Maurice Eyo Jr.

adyzxi@r.postjobfree.com 281-***-****

Personal Summary

A skilled, sagacious, and approachable Clinical Research and Project Management professional with a talent for building and maintaining relationships. Experience includes Project Management, Site Initiation Visits, Study Close-Out visits for Phase 1 Clinical Trials in Oncology involving multiple pharmaceutical sponsors. Data management experience in optometry and well versed with several sponsor and internal company study audits.

Knowledge, Skills, and Abilities:

Demonstrated understanding of medical/therapeutic area knowledge and medical terminology.

Project management with a knack for team building and recruitment.

Excellent understanding and demonstrated application of ICH GCPs, applicable regulations, and procedural documents.

Well-developed critical thinking skills, including but not limited to critical mindset, in-depth investigation for appropriate root cause analysis and problem solving.

Effective oral and written communication skills, with the ability to communicate effectively with

medical personnel

Ability to maintain customer focus through the utilization of good listening skills and attention to detail.

and the ability to perceive customers’ underlying issues.

Effective interpersonal skills

Strong attention to details

Effective organizational and time management skills

Ability to remain flexible and adaptable in a wide range of scenarios.

Ability to work in a team or independently as required.

Good computer skills: proficient knowledge of Microsoft Office and the ability to learn appropriate software.

Great English language grammar, and good presentation skills.

PROFESSIONAL EXPERIENCE

Plus+ Kam January 2020 – June 2023

Senior Project Manager

Main point of contact for all external client related communications.

Work with Account Managers to set client project expectations and build customer relationships.

Analyze, forecast, plan, schedule and implement project requirement for clients and internally for our internal project team.

Determine project scopes and lead internal project team to ensure a coordinated effort including being involved in directing, event marketing, design specifications, onsite installations etc.

Maintain detailed and accurate record keeping, including project notes, budgets, customer approvals etc.

Conduct team meetings to ensure all team members understand their roles, work requirements.

Assign tasks and deadlines for various projects to brand ambassadors and team supervisors.

Hire and train all team leads, brand ambassadors, junior project managers for client events nationally.

Manage all close out requirements for final projects including inventory counts, sales metrics etc.

Plus+ Kam May 2018 – December 2019

Brand Ambassador/Tour Manager

•Assisted in promoting and the demo of products and services on behalf of company clients.

•Maintained open communication and strong relationship with clients like (AT&T, Adidas, Conagra etc.) to ensure client event coordination success.

•Event site prospecting and negotiating event costs on behalf of clients.

•Managed company promotional vehicles driven around major cities for new product launch campaigns.

•Managed brand ambassadors across the major cities as a national tour manager organizing events across the country.

•Conducted some new product testing for clients and provided feedback for quality control.

MD Anderson Cancer Center, Houston, TX October 2015 – April 2018

(Clinical Research Coordinator II) Study Coordinator

•Managed day-to-day activities of assigned clinical oncology research protocols.

•Interviewed, screened, and recruited patients for study, explained process and procedures to educate patients regarding the research study.

•Led patient interviews to evaluate patient eligibility in the study and assisted study team and PI with study audits from the sponsors.

•Ensured proper study documents (DOAs, 1572s, CVs, financial disclosures etc.) were up to date and filed.

•Collected research data and maintained records for clinical study and regulatory documents.

•Managed research subject appointments for tests and procedures such as laboratory tests and x-rays.

•Corresponded with patient, and sponsors throughout the study.

•Ensured timely and complete reporting of AEs, SAEs, AESIs, and pregnancies, according to agreed protocol guidelines.

•Maintained rigorous communication with study monitor to ensure study sponsor was up to speed with all matter regarding studies.

•Built and maintained relationships while collaborating between cross functional study site teams.

•Worked in Investigational Cancer Therapeutic on Clinical Phase 1 trials of solid tumors.

College of Optometry at the University of Houston, Houston, TX December 2012 – September 2015

Clinical Research Data Coordinator

•Recorded data for patients undergoing cancer eye treatment and procedures via institution funded. research and assisted in the coordination of regulatory correspondence and protocol administration.

•Reviewed and summarized medical histories of patients for attending ophthalmologist.

•Assisted with coordinating all communication about quarterly audits with all necessary external auditors.

•Reported, entered, and coordinated all patient oncology data between cross functional study teams.

Research Databases:

EPIC, Medidata Classic Rave, Medidata Rave X, Datalab, InForm, ClinPlus EDC, Oracle RDC and NowEDC.

EDUCATION

BSc- Bachelor of Science in Biology The University of Houston, TX

Minor- Health The University of Houston, TX

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