Studies Coordinator

Job Title: Sr. Clinical Studies Coordinator Duration: 6+ month contract, intent to hire Location: Onsite- Houston, TX The Senior Coordinator, Clinical Studies is responsible for the day-to-day management and oversight of protocol compliance, patient care, and coordination of clinical trials. This role includes collaborating with the principal investigator to...

Job Title: Sr. Clinical Studies Coordinator Duration: 6+ month contract, intent to hire Location: Onsite- Houston, TX The Senior Coordinator, Clinical Studies is responsible for the day-to-day management and oversight of protocol compliance, patient care, and coordination of clinical trials. This role includes collaborating with the principal investigator to...

The primary purpose of the Senior Coordinator, Clinical Studies is to provide day-to-day management and oversight of protocol compliance, patient care, and issues related to the coordination of clinical trials. Additionally, effective operations of designated protocols include the development and resolution of issues in collaboration with the principal...

The primary purpose of the Senior Coordinator, Clinical Studies is to provide day-to-day management and oversight of protocol compliance, patient care, and issues related to the coordination of clinical trials. Additionally, effective operations of designated protocols include the development and resolution of issues in collaboration with the principal...

The primary purpose of the Senior Coordinator, Clinical Studies is to provide day-to-day management and oversight of protocol compliance, patient care, and issues related to the coordination of clinical trials. Additionally, effective operations of designated protocols include the development and resolution of issues in collaboration with the principal...

**Study Manager** A **Study Manager** is responsible to ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. In addition, ensure study enrollment meets or exceed Sponsors' expectations and company goals...

Job DescriptionJob DescriptionStudy ManagerA Study Manager is responsible to ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. In addition, ensure study enrollment meets or exceed Sponsors'...

Job DescriptionJob DescriptionStudy Start Up Manager The Study Start Up Manager is responsible for overseeing all aspects of the study start life cycle within the Program Management Organization(PMO). This role provides direct leadership to all study start up staff and contracting staff.  This role will also provide a link to senior leadership through which...

Title: Sr. Project Coordinator Location: Houston, TX Duration:Long TermRequired skills: 12 plus experience Evidence of formal Mechanical Engineering, Electrical or Instrument and Electrical education Experience in similar position Significant Experience in Equipment Maintenance is beneficial Significant direct hands on experience in maintenance and...

Responsibilities: Coordinate, evaluate, and follow patient progress while on studies maintaining knowledge of adverse events, protocol-related labs and research tests, and protocol responses. Collaborate with the multidisciplinary team as necessary to achieve the objectives of the trial. Collaborate with physicians, advanced practice...

**Clinical Data Manager - eDiary Compliance** The **Clinical Data Manager - eDiary Compliance** is responsible for overseeing the development, implementation, and maintenance of processes to ensure adherence to regulatory guidelines and protocol requirements for electronic diaries (eDiaries) utilized in clinical trials. This role involves establishing...

Job DescriptionOversee overall clinical operations related to the conduct of the trial (i.e. recruitment, informed consent procedure, visit coordination, sampling, visit scheduling, etc.)Skilled in reading, understanding, analyzing, and following clinical trial protocols and working strategically with study team to execute clinical trials.Work in...

Job DescriptionOversee overall clinical operations related to the conduct of the trial (i.e. recruitment, informed consent procedure, visit coordination, sampling, visit scheduling, etc.)Skilled in reading, understanding, analyzing, and following clinical trial protocols and working strategically with study team to execute clinical trials.Work in...

Job DescriptionJob DescriptionClinical Data Manager - eDiary ComplianceThe Clinical Data Manager - eDiary Compliance is responsible for overseeing the development, implementation, and maintenance of processes to ensure adherence to regulatory guidelines and protocol requirements for electronic diaries (eDiaries) utilized in clinical trials. This role...

Highlights:Hybrid schedule, 2 days remote per week!Lead Patient Engagement Strategy for the site!Great opportunity to make a huge impact on studiesThe CompanyOur client is a leading site network specializing in clinical trials in a variety of trials in therapeutic areas including vaccines, pediatrics, women's health, rheumatology, respiratory,...

Highlights:Hybrid schedule, 2 days remote per week!Lead Patient Engagement Strategy for the site!Great opportunity to make a huge impact on studiesThe CompanyOur client is a leading site network specializing in clinical trials in a variety of trials in therapeutic areas including vaccines, pediatrics, women's health, rheumatology, respiratory,...

Highlights: Hybrid schedule, 2 days remote per week! Lead Patient Engagement Strategy for the site! Great opportunity to make a huge impact on studies The Company Our client is a leading site network specializing in clinical trials in a variety of trials in therapeutic areas including vaccines, pediatrics, women's health, rheumatology, respiratory,...

Highlights:Hybrid schedule, 2 days remote per week!Lead Patient Engagement Strategy for the site!Great opportunity to make a huge impact on studiesThe CompanyOur client is a leading site network specializing in clinical trials in a variety of trials in therapeutic areas including vaccines, pediatrics, women's health, rheumatology, respiratory,...

OverviewSt. Luke's Health is the largest Catholic health system in greater Houston and southeast Texas. Our integrated delivery network comprises sixteen hospitals covering Houston, Brazos Valley, southeast Texas and Lake Jackson, and East Texas and Lufkin, and includes Baylor St. Luke's Medical Center, the research and teaching hospital for Baylor College...

Job DescriptionJob DescriptionSite Director - PsychiatryThe Site Director will ensure study enrollment to meet or exceed Sponsors' expectations, and company goals are achieved on a timely basis. The site director will also ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations...