Parexel Vacancies 2022 in South Africa

Parexel Job Vacancies 2022 notification out for Clinical Data Analyst Jobs. Apply for Parexel Jobs in South Africa. Check Latest Parexel Government Jobs in Gauteng. How to Apply for Parexel Vacancies at Official Parexel Careers Portal. Find out here Upcoming Centurionn Jobs Careers24 News at www.parexel.com.


Parexel Vacancies 2022 Apply for Clinical Data Analyst Jobs in Centurion

Parexel has released a Clinical Data Analyst job notification at www.parexel.com Careers website. Parexel has displayed vacant seats for the post of Clinical Data Analyst vacancies. Candidates satisfying the desired eligibility conditions as mentioned in the Parexel official notification can submit their application in the prescribed format on before last date with the help of details given below-
NOTE:- Candidates are suggested to read the original Parexel job notification before applying for desired post.

Name of Available Job Post ⇒ Clinical Data Analyst
Name of Vacancies ⇒ Parexel Vacancies 2022
Job Location ⇒ Jobs in Centurion
Salary ⇒ R 266,000.00 Yearly
Last Date ⇒ Untill Fill

Parexel Job Description

Role responsibilities:

  • Provide data management input on Clinical Trial teams. May have the role of TDM on small low complexity trials
  • Performs DM activities for start up of a study including preparing the eCRF, CCGs where needed, Data Handling plan (DHP) Data Review Plan (DRP) and performing user acceptance testing (UAT) as applicable
  • Manage local lab set up for the Clinical Database as applicable
  • Under supervision ensures consistency of assigned trials with program level standards
  • Understands third party data requirements and begins to gather an understanding of new technologies that may be used in the course of clinical trials
  • Performs ongoing review of all data generated from the clinical study including Third party and local lab data as well as SAE reconciliation where applicable
  • Ensures activities that are performed are done with quality and understanding of the process
  • Verifies and tracks eCRF completion including Query resolution and provides data status updates as needed
  • With support from the Trial Data Manager develops proposals to resolve issues that may occur during the running of assigned trials
  • With support from the Trial Data Manager gives input into Study Specification worksheets should assigned trials need to be outsourced
  • Has a working knowledge of FDA and ICH guidelines
  • Has proven ability to use the tools available to generate listings for data review and where necessary provides these to the study teams. Generates the study status reports for use at Clinical trial team meetings

Qualifications

Role requirements:

  • University or college degree in life science, pharmacy, nursing or equivalent relevant degree
  • Fluent English (oral and written)
  • Ideally 3 years experience in Drug Development with at least 2 years in Clinical Data Management

Apply Now

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Parexel Vacancies 2022 Apply for Project Specialist Jobs in South Africa

Parexel has released a Project Specialist job notification at www.parexel.com Careers website. Parexel has displayed vacant seats for the post of Project Specialist vacancies. Candidates satisfying the desired eligibility conditions as mentioned in the Parexel official notification can submit their application in the prescribed format on before last date with the help of details given below-
NOTE:- Candidates are suggested to read the original Parexel job notification before applying for desired post.

Name of Available Job Post ⇒ Project Specialist
Name of Vacancies ⇒ Parexel Vacancies 2022
Job Location ⇒ Jobs in South Africa
Salary ⇒ R 312,000.00 Yearly
Last Date ⇒ Untill Fill

Parexel Job Description

Key Accountabilities:

• Updating and customizing of systems and tools according to applicable SOP’s
• Study reporting and analysis with subsequent highlighting issues for project team. Maintenance of systems and tools according to applicable SOP’s.
• Responsible for drafting a consistent coherent project management plan, including coordinated planning of the different project activities and input from the different functions. The plan covers all parts of the project to be integrated together (scope, CIS, risk plan, quality plan, communication plan, schedule, procurement plan, and resource plan). Responsible for updating the project plan as needed and collaborating with the PL to execute the plan and close the project.
• Project meetings preparation and attendance; support preparation of required information for project review meeting; reporting of owned responsibilities during meeting attendance; support tracking and follow-up of action items.
• Collaborate with PL and PMs to ensure study supplies are delivered as required and according to contract obligation. Assist PM with vendor selection.
• Collaborate with the PL and PMs in the resourcing process. Processing pass through cost invoicing, third-party invoicing, generating Purchase Orders, monthly review of project labor hours, maintenance of project TIME Codes.
• Collaborates with PL/PM on ensuring that systems are closed, documents archived and final work handed-over to the sponsor.

Qualifications

Skills:

• Excellent interpersonal, verbal and written communication skills, as the exchange of information is a significant part of the job
• Attention to detail and quality of work
• Client focused approach to work
• A flexible attitude with respect to work assignments and new learning
• Ability to manage multiple and varied tasks with enthusiasm and prioritize workload
• Willingness to work in a matrix environment and to value the importance of teamwork
• Problem solving and judgement ability

Knowledge and Experience:

• Relevant experience in the PS/ or similar role desired
• Basic knowledge of activities and procedures of the work area

Education:

• Intermediate to Advanced English level for non-native English speakers
• Bachelor’s degree or equivalent degree
• Master’s degree, post-graduation or equivalent desired

Apply Now

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Parexel Vacancies 2022 Apply for Senior Clinical Research Associate Jobs in South Africa

Parexel has released a Senior Clinical Research Associate job notification at www.parexel.com Careers website. Parexel has displayed vacant seats for the post of Senior Clinical Research Associate vacancies. Candidates satisfying the desired eligibility conditions as mentioned in the Parexel official notification can submit their application in the prescribed format on before last date with the help of details given below-
NOTE:- Candidates are suggested to read the original Parexel job notification before applying for desired post.

Name of Available Job Post ⇒ Senior Clinical Research Associate
Name of Vacancies ⇒ Parexel Vacancies 2022
Job Location ⇒ Jobs in South Africa
Salary ⇒ R 840,000.00 Yearly
Last Date ⇒ Untill Fill

Parexel Job Description

Parexel FSP is currently seeking Senior Clinical Research Associates & CRAII, home-based, Johannesburg.

Working as a Clinical Research Associate at Parexel FSP offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors including the leading global biotechs and Pharma top 50. And we have an incredible pipeline of work.

Whether you see your future path as a CRA, or in fields such as clinical operations, project management, line management, or other positions, we have a world of opportunity waiting for you.
Our CRAs work from their home office base, supporting studies within their country or region. ‘Manageable sites, manageable protocols’ is our mantra. Expect exciting professional challenges in inspiring studies, but with time for your outside life.

Some specifics about this advertised role

Dedicated to one client.

Responsible for all site management and monitoring activities across assigned oncology studies

Work with industry leaders and subject matter experts.

Opportunity to mentor junior CRAs.

Work with world-class technology.

Great opportunities to travel, work from home, meet new people and play a pivotal role in the drug development process.

Qualifications

Here are a few requirements specific to this advertised role.

Substantial Site Management experience, with an understanding of clinical trials methodology and terminology.

Experience monitoring or willingness to monitor oncology clinical trials.

Experience in independent monitoring, all types of visits.

Effective time management, organizational and interpersonal skills & problem-solving skills, with the ability to multi-task and prioritize.

Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines.

Apply Now

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