Logo for Parexel

Scientific Leadership Research Coordinator

Role overview

Qualifications

  • 2+ years of pharmaceutical or healthcare-related experience
  • Strong leadership, project management, and organizational awareness skills
  • Resilience, collaborative and interpersonal skills
  • Research database proficiency

Responsibilities

  • Contributes within the specific Therapeutic Area (TA) and interacts with a continuum of stakeholders
  • Ensure meaningful and collaborative scientific exchange through engagement activities
  • Manage operations of client’s Investigator Studies Program
  • Manage Congress Operations activity for the TA

Key facts

  • Remote from: United States
  • Full time
  • Mid-level (2-5 years)
  • Clinical Research Coordinator
  • English

Hard skills

Other skills

  • Leadership
  • Organizational Awareness
  • Social Skills
  • Microsoft Office
  • Collaboration
  • Resilience

About the company

Parexel logo

Parexel

Contract Research Organizations (CRO)

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.

Company details

Company typeXLarge
IndustryContract Research Organizations (CRO)
Company size10001

Your match analysis

See how your profile stacks up against this role.

We compared the job requirements to your profile to show where you're strong and where you fall short.

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.

Parexel FSP has an exciting opportunity for a candidate with project management skills and a strong science background! This is a remote role with occasional travel.


Description of Roles and Responsibilities

• Contributes within the specific Therapeutic Area (TA) and interacts with a continuum of stakeholders.

• The SLRC is required to ensure that meaningful and collaborative scientific exchange through engagement activities is achieved to globally impact our strategies.

• Key to the role is the optimal management of the operations of client’s Investigator Studies Program

• The SLRC manages Congress Operations activity for the TA.


Project Management

• Congress support for the TA

• These key functions contribute to the development and refinement of our TA Scientific and Medical Affairs Strategic Plan for Our Company Research Laboratories.

• Ensures that the oversite of these activities is achieved to globally impact the scientific strategy for TA



Minimum FTE Years of Experience

• 2+ years of pharmaceutical or healthcare-related experience in internal or external scientific research operations

• Strong leadership, project management, and organizational awareness skills

• Resilience, collaborative and interpersonal skills

• Ability to coordinate across divisions

• Ability to lead without direct authority over a continuum of stakeholders

• Research database proficiency

• Experience with Microsoft Office applications


Educational Requirement

Bachelor's degree


#LI-KW1

EEO Disclaimer
Parexel is an equal opportunity employer.  Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

Apply once. Then go straight to the hiring manager.

After you apply, unlock the direct contact details of the people who actually make the call. A quick follow-up makes you 5x more likely to land an interview.

MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
Unlocked after you apply
·

Clinical Research Coordinator Related jobs

Other jobs at Parexel

Premium

Reach out to the hiring manager directly.

Gain access to the contact details of the hiring managers who actually decide, and reach out to network with them directly. That, plus more when you upgrade:

  • Full match report with fit score and gaps
  • Career diagnostics on how recruiters read you
  • Curated company matches and warm intros
  • 48h early access to new roles

Cancel anytime.