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Malvyn Fairclough
Nationality: British
Date of birth: 17/09/1993
https://malvynfairclough.wordpress.com
Contact me
 + 44 7 528 802 302
 malvynfairclough@outlook.com
 124 Kerridge court,
Balls pond road,
N14AN, London
uk.linkedin.com/in/MalvynFairclough
Abstract
Motivated UK-based
professional, possessing a strong
background in pharmaceutical
sciences and management.
Most recent work experience as
a Project Associate for PRA
Health Sciences. Interested in
securing a position within Data
Science and willing to relocate.
My adaptive capabilities ensure
constant improvements in
productivity without sacrificing
of end product quality.
MSc modules
Process of Drug Discovery 71%
Pharma Management 69%
Modern Aspect of Drug Dvpt. 71%
Academic Dissertation 70%
BSc modules
Clinical Diagnosis 62%
Cell Biology (Oncology) 79%
Pharmacology & Toxicology 73%
Neuroscience 71%
Molecular Biology 79%
Education:
Work Experience:
Drug Discovery & Pharmaceutical Management MSc 2014-15,
University College London (UCL)
Skills gained:
 Source document and eCRF data verification training.
 Database training (PubMed, ClinicalTrials.gov, EU Clinical Trials
Register)
 Assimilation of ICH-GCP guidelines
 Familiarity with clinical trial EDC software e.g. InForm 5.5
 Performing Business valuations for mergers and acquisitions
 Performing statistical analysis and establishing results
significance
Degree Classification: Distinction
Biomedical Science BSc 2011–14,
Royal Holloway University of London (RHUL)
Skills gained:
 Effective analysis and interpretation patient anamnesis
 Familiarity with project management in a preclinical lab setting
 Rapid detection of anomalous results via well-tested analytical
skills, developed through recording and processing of data
 Great understanding of the human anatomy as well as the
cellular & molecular mechanisms underlying various medical
conditions spanning across several scientific areas
Degree Classification: First Class
Project Associate – PRA Health Sciences
February 2016 – May 2016
Role within internationally acclaimed CRO providing administrative
support and other project management deliverables. As an
integral member of the PRA team, I actively participated in
project startup and execution in collaboration with multiple top
Pharma clients of varying therapeutic expertise e.g. oncology.
Responsibilities:
 Communicating with Principal Investigators and lead CRAs to get
updates on patient health and collected samples status
respectively
 Facilitating project team and client meetings/teleconferences,
through scheduling, booking resources and preparing meeting
materials, agendas and meeting minutes
 Developing and maintaining project tracking tools and generating
project status reports from weekly raw data
 Remote tracking and archival of pending essential documents
e.g. Suitability of facilities forms, Protocol amendments and ICFs
 Facilitating team compliance through recurrent quality control
and follow up, e.g. project specific training, CTMS and TMF
QC/compliance
Research Laboratory Scientist
Sept 2013 – May 2014
Lab-based research project with aim of understanding the resistance of bacteria to antibiotics. In
this project, I was tasked with investigating the sociality of susceptible & resistant bacterial
populations in order to shed light on potential non-genetic factors involved in developed
antimicrobial resistance.
Responsibilities:
 Design and develop laboratory protocols and independently conduct practical experiments
 Performing MIC Assays, Broth/Agar Bacterial Competition Assays and Cell Cytometry
 Engaging with mathematical and statistical data handling
 Drafting and dispatching of monthly progress reports to the supervising senior researcher
Private Biology Tutor
Jul – Aug 2012 and Jul - Aug 2013
Private remedial teaching lessons of Baccalaureate level Biology to students having difficulties
with the subject at hand. Through this experience I further developed my communication,
thought structuring and receptive skills due to having to teach in such a way as to share a
maximum amount of information in easy to absorb, yet concise explanations in order to provide
an accurate depiction of the topics at hand.
Responsibilities:
 Organising study plans for tutees
 Ensuring that said study plans are assimilated and respected by tutees
 Succeeding in completing the self-appointed objective of aiding tutees to raise their
academic average by 20%
Intern at Sans-Souci clinic
Feb 2011
Month-long internship through which I experienced professional life within a clinical setting, gaining
skills such as the abilities to comfortably interact with patients, to quickly adapt to new
environments and to maintain professional integrity.
Responsibilities:
 Supervised dispensing of prescribed medication to clinic patients
 Shadowing of healthcare professional throughout his counseling sessions with patients
 Participating in group activities and attending staff meetings
Languages
Mastery Fluent (mother tongue) Fluent (mother tongue) Conversational
IT
MS Office
Mastery Intermediate Intermediate Intermediate Advanced
Interests: Block-chain technology, algorithmic trading, 3D printing, musical composition (piano
and guitar), coding, cinematography, competitive sports and travelling.

