Parexel Clinical Research Associate Job For Biological Sciences

Parexel Clinical Research Associate Job For Biological Sciences

Parexel Clinical Research Associate Job For Biological Sciences. Life Science, Biological Sciences Clinical Research Associate II Jobs. Parexel Clinical Research Associate II Biological Science career. Parexel has job openings for biological sciences candidates. Check out all of the details on the same below:

Parexel Vacancy Details

Designation: Clinical Research Associate II

Requisition ID: 70024411

Location: INDIA – ANY REGION – HOME BASED

Your time here:

At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA’s are accountable for utilizing their expertise to build and also maintain the site relationship and guarantee they’re set up for success. As the clinical sites’ sole point of getting in touch with, this consists of addressing as well as dealing with site issues and also questions. You’ll also manage site quality as well as delivery from site identification through to close-out.

As a CRA, Parexel will certainly offer you world-class technology and also training catered to your individual experience. You can anticipate less travel and a lower protocol load in comparison to industry peers. Your hard work may be rewarded via a bonus incentive program, the opportunity to

work within multiple therapeutic areas and an opportunity to advance your career in clinical research. If impact, flexibility, and career development appeal to you, Parexel could be your next home.

What you’ll do:

• Leverage your expertise. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) as well as termination visits (TV) at assigned clinical sites and generate visit/contact reports.
• Build relationships. Oversee integrity of the study as well as use problem-solving abilities to promote rapport with the site as well as staff.
• Protect patients. Review the performance of the trial at designated sites, guarantee the rights and well-being of human subjects are safeguarded and are in accordance with the protocol.
• Drive productivity. Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines, while additionally guaranteeing compliance with the approved standard operating procedures (SOPs), protocol/amendment( s), GCP, and also the applicable regulatory requirement( s).
• Ensure quality. Evaluate the quality and integrity of the reported data, site efficacy as well as drug accountability.
• Execute. Monitor the completeness and also the quality of Regulatory Documentation as well as perform site document verification.

More regarding you:

On your first day we’ll expect you to have:

• Site Management or equivalent experience in clinical research, with an understanding of clinical trials methodology as well as terminology.
• Ability to perform all clinical monitoring activities independently.
• Bachelor’s or equivalent degree in biological science, pharmacy or various other health-related disciplines.
• Strong interpersonal, written, and verbal communication abilities within a matrixed team.
• Experience working in a self-driven capacity, with a sense of urgency and limited oversight.
• A client-focused approach to work and a flexible attitude with respect to assignments/new learning.
• The ability to manage multiple tasks, evaluate a variety of unpredictable scenarios and achieve project timelines while being able to apply your understanding of study protocol(s).
• An honest and also ethical work approach to promote the development of life-changing treatments for patients.
• Strong computer abilities, including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS) and also MS-Office products such as Excel and also Word.

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