Register
Recruit Create CV

Clinical Trial Management Jobs in Union, Arkansas

Remote - Senior Clinical Trial Specialist
By Beacon Hill Staffing Group At United States
5+ years previous clinical research experience in clinical trial coordination, site management, and or vendor management.
Must have the ability to build and maintain positive relationships with management and peers
Manage the collection, review and approval of regulatory documents from clinical sites
Manages and tracks study specific payments
Manage ancillary vendors, such as a specialty lab
Review site visit reports, under the direction of the Clinical Program Manager or designee
Clinical Trial Monitor Jobs
By Medasource At United States
Monitor clinical trial progress through a combination of remote data review and on site monitoring visits. Some travel will be required.
3+ years of progressively responsible clinical trials experience with 2+ years of monitoring experience.
Assist in the development and writing of clinical trial monitoring plans.
Provide recommendations and guidance to study specific monitoring teams and assist in audit readiness and preparation.
Participate in regular monitoring team group meetings.
Bachelor's degree in a field relevant to research compliance
Clinical Trial Assistant Jobs
By Advanced Recruiting Partners At United States

Support for Study Start-up and Close-out: Contribute to study start-up and close-out activities, including site initiation, investigator meetings, and archiving processes.

Clinical Trial Manager - 98102
By Medix™ At United States
Manages CRO, including overseeing clinical monitoring, investigational selection and site management
Manages, provides guidance and oversight for all components of a clinical trial from protocol development through clinical study report
Helps develop and manage clinical budgets and contracts plans for clinical trials.
Develops and contributes to development of study plans and manuals
Collaborates with CRO and investigational sites, as needed, to complete and execute trial deliverables as required per protocol and contract.
Responsible for oversight of Trial Master File (TMF) for inspection readiness.
Vice President Clinical Trial Management
By Apsida Life Science At United States
Experience in successfully leading global CRO Project Management or Clinical Trial Management teams.
Previous experience and proven ability to lead staff, think strategically, and execute organizational strategy.
Masters or PhD in life sciences/medical field;
Clinical Trial Monitoring Specialist
By Infosoft, Inc. At United States
3-5 years of experience required
Experience with medical device monitoring is required.
Experience with cardiac trials and/or blinded trials is preferred.
Experience with Medidata RAVE and Medidata CTMS is preferred.
Remote with frequent travel to clinical sites (Pacific or Mountain Time Zone)
remote and onsite monitoring activities
Clinical Trial Supply Chain Specialist
By Mindlance At United States
SAP software based computer systems experience.
MS Office and MS Teams experience.
SKYPE Meeting or Virtual Meeting software experience.
GMP and Pharmaceutical Industry Regulations knowledge.
Ability to learn multiple computer systems.
Clinical Trial Liaison Jobs
By Mirum Pharmaceuticals, Inc. At United States
Clinical site management experience, with an understanding of the operational aspects of clinical research and clinical development outsourcing
Excellent written and verbal communication skills - able to interact with all levels of internal and external management
Self-motivated with proactive issue monitoring and management including risk assessment and contingency planning
Other tactical or strategic requirements in line with the study team
5 years’ experience in clinical research in Pharma, Biotech or CRO or related experience
Demonstrated experience of working directly with clinical sites and investigators
Sr Consultant, Clinical Trial Compliance, Audit, & Inspection Readiness
By EG Life Sciences At United States
5+ years of Global Pharmaceutical Clinical Study Management:
1) 10+ years of Clinical Research Experience:
Audit & Inspection Readiness Experience:
ADDITIONAL QUALIFICATIONS / NICE TO HAVES
1) GCP and Clinical Quality experience
Sr Consultant, Clinical Trial Compliance, Audit, & Inspection Readiness
Clinical Trial Associate Jobs
By NuWest Group At United States
• Excellent communication, time management and organizational skills
• Work with the clinical operations team to prepare metrics and updates for management
• 2+ years of experience in a clinical operations role in the biopharmaceutical industry
• Experience planning and tracking deliverables and timelines
• Take ownership of assigned responsibilities, with guidance
• Specific experience in Lymphoma or CAR T trials
Clinical Trial Contract Manager
By Mindlance At United States
·Experience of Study Management within a pharmaceutical or clinical background
·Knowledge of relevant legislation and new developments in the area of Clinical Development and Study Management
o Manager would like to see candidates with Clinical Research experience.
·Understanding of multiple aspects within Study Management
Pricing and Contract Strategy Manager
o Looking for someone that has experience that has negotiating contact language and budgets with clinical contracts.
Clinical Trial Project Manager
By SRG At United States
3 years of relevant clinical research and project management experience with a CRO, pharmaceutical, biotechnology / device company
Strong project management skills including client management, fiscal / contract management, and quality management
Perform contract and financial management activities for assigned trials and serve as central point of contact with sponsor for project updates
Oversee all aspects of clinical research projects to assure applicable regulations, standard operating procedures, and sponsor requirements are met.
Bachelor’s Degree or equivalent experience
Good knowledge of FDA guidelines and review processes, IND and NDA processes, and GCPs
Clinical Trial Coordinator - Monitoring (Remote)
By Merck At United States
Effective time management, organizational and interpersonal skills, conflict management
Clinical supply & non-clinical supply management, in collaboration with other country roles
Manage Labeling requirements and coordinate/sign translation change request, in collaboration with other country roles (if applicable)
Ensure proper provisioning for Learning Management System (CLMS) for all study site staff.
Credit Management within Learning Management System
Excellent negotiation skills for CTCs in finance area
Clinical Trial Manager Jobs
By Advanced Recruiting Partners At United States
· Maintains compliance in assigned region or project for performance, deliverables, and associated KPI’s.
· Ensures alignment of clinical activities to budget, including identification of out of scope activities.
· May participate in business development proposals, defense meetings and proposal development.
Clinical Trial Disclosure Manager
By MSI Pharma At United States
Bachelor’s degree in a scientific/medical/pharmaceutical discipline (other commensurate qualifications and/or related experience in industry considered if equivalent)
Working experience with global clinical transparency regulations, eg EMA Policy 0070, Health Canada PRCI, EU Clinical Trial Regulation 536/2014
At least 3 years working in a Clinical Development and/or regulatory affairs environment
Sound understanding of the drug development process
Awareness of the Clinical Trial Application process and/or the contents of the clinical modules of the Marketing Authorization Application
Awareness of privacy regulations, eg GDPR
Clinical Trial Specialist Jobs
By Hawthorne Effect, Inc. At United States
Strong organization skills with experience with balancing priorities and resources.
Visit Management: Support logistics and visit scheduling teams by communicating relevant study information to Clinical Success team
Clinical Trial Experience is highly preferred but not required.
Strong skills in the use of technology, tools, operating systems, and software and is comfortable using these daily.
A creative and resourceful problem-solver with strong critical thinking skills.
GCP and good documentation practice expertise is required
Clinical Trial Assistant / Trial Documentation (Tmf)
By Apex Systems At United States
1. Provide start-up and ongoing trial regulatory document management
5. Setup and manage regulatory document trackers/reports as assigned.
6. Maintain a professional approach respecting the dignity and confidentiality of associates, manager, and vendors.
11. Maintain CEUs for SOCRA or ACRP certification.
• Oncology experience preferred. Prior experience managing flow of clinical trial regulatory documents preferred
4. Ensure quality product deliverables at all times.
Clinical Trial Manager Jobs
By Astrix At United States
Strong project management and team leadership capability
Leads local trial team to ensure integrity of trial conduct, assurance of patient safety, in line with regulatory requirements
Leads the local trial team as an OPU Clinical Trial Manager (CTM) Trial Preparation, Conduct and Closeout
B.S., M.S., or PhD plus a minimum of 3 years of experience in clinical research in pharmaceutical industry
Knowledgeable across all aspects of clinical trial operations and execution.
In collaboration with Site Monitoring Lead and CRAs, ensure Trial contact for CRAs, investigators and site staff.
Clinical Trial Document Management (Ctdm) Specialist
By Alcon At United States
Enter and maintain site information and document tracking in current clinical trial management systems.
Travel Requirements: minimal to no travel if located in Fort Worth; less than 10% if remote
Bachelor’s Degree or Equivalent years of directly related experience (or high school +8 yrs; Assoc.+4 yrs)
Basic knowledge of clinical trial processes
Alcon provides a robust benefits package including health, life, retirement, flexible time off, and much more!
Benefit from working in a highly collaborative and diverse environment, as well as within a welcoming and empowered team.
Senior Clinical Trial Manager
By Tourmaline Bio At United States
Strong working knowledge of cGCP/ ICH guidelines, and US and international clinical regulatory requirements
Develop and manage clinical trial budget and facilitate contract review
Adhere to relevant company policies and SOPs, cGCP/ICH guidelines, QC/QA procedures, as well as relevant clinical regulatory requirements
Advanced degree or certification is a plus
5+ years of clinical trial operations experience in a biotech, pharmaceutical, CRO, clinical research site or related healthcare company
Experience working on a multi-phase clinical program is a plus