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Malvyn Fairclough Data Science CV

  • 1. Malvyn Fairclough Nationality: British Date of birth: 17/09/1993 https://malvynfairclough.wordpress.com Contact me  + 44 7 528 802 302  malvynfairclough@outlook.com  124 Kerridge court, Balls pond road, N14AN, London uk.linkedin.com/in/MalvynFairclough Abstract Motivated UK-based professional, possessing a strong background in pharmaceutical sciences and management. Most recent work experience as a Project Associate for PRA Health Sciences. Interested in securing a position within Data Science and willing to relocate. My adaptive capabilities ensure constant improvements in productivity without sacrificing of end product quality. MSc modules Process of Drug Discovery 71% Pharma Management 69% Modern Aspect of Drug Dvpt. 71% Academic Dissertation 70% BSc modules Clinical Diagnosis 62% Cell Biology (Oncology) 79% Pharmacology & Toxicology 73% Neuroscience 71% Molecular Biology 79% Education: Work Experience: Drug Discovery & Pharmaceutical Management MSc 2014-15, University College London (UCL) Skills gained:  Source document and eCRF data verification training.  Database training (PubMed, ClinicalTrials.gov, EU Clinical Trials Register)  Assimilation of ICH-GCP guidelines  Familiarity with clinical trial EDC software e.g. InForm 5.5  Performing Business valuations for mergers and acquisitions  Performing statistical analysis and establishing results significance Degree Classification: Distinction Biomedical Science BSc 2011–14, Royal Holloway University of London (RHUL) Skills gained:  Effective analysis and interpretation patient anamnesis  Familiarity with project management in a preclinical lab setting  Rapid detection of anomalous results via well-tested analytical skills, developed through recording and processing of data  Great understanding of the human anatomy as well as the cellular & molecular mechanisms underlying various medical conditions spanning across several scientific areas Degree Classification: First Class Project Associate – PRA Health Sciences February 2016 – May 2016 Role within internationally acclaimed CRO providing administrative support and other project management deliverables. As an integral member of the PRA team, I actively participated in project startup and execution in collaboration with multiple top Pharma clients of varying therapeutic expertise e.g. oncology. Responsibilities:  Communicating with Principal Investigators and lead CRAs to get updates on patient health and collected samples status respectively  Facilitating project team and client meetings/teleconferences, through scheduling, booking resources and preparing meeting materials, agendas and meeting minutes  Developing and maintaining project tracking tools and generating project status reports from weekly raw data  Remote tracking and archival of pending essential documents e.g. Suitability of facilities forms, Protocol amendments and ICFs  Facilitating team compliance through recurrent quality control and follow up, e.g. project specific training, CTMS and TMF QC/compliance
  • 2. Research Laboratory Scientist Sept 2013 – May 2014 Lab-based research project with aim of understanding the resistance of bacteria to antibiotics. In this project, I was tasked with investigating the sociality of susceptible & resistant bacterial populations in order to shed light on potential non-genetic factors involved in developed antimicrobial resistance. Responsibilities:  Design and develop laboratory protocols and independently conduct practical experiments  Performing MIC Assays, Broth/Agar Bacterial Competition Assays and Cell Cytometry  Engaging with mathematical and statistical data handling  Drafting and dispatching of monthly progress reports to the supervising senior researcher Private Biology Tutor Jul – Aug 2012 and Jul - Aug 2013 Private remedial teaching lessons of Baccalaureate level Biology to students having difficulties with the subject at hand. Through this experience I further developed my communication, thought structuring and receptive skills due to having to teach in such a way as to share a maximum amount of information in easy to absorb, yet concise explanations in order to provide an accurate depiction of the topics at hand. Responsibilities:  Organising study plans for tutees  Ensuring that said study plans are assimilated and respected by tutees  Succeeding in completing the self-appointed objective of aiding tutees to raise their academic average by 20% Intern at Sans-Souci clinic Feb 2011 Month-long internship through which I experienced professional life within a clinical setting, gaining skills such as the abilities to comfortably interact with patients, to quickly adapt to new environments and to maintain professional integrity. Responsibilities:  Supervised dispensing of prescribed medication to clinic patients  Shadowing of healthcare professional throughout his counseling sessions with patients  Participating in group activities and attending staff meetings Languages Mastery Fluent (mother tongue) Fluent (mother tongue) Conversational IT MS Office Mastery Intermediate Intermediate Intermediate Advanced Interests: Block-chain technology, algorithmic trading, 3D printing, musical composition (piano and guitar), coding, cinematography, competitive sports and travelling.