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Weekend Ppd Clinical Research Jobs (NOW HIRING)

$150 - $230/hr

No nights, weekends, or on-call responsibilities * Research-focused role with meaningful patient ... Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple ...

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Weekend Ppd Clinical Research information

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How much do weekend ppd clinical research jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for weekend ppd clinical research in the United States is $22.71, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $25.96 per hour, depending on experience, location, and employer.

What is a Weekend PPD Clinical Research?

A Weekend PPD Clinical Research job involves working primarily on weekends to support clinical research studies managed by PPD, a leading global contract research organization. Employees in this role may assist with tasks such as data collection, patient recruitment, study monitoring, and ensuring compliance with research protocols. This position is ideal for individuals seeking flexible work schedules while contributing to important medical research. Weekend roles are essential for studies that require continuous monitoring or have participants available only outside regular business hours.

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

To thrive as a Weekend PPD Clinical Research professional, you need a background in life sciences or healthcare, experience in clinical trial processes, and often a relevant degree or certification such as GCP (Good Clinical Practice). Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and regulatory documentation is essential for the role. Strong attention to detail, effective communication, and organizational skills set top candidates apart in managing protocol adherence and patient safety. These skills and qualifications ensure high-quality clinical data integrity, compliance with regulations, and smooth trial operations during weekend shifts.

What are some unique challenges and expectations faced by Weekend PPD Clinical Research staff compared to weekday roles?

Weekend PPD Clinical Research staff often work with reduced onsite support and may need to take on a broader range of responsibilities, such as patient monitoring, data entry, and protocol compliance independently. The pace can be variable, with periods of high activity when studies are scheduled and quieter intervals between participant visits. Strong communication skills are essential, as coordination with weekday teams ensures seamless handovers and continuity of care. This role offers valuable experience managing complex clinical tasks autonomously and is ideal for professionals seeking flexible schedules or additional clinical research exposure.

What is the difference between Weekend Ppd Clinical Research vs Clinical Research Coordinator?

AspectWeekend Ppd Clinical ResearchClinical Research Coordinator
CertificationsTypically requires GCP training, CPR, and sometimes clinical research certificationsOften requires GCP training, CPR, and research certifications
Work EnvironmentPart-time, weekend shifts at clinical sites or research facilitiesFull-time or part-time roles at research sites, hospitals, or clinics
Employer & IndustryPharmaceutical companies, CROs, research sitesHospitals, research institutions, pharmaceutical companies

Weekend Ppd Clinical Research roles focus on conducting research activities during weekends, often part-time, while Clinical Research Coordinators manage daily study operations, patient recruitment, and data collection. Both roles require similar certifications but differ mainly in schedule and scope of responsibilities.

What cities are hiring for Weekend Ppd Clinical Research jobs?

Cities with the most Weekend 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 Weekend Ppd Clinical Research jobs?

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

ED/VP Medical Science & Strategy - Oncology

Thermo Fisher Scientific

Cornelius, NC • On-site

Full-time

Posted 12 days ago


Thermo Fisher Scientific rating

7.8

Company rating: 7.8 out of 10

Based on 429 frontline employees who took The Breakroom Quiz

170th of 545 rated manufacturers


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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