Data Entry Clinical

CURRICULUM VITAE

Mohau La-Donna Kapa

PROFILE

CONTACT

HOBBIES

ACQUIRED SKILLS

EXPERIENCE

I am self- motivated and determined person who prefers to secure a position in an environment that offers improvement for growth. I work well under pressure. I am also a proactive team player and able to multitask. I possess very strong attributes that would be useful in the working environment. I am a fast learner and always keen to acquire new

knowledge. I hope my skills and academic background will make me a strong candidate for the vacancy

**-*****.****@*******.**.**

+27 (0-84-842-****

Crimson Square,

Fairview Avenue

Woodstock

Photography

Music Writing

Reading

Central University of Technology

National Diploma Clinical Technology Pulmonology

2008

Brebner High School

National Senior Certificate

2003

Task Applied Science

Project management/ Study Coordinator

Jun 2018 - Present

Duties:

Maintaining and co-ordinating the logistical aspects of clinical trials according to GCP the study protocol and the standard operating procedures

Undertaking recruitment, screening, enrolment, and follow-up of eligible subjects including sourcing subjects from primary healthcare clinic visits and telephonically pre-screening subjects responding to advertising

activities.

MS Office

Excellent sales and negotiation skills

Communication (verbal and written).

Strong administrative skills.

Strong interpersonal skills.

Good planning, management, organization and co-

ordination skills.

EDUCATION

Maintaining accurate and complete documentation, including but not limited to regulatory documents, signed informed consent forms, ethics committee approvals, source documentation, drug dispensing logs, subject and screening logs and study-related communications. Subject and screening logs and study-related communications. ·

Quality control of clinical source notes resolving queries and missing data. Data entry from clinical source notes onto paper or electronic case report forms.

Desmond Tutu HIV Centre (Emavundleni)

Study Coordinator

Jun 2016- May 2018

Duties:

Maintaining and co-ordinating the logistical aspects of clinical trials according to GCP the study protocol and the standard operating procedures

Undertaking recruitment, screening, enrolment, and follow-up of eligible subjects including sourcing subjects from primary healthcare clinic visits and telephonically pre-screening subjects responding to advertising activities.

Maintaining accurate and complete documentation, including but not limited to regulatory documents, signed informed consent forms, ethics committee approvals, source documentation, drug dispensing logs, subject and screening logs and study-related communications. Subject and screening logs and study-related communications. ·

Quality control of clinical source notes resolving queries and missing data. Data entry from clinical source notes onto paper or electronic case report forms.

University of Cape Town Lung Institute

Clinical Technologist/ Study Coordinator

Jan 2010-May 2016

Duties:

Maintaining and co-ordinating the logistical aspects of clinical trials according to GCP the study protocol and the standard operating procedures

Undertaking recruitment, screening, enrolment, and follow-up of eligible subjects including sourcing subjects from primary healthcare clinic visits and telephonically pre-screening subjects responding to advertising activities.

Communication of all protocol-related issues to the appropriate management staff or study sponsor, including questions regarding the conduct of the study, concerns regarding possible adverse events or subject compliance.

Study subject clinical contact activities, including taking history, performing phlebotomy, pulmonary function tests and echocardiogram

PAREXEL

Clinical Technologist/ Study Coordinator

Aug 2008- Dec 2009

Duties:

Maintaining and co-ordinating the logistical aspects of clinical trials according to GCP the study protocol and the standard operating procedures

Undertaking recruitment, screening, enrolment, and follow-up of eligible subjects including sourcing subjects from primary healthcare clinic visits and telephonically pre-screening subjects responding to advertising activities.

Management of all operational aspects of the study, including timeliness in completing case report forms, data entry, reporting adverse events, managing caseload and managing study files.

Communication of all protocol-related issues to the appropriate management staff or study sponsor, including questions regarding the conduct of the study, concerns regarding possible adverse events or subject compliance. REFERENCES

Miss Goodness Mvuyane 071-*******

Site Coordinator Desmond Tutu HIV Centre (Emavundleni) Mrs Helana Olkers 021-***-****

Senior clinical technologist UCT Lung institute

Mrs Marina Pretorius 082-***-****

Chief Clinical Technologist Universitas Acedamic Hospital Universitas Hospital

Student Clinical Technologist

Jan 2007- Jul 2008

Duties:

Performing and calculating the following pulmonary function studies: spirometry, lung volume measures using whole body plethysmography, diffusion capacity and maximal respiratory pressures.

Explaining specified methods of breathing and procedures to patients or family member(s) when applicable.

Maintaining confidentiality of all patient information according to federal and state guidelines and regulations.

Performing other duties as assigned.

Contact this candidate