Enable job alerts via email!

Senior Medical Director, Medical Affairs (Oncologist) - U.S. Remote

Worldwide Clinical Trials Holdings, Inc.

North Carolina

Remote

USD 120,000 - 180,000

Full time

30+ days ago

Boost your interview chances

Create a job specific, tailored resume for higher success rate.

Job summary

Join a pioneering global CRO as a Senior Medical Director in Medical Affairs, specializing in Oncology. This role offers the chance to influence clinical investigations from inception to regulatory submission while collaborating with diverse teams. You'll provide vital medical insights, mentor staff, and engage in impactful projects that improve patient lives. With a commitment to innovation and quality, this forward-thinking company fosters an inclusive environment where your expertise can shine. If you're passionate about making a difference in the healthcare landscape, this opportunity is tailored for you.

Qualifications

  • 3-5 years of medical monitoring experience in a CRO is preferred.
  • Board certification in Oncology is required.

Responsibilities

  • Contribute medical input into clinical development programs and study protocols.
  • Assist in the preparation of study reports and documentation.

Skills

Medical Monitoring
Organizational Skills
Time Management
Presentation Skills
Excellent English Communication

Education

Medical Degree with Oncology Focus

Tools

Microsoft Word
Microsoft Excel
Microsoft Access

Job description

Senior Medical Director, Medical Affairs (Oncologist) - U.S. Remote

Who we are

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!

What Medical Affairs does at Worldwide Clinical Trials

Medical Affairs plays a pivotal role throughout the entire life cycle of a clinical investigation, exerting its influence from the initial stages of Business Development to the final Regulatory Submissions. Within this multifaceted domain, the dedicated members of the Medical Affairs team provide essential support to the broader project team, contributing to the cultivation of the scientific and medical principles that define Worldwide's philosophy.

Collaboration is a cornerstone of Medical Affairs, as you work closely with other functional groups within the Worldwide organization. As a member of our team, you will have the opportunity to engage in the entire spectrum of clinical investigation activities, from initial database construction to the final delivery of project datasets.

Within Medical Affairs, you will discover a diverse range of roles, including direct interactions with pharmaceutical companies, protocol preparation, feasibility assessments, training of site staff, medical monitoring, pharmacovigilance, and medical writing. These roles present ample opportunities for you to excel and contribute your unique talents to our mission to impact millions of patients' lives around the globe!

What you will do

  • Contributes medical input into the design of clinical development programs, study protocols, research papers, client-focused white papers, etc.
  • As directed supports Business Development through participation in proposal generation, feasibility assessments, review of proposals/contracts for medical services, and attendance at meetings with sponsors as directed by department senior management.
  • Reviews and/or assists in the preparation of final study reports (CSRs), or other study documentation (Protocols, ISS/ISEs etc.) as directed by senior management.
  • Maintains a high level of competence with assigned projects, including knowledge of project and therapeutic advances as well as marketplace developments by participating in internal meetings (company-wide project tracking, medical management meeting, etc.), review of relevant therapeutic/clinical literature, and attendance in conferences and meetings.
  • Assists in the mentoring of other medical staff as directed by Senior Management and by consistently displaying exemplary work ethics, compassion, and integrity, supports Senior Management’s leadership of both the department and the company.

What you will bring to the role

  • Excellent computer skills (Word, Excel, Access).
  • Excellent spoken and written English skills.
  • Excellent organizational and time management skills.
  • Excellent presentation skills.

Your experience

  • Medical Degree from an accredited institution of Medical Education with an Oncology focus (board certification required).
  • At least 3 - 5 years of medical monitoring experience, preferably in a CRO.
  • Candidates living in the U.S. Eastern or Central Time Zones strongly preferred.
  • Valid passport and ability to travel as required up to 20%.

We love knowing that someone is going to have a better life because of the work we do.

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.

Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.

Similar jobs

Senior Medical Director, Medical Affairs (Oncologist) - U.S. Remote

Worldwide Clinical Trials - USA

North Carolina

Remote

USD 150,000 - 210,000

30 days ago

Vice President, Medical Affairs - Endocrinology - U.S. Remote

Worldwide Clinical Trials - USA

Durham

Remote

USD 90,000 - 150,000

30+ days ago