Andre Weeks Email & Phone Number

Philadelphia, Pennsylvania, United States

Chicago, Illinois, US

• Demonstrates ability with integrated CRM software system and success in data entry;
• Uses highly detail-oriented skills with project management skills to take the initiative and check work for accuracy and;
• Takes initiative to research and investigate missing data.

• Develops trial protocols and questionnaires for submission to the Institutional Review Board for laser treatment on multiple maladies such as Alzheimer’s and dementia;
• Reviews numerous funding opportunities for the company’s research projects;
• Prepares deadline-based applications for funding and;
• Builds effective relationships with other research professionals via networking and phone calls.

• Films, edits, and posts video content for clients such as Buffalo Cherry Blossom Festival and Western New York Alzheimer’s Association;
• Photographs graduations, poetry readings, concerts, and fundraisers;
• Designs advertising for ongoing promotion for participation in research with Buffalo Healthy Living magazine and;
• Receives awards for work such as Best Drone Photo and Editor’s Choice.

US

I have about 2 years as a CTM, approximately 4 years of industry experience, and 11 years total in the clinical research field.

US

I have about 5 years as a CRA, approximately 4 years of industry experience, and 11 years total in the clinical research field.

US

I have about 2 years as a CTM, approximately 4 years of industry experience, and 11 years total in the clinical research field

Ahmedabad, Gujarat, IN

• Identifies and qualifies potential investigators to ensure that sites have adequate time and can fulfil their obligation to the study;
• Responsible for identification and collection of all necessary documents to be forwarded to the Project Manager/designee in order to check site feasibility and approval from authorities;
• Prepares other colleagues for regulatory and EC submissions and in the generation of Financial Agreements;
• Generates study budgets and ensures timely payments are made to the site;
• Conducts monitoring visits to check compliance with study management, protocol, and other requirements;
• Trains study team regarding the monitoring plan, recording and maintenance of essential documents for start-up activities and site initiation;

Wayne, Pennsylvania, US

• Responsible for all operational aspects and progress of clinical trial from a study planning activity to study execution including ongoing tracking of all applicable performance metrics and quality indicators at.
• Served as an escalation point and resource for study team and investigational sites;
• Oversaw site feasibility/selection processes;
• Developed subject recruitment/retention strategy and related initiatives;
• Provided operational and strategic input and/or approves study documents such as synopsis, protocol, ICF, CRFs, CRF Completion Guidelines, Study Plans, Clinical Study Report (CSR) development, etc.;
• Participated in the review of clinical data; provides guidance on issues/queries as needed and implements risk management concepts as appropriate;

Lower Gwynedd, PA, US

• Coordinated with contract research organizations (CROs) in the preparation and submission of documents necessary for clinical studies;
• Prepared case report forms;
• Managed two clinical trial associates;
• Monitored and managed data;
• Communicated with key opinion leaders (KOLs), primary investigators (PIs), or other relevant stakeholders and;
• Ensured smooth execution of company sponsored clinical studies.

• Implemented and oversaw the daily operations of conducting clinical research trials at the University of Pennsylvania Women's Health Clinical Research Center;
• Assisted in the coordination of all research projects;
• Integrated research activities into the clinical flow;
• Responsible for personnel management of the research team and;
• Supported the director of clinical research operations in all aspects of clinical trial development within the division.

Philadelphia, PA, US

• Managed and conducted qualification, initiation, monitoring, and closeout visits for research site in compliance with 7 approved protocols;
• Communicated with the medical site staff including coordinators and multiple clinical research physicians and their staff;
• Verified adequate investigator qualifications, training, and resources, including facilities, laboratories, equipment, and staff;
• Confirmed medical records and research source documentation against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to, and.
• Authenticated the investigator is enrolling only eligible subjects;
• Reviewed regulatory documents;

Amherst, New York, US

• Managed the OlympiA phase III breast cancer clinical trial database;
• Reviewed and validated clinical trial data (patient history, treatment, Adverse Events, follow-up, etc.);
• Tasked with discrepancy checking and querying;
• Developed and reviewed data management documentation (protocols, manuals, case report forms, etc.);
• Produced of quality control reports and;
• Supported site personnel via email, phone or trainings.

Columbia, MD, US

• Performed an analysis on Alzheimer's diagnosis procedures on multiple cohort studies in the United States including Mayo Clinic, NYU and many others.
• Researched and completed a report on the “Global Public Health Threat of Blindness” for Bayer
• Investigated different countries' policies on blindness prevention.
• Explored the trends of aging and eye health in US and non-US markets

Amherst, New York, US

• Implemented a phase III double blinded placebo-controlled clinical trial regarding Lamotrigine and Ménière's Disease;
• Developed drug trials and communicated with pharmacists to organize the trials;
• Determined if subjects were eligible and then regulated their participation
• Statistically analyzed data using means, medians, modes, standard deviations, multiple regression, and multivariate analysis.
• Managed and updated the research database of over 2,800 subjects accurately and designed various sub-databases
• Mined and collected data from medical records.

• Organized and helped analyze current data sources that are county specific
• Compared local data with regional, NYS, and Healthy People 2020 indicators
• Worked with P2 intern to analyze results of County CHA Survey, administered both in hard copy and by Survey Monkey
• Participated in summer meetings and conference calls as scheduled with CHA/CSP team to begin writing CHIP

• Looked at data with Neurology PhD candidate
• Tested Mediation Factors
• Mined a Neuropsychology Database
• Performed multivariate, correlative analyses.

Master'S Degree, Public Health: Biostatistics

Bachelor Of Science, Biological Sciences And Mathematics