Do you want to make a difference in the lives of patients? Join our team as a Clinical Trial Manager and help us bring innovative treatments to the world!

Overview of Clinical Trial Management Clinical Trial Management is a specialized field of healthcare that involves the management of clinical trials. Clinical Trial Managers are responsible for the planning, coordination, and execution of clinical trials. They work with research teams, sponsors, and regulatory agencies to ensure that clinical trials are conducted in accordance with applicable regulations and standards. Clinical Trial Managers are also responsible for the development of protocols, the recruitment of participants, and the collection and analysis of data. Detailed Job Description of Clinical Trial Management Clinical Trial Managers are responsible for the planning, coordination, and execution of clinical trials. They work with research teams, sponsors, and regulatory agencies to ensure that clinical trials are conducted in accordance with applicable regulations and standards. Clinical Trial Managers are responsible for developing protocols, recruiting participants, and collecting and analyzing data. They must also ensure that all safety and ethical standards are met. Clinical Trial Managers must be able to effectively communicate with research teams, sponsors, and regulatory agencies. They must also be able to manage budgets and timelines. Clinical Trial Management Job Skills Required
• Knowledge of clinical trial regulations and standards
• Excellent communication and organizational skills
• Ability to manage budgets and timelines
• Ability to work independently and as part of a team
• Knowledge of data collection and analysis methods
• Knowledge of safety and ethical standards
Clinical Trial Management Job Qualifications
• Bachelor’s degree in a related field
• Experience in clinical research or clinical trial management
• Certification in clinical trial management (preferred)
• Knowledge of applicable regulations and standards
Clinical Trial Management Job Knowledge
• Knowledge of clinical trial regulations and standards
• Knowledge of data collection and analysis methods
• Knowledge of safety and ethical standards
• Knowledge of applicable regulations and standards
Clinical Trial Management Job Experience
• Experience in clinical research or clinical trial management
• Experience in budget and timeline management
• Experience in working with research teams, sponsors, and regulatory agencies
Clinical Trial Management Job Responsibilities
• Develop protocols for clinical trials
• Recruit participants for clinical trials
• Collect and analyze data from clinical trials
• Ensure that safety and ethical standards are met
• Manage budgets and timelines for clinical trials
• Communicate with research teams, sponsors, and regulatory agencies