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Evening Ppd Clinical Research Jobs (NOW HIRING)

Clinical Research Coordinator

Stanford, CA · On-site

$28.50 - $38/hr

As a Clinical Research Coordinator, you will oversee complex aspects of multiple studies under the ... Occasional evening and weekend hours may be necessary. Due to the number of candidates, we kindly ...

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Evening Ppd Clinical Research information

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$49K

$107.3K

$189K

How much do evening ppd clinical research jobs pay per year?

As of Aug 31, 2026, the average yearly pay for evening ppd clinical research in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What is an evening PPD Clinical Research position?

An Evening PPD Clinical Research position involves working with a clinical research organization, like PPD (Pharmaceutical Product Development), during evening hours to support clinical trials. Responsibilities often include collecting data, monitoring patients, ensuring compliance with protocols, and assisting with study documentation. These roles are essential for ensuring that research studies are conducted accurately and safely outside of standard business hours. Candidates usually need a background in healthcare or life sciences and must be detail-oriented with excellent organizational skills.

What are the key skills and qualifications needed to thrive as an evening PPD Clinical Research professional?

To thrive as an Evening PPD Clinical Research professional, you need a background in life sciences, clinical trial protocols, and experience with regulatory compliance, often supported by a relevant degree or certification such as GCP (Good Clinical Practice). Familiarity with clinical data management systems, laboratory technology, and electronic data capture (EDC) platforms is commonly required. Strong attention to detail, effective communication, and adaptability to evening shifts are essential soft skills. These abilities ensure accurate data collection, regulatory adherence, and smooth collaboration during non-standard hours in clinical research environments.

What are some common challenges faced by clinical research professionals working evening shifts, and how can they be managed?

Clinical Research professionals working evening shifts may encounter challenges such as limited access to daytime support staff, coordinating with teams working standard hours, and maintaining consistent communication with participants and colleagues. To manage these challenges, it's important to establish clear communication protocols, leverage digital collaboration tools, and schedule regular check-ins with daytime teams. Additionally, maintaining a structured routine and prioritizing self-care can help ensure both productivity and well-being during evening hours.

What is the difference between Evening Ppd Clinical Research vs Evening Ppd Clinical Trial Coordinator?

AspectEvening Ppd Clinical ResearchEvening Ppd Clinical Trial Coordinator
CertificationsGCP training, clinical research certificationsGCP training, clinical research certifications
Work EnvironmentResearch facilities, labs, clinical sitesResearch facilities, clinical sites
Employer & IndustryPharmaceutical companies, CROs, research institutionsPharmaceutical companies, CROs, research institutions

Both roles involve supporting clinical trials, requiring similar certifications and working in research environments. The main difference is that Evening Ppd Clinical Research may focus more on data collection and regulatory compliance, while Evening Ppd Clinical Trial Coordinators often handle patient scheduling and trial logistics. Understanding these distinctions helps candidates choose the right role based on their skills and career goals.

What cities are hiring for Evening Ppd Clinical Research jobs?

Cities with the most Evening Ppd Clinical Research job openings:

What are the most commonly searched types of Ppd Clinical Research jobs?

The most popular types of Ppd Clinical Research jobs are:

What states have the most Evening Ppd Clinical Research jobs?

States with the most job openings for Evening Ppd Clinical Research jobs include:

ED/VP Medical Science & Strategy - Oncology

Cornelius, NC • On-site


Thermo Fisher Scientific
Biotechnology Research and Development • 10K+ employees

7.8

Company rating: 7.8 out of 10

Based on 429 frontline employees who took The Breakroom Quiz

170th of 545 rated manufacturers

People enjoy working here

Good employer

Recommended by students


Full-time

Posted 6 days ago


Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

We seek an Executive Director/Vice President for our Medical Science and Strategy Team - Oncology.

The role can be based in the EMEA region but will require travel to China (or relocation could be considered).

The position requires proven abilities to drive both strategic and measurable business outcomes. The incumbent’s Oncology track record expertise is required to be extensive and ensure recognition as peer of their Pharmaceutical Industry equivalents. This position is playing a key part in the future success of the PPD clinical research business of Thermo Fisher Scientific, as it seeks to continue its track record of successful growth and expand Industry leading position in Oncology. Medical Science & Strategy physicians are subject matter experts who support sales for proposals and bid defences, engaging clients senior medical / scientific leadership in discussions and training internal staff on medical and therapeutic requirements of the proposals.

The role comprises four major functions:

  • First, the incumbent is responsible for ensuring the highest possible quality of input into significant requests for proposals (RFPs), including:

    • Development strategy and regulatory issues

    • Drug class issues

    • Protocol and indication considerations, including safety

    • Team education on indication

    • Interactions with client’s physicians and / or client area indication leaders prior to and during bid defences

    • Identifying business opportunities for the PPD clinical research business

  • Secondly, the incumbent is responsible for supporting outstanding input into other areas of the PPD clinical research business activities, including:

    • Pro-active client engagement: peer-to-peer interactions with therapeutic area leaders and senior directors of companies whose portfolio contains drugs of business interest

    • Strategic alliance development & support

    • Client governance and advisory boards

    • Through PPD’s consulting practice, the incumbent will provide Industry gold standard product development plans, and top-level design of clinical trial protocols that are required in the development plan.

  • Thirdly, the incumbent will be responsible for providing therapeutic and developmental expertise to internal teams, including:

    • Indication specific training for clinical teams

    • Guidance during clinical trials executions

    • Investigator Brochure, clinical study report, NDA / MAA clinical packages development, and other regulatory briefing documents authoring and review

    • Contribute to design and reporting of feasibility studies

    • Liaise with investigators and KOLs

    • Mentor and supervise clinical scientists

  • Finally, the incumbent will participate in multidisciplinary teams and working groups to contribute to innovative initiatives based on their specific knowledge, expertise and interest.

Minimum Qualifications:

  • MD or equivalent required

  • Certified Oncologist with at least 5+ years’ experience in pharmaceutical industry leading clinical development of at least one asset from discovery through registration.

  • Proficient in spoken and written English and Mandarin

  • Active medical license preferred but not required.

Knowledge, Skills and Abilities:

  • Able to work in a matrix organization.

  • Able to demonstrate the following key high-level high-performance behaviors: decisive, customer driven, flexible thinking, smart-risk taking and continuous improvement.

  • Leads, influences and motivates staff within and across departments.

  • Strong in presenting and communicating complex information clearly.

  • Able to deal with sensitive and confidential issues.

  • Possesses a “can do” attitude and is capable of implementing and following through on activities / projects.

  • Flexibility to travel domestically and internationally

What we offer:

  • Full time position

  • Competitive salary and benefits

  • Work diversity, exposure to several assets in different stages of clinical development from several clients

  • Mentorship and training

  • Exciting work environment

About the PPD clinical research business of Thermo Fisher Scientific: Our mission is to enable our customers to make the world healthier, cleaner and safer. As one team of 100,000+ colleagues, we share a common set of values – Integrity, Intensity, Innovation and Involvement – working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued. Apply today!



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