Description review
Data Team Lead (Home Based - South Africa)
MMS · South Africa · back to the listing
HR standards
61/100
needs work
Title ↔ description
68/100
needs work
Reads as
Unclear
no confident match
What this role officially is
project manager — ESCO, the EU occupation classification
Project managers ensure that a project is completed on time, within budget, and that its objectives are met. They oversee the project, manage the team, ensure the most efficient resources are used and ensure that all parties involved are satisfied.
Also known as: project coordinator, project leader, special project manager, project expediter, senior project manager, project director
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What the listing never says
- 21 bullet points. Long requirement lists deter qualified candidates, who read them as hard gates. Scope clarity
- No pay range published. Candidates cannot tell whether applying is worth their time. Pay transparency
- No location or timezone policy stated, so a candidate cannot tell where they may work from. Scope clarity
The listing, marked up
Nothing in the wording of this listing tripped a check. The scores above still judge how complete and coherent it is.
Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit or follow MMS on LinkedIn.
Data Team Lead
Roles and Responsibilities
• Proficient with MS Office applications.
• Understand ICH, 21CRF Part 11, ISO 9001 and ISO 7001.
• Ability to develop eCRFs, CRF Completion Guidelines, Edit check specs, and DMP.
• Create study tracking and metric reports for use by the study team.
• Oversight of CRF tracking and data entry, integration of external electronic data, data validation and review, query processing and resolution, adverse event and medication coding, SAE reconciliation, database lock and database QC audits.
• Perform user acceptance testing (UAT) of EDC and integrated systems including development of test plan and scripts.
• Assist with preparation for training sites/users training on EDC applications, and UAT.
• End user knowledge for study conduct activities including queries management, standard reporting and extracting data in multiple EDC systems.
• Lead studies or small DM project teams for one client.
Job Requirements
• College graduate in scientific, medical, clinical discipline or related field, or related experience.
• Minimum of 5 years’ experience as a Data Team Lead or similar field required.
• Expert knowledge of scientific principles and concepts.
• Reputation as emerging leader in field with sustained performance and accomplishment.
• Proficiency with MS Office applications.
• Hands-on experience with clinical trial and pharmaceutical development preferred.
• Good communication skills and willingness to work with others to clearly understand needs and solve problems.
• Excellent problem-solving skills.
• Good organizational and communication skills.
• Familiarity with current ISO 9001 and ISO 27001 standards preferred.
• Familiarity with 21 CFR Part 11, FDA, and GCP requirements.
• Basic understanding of CROs and scientific & clinical data/terminology, & the drug development process.
Should you not receive a response on your application within 14 days, please consider your application unsuccessful.
Originally posted on Himalayas
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit or follow MMS on LinkedIn.
Data Team Lead
Roles and Responsibilities
• Proficient with MS Office applications.
• Understand ICH, 21CRF Part 11, ISO 9001 and ISO 7001.
• Ability to develop eCRFs, CRF Completion Guidelines, Edit check specs, and DMP.
• Create study tracking and metric reports for use by the study team.
• Oversight of CRF tracking and data entry, integration of external electronic data, data validation and review, query processing and resolution, adverse event and medication coding, SAE reconciliation, database lock and database QC audits.
• Perform user acceptance testing (UAT) of EDC and integrated systems including development of test plan and scripts.
• Assist with preparation for training sites/users training on EDC applications, and UAT.
• End user knowledge for study conduct activities including queries management, standard reporting and extracting data in multiple EDC systems.
• Lead studies or small DM project teams for one client.
Job Requirements
• College graduate in scientific, medical, clinical discipline or related field, or related experience.
• Minimum of 5 years’ experience as a Data Team Lead or similar field required.
• Expert knowledge of scientific principles and concepts.
• Reputation as emerging leader in field with sustained performance and accomplishment.
• Proficiency with MS Office applications.
• Hands-on experience with clinical trial and pharmaceutical development preferred.
• Good communication skills and willingness to work with others to clearly understand needs and solve problems.
• Excellent problem-solving skills.
• Good organizational and communication skills.
• Familiarity with current ISO 9001 and ISO 27001 standards preferred.
• Familiarity with 21 CFR Part 11, FDA, and GCP requirements.
• Basic understanding of CROs and scientific & clinical data/terminology, & the drug development process.
Should you not receive a response on your application within 14 days, please consider your application unsuccessful.
Originally posted on Himalayas