Study manager (FSP )

Posted Yesterday
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Shanghai, Shanghai Municipality, Shanghai, CHN
In-Office
Senior level
Pharmaceutical
The Role
Manage clinical studies, ensuring quality and timelines while engaging with site staff. Identify risks and comply with regulatory standards.
Summary Generated by Built In

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.

Key Accountabilities: 

General Accountabilities 

  • Build and maintain engagement with Investigators, other site staff  in collaboration with other functions, to ensure trial speed and effective start up, conduct and close out. 

  • Ability to manage studies and processes to agreed quality and timelines. 

  • Ability to proactively identify & mitigate risks around study/site level in study execution. 

  • Knowledge of the clinical development process, understand concepts and principles of study design, and application to manage and run studies. 

 

Compliance with Parexel standards  

  • Comply with required training curriculum.  

  • Complete timesheets accurately as required.  

  • Submit expense reports as required.  

  • Update CV as required.  

  • Maintain a working knowledge of and comply with Parexel processes, ICH-GCPs and other applicable requirements.  

  • Previous experience in scientific and/or regulatory medical writing. 

  • Strong Communication Skills 

Knowledge and Experience:  

  • Keen problem-solving skills. 

  • Fluent in both oral and written English. 

  • Fluent in host country language required.  

  • At least 5 years in clinical practices 

Education: 

  • Minimum of BS/BA in a biomedical discipline or equivalent education/training is required 

Skills Required

  • At least 5 years in clinical practices
  • Fluent in both oral and written English
  • Minimum of BS/BA in a biomedical discipline or equivalent education/training
  • Previous experience in scientific and/or regulatory medical writing
  • Strong communication skills

Parexel Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Parexel and has not been reviewed or approved by Parexel.

  • Healthcare Strength Health coverage is described as comprehensive, including medical, dental, vision, HSA/FSA options, and company-paid disability insurance. Descriptions often portray the package as strong or “top notch,” adding meaningful value.
  • Retirement Support Retirement offerings include a 401(k) with company matching and, in some regions, generous pension contributions. Core financial protections are emphasized as a solid part of the total rewards.
  • Leave & Time Off Breadth Time-off programs include ample PTO or flexible/unlimited RTO alongside flexible schedules and remote/hybrid options. Work-life balance support from managers is highlighted as a practical advantage.

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The Company
HQ: Durham, North Carolina
20,524 Employees

What We Do

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.

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