Marcus Henderson Email & Phone Number

Duncanville, Tx, Us

Duncanville, Tx, Us

Dallas, Texas, Us

Boston, Ma, Us

• Direct Line Manager of up to 15 Study Managers• Evaluate performance on weekly basis to Increase oversight on complex studies• Increase quality of work by coaching and training employees biweekly• Collaborate with medical team(s) to create uniform standards for clinical data reporting weekly.• Uphold critical security standards when managing user access actions such as setting up and removing accounts.• Perform quality assurance reviews to verify accuracy and reliability of data.• Learn and adapt quickly to new technology and software applications.• Enforce strict data validation rules to maintain accuracy and completeness of clinical data.• Cultivate interpersonal skills by building positive relationships with clients, vendors, and medical team• Proven ability to develop and implement creative solutions to complex problems.• Implementing recruiting tools resulting in increase screening and enrollment• Drive performance of staff by creating incentives and positive work atmosphere• Administer quarterly and annual reviews to direct reports, set clear and measurable goals, action plans, and follow-up procedures

Austin, Texas, Us

• Manage over 20 Clinical Trials in 5 years with >90% study completion rate overall• Accomplish highest overall revenue gains for 2 years straight base upon study enrollment and retention• Manage study start-up process, feasibility proposal and budget collaboration• Attend and coordinate site selection visits by ensuring study site preparedness to run proposed study• Coordinate Scheduling of SIV meetings, ensuring all parties availability• Create and adhere to timeline for IRB Submissions to be completed• Provide assistance in development of data management plans and study design• Collaborate with medical teams to create uniform standards for clinical data reporting.• Minimize manual system errors with streamlined data entry process.• Act as team lead in group projects, delegating tasks and providing feedback• Demonstrate strong organizational and time management skills• Proved successful working within tight deadlines and fast-paced environment

Burlington, North Carolina, Us

• Effectively Managing and developing pipeline for Phase 1 through Phase 3 clinical studies• Making decisions independently and oversee important activities relevant to clinical research activities• Building and maintaining professional relationships with investigators and other external stakeholders• Working collaboratively with Country and Regional Operations• Building complex data analysis reports and provided timely feedback to stakeholders.• Accountable for performance and compliance with assigned protocols in relation to ICH/GCP• Applying effective time management techniques to meet tight deadlines.• Proactively driving/tracking execution and performance of deliverables• Demonstrate leadership skills in managing projects from concept to completion.

• Manage all aspects of Phase I- Phase lV Ophthalmology Clinical Trials for 5 Ophthalmologist• Propose study startup cost, negotiate study budget on behalf of site• Create study documents such as protocol and ICF for submission and approval by centralized or Local IRB• Monitor unit budget to meet financial objectives for spend rate and funding that resulted in increased revenue• Track and distribute payments to study patients for duration of trial participation• Recruit, Consent and Screen patients from within practice using EMR that lowered overall advertisement cost by 50%• Capture real time data during Cataract (Device) surgery to trigger randomization for study patient• Monitor clinical trial data entry to support timely and accurate study close-out• Proven ability to learn quickly and adapt to new systems or project changes• Developed strong organizational and communication skills through coursework and volunteer activities

Maintain accurate documentation of study patients care, condition, progress and concerns during study participation in accordance to study protocol Monitor vital signs, such as blood pressure and pulse and or any study specified procedures necessary or required per sponsor protocolComplete and verify study patients chart documentation via Electronic Data Capture in accordance with sponsor guidelines and specified database software Correspond with Sponsor team and vendors concerning regulatory documentation and responsible for the maintenance of those documents prior to the study start as well as after study close out

Collect patient data for study purpose, including vital signs, Concomitant medications, Medical History or other delegated measurements specified by sponsor. Complete and ensure the accuracy of source documents and Electronic Data Capture for source verification in accordance to sponsor guidelines in specified database provided by sponsor.Reporting to the Primary Investigator on a weekly basis on the status of any concerns involving study subjects such as Adverse Events, study recruitment and or retention

Medical Assistant, Medical/Health Management And Clinical Assistant/Specialist

Training Certification, Clinical/Medical Laboratory Science/Research And Allied Professions