Offer summary

Qualifications:

Minimum 5 years of experience in the Data Acquisition domain., Expertise in handling non-CRF activities and autonomous work on non-CRF data strategy., In-depth understanding of data management conventions and drug development processes., Experience with study conventions and knowledge sharing on non-CRF data standards..

Key responsibilities:

Lead the collection of non-CRF data during study setup, conduct, and closeout activities.

Communicate non-CRF data collection deliverables and status of work to the study team and SMEs.

Collaborate with multiple non-CRF vendors to set up Data Transfer Agreements.

Influence study teams to adhere to non-CRF guidance and negotiate contingency plans.

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com. Community Guidelines Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are: • Abusive, harassing or threatening to others. • Defamatory, offensive, obscene, vulgar or depicting violence. • Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs. • Sexually explicit or pornographic. • Fraudulent, deceptive, libelous, misleading or unlawful. • Referencing criminal or illegal activity. • Spamming. We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.

Job description

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Skills:

Min 5 yrs of experience in Data Acquisition domain.

Expertise in Handling Non-CRF activities, able to work autonomously on the non-CRF data strategy.
In-depth understanding of Data Management conventions, data standards, Processes and Drug development Process.
Experience with Study convention including non-CRF collection data standards, Processes, Knowledge sharing and best practices on assigned studies.
Influence Study Team to adhere non-CRF guidance, processes and negotiate contingency plans to mitigate delays of deliverables.

Task:

Lead collection of non-CRF data during Study Setup, Conduct and Closeout activities IXRS and Complex Data Models.
Effectively communicate non-CRF data collection deliverable, Status of work and Data issues to the assigned study team and SME’s.
Collaborate with multiple non-CRf vendors or data providers to setup Data Transfer Agreement to ensure timely and quality delivery.

Required profile