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Weekend Ppd Clinical Research Jobs (NOW HIRING)

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Clinical Research Coordinator (Onsite) Dallas, TX Contract Role Ready to make an impact in medical ... Enjoy a steady weekday schedule --no weekends or holidays * Gain hands-on experience with industry ...

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Clinical Research Coordinator (Onsite) Dallas, TX Contract Role Ready to make an impact in medical ... Enjoy a steady weekday schedule --no weekends or holidays * Gain hands-on experience with industry ...

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Clinical Research Coordinator (Onsite) Dallas, TX Contract Role Ready to make an impact in medical ... Enjoy a steady weekday schedule --no weekends or holidays * Gain hands-on experience with industry ...

Showing results 21-40

Weekend Ppd Clinical Research information

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$8

$22

$46

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

As of Aug 17, 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 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 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 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 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:

Group Leader - Bioanalytical LCMS Research and Development

Thermo Fisher Scientific

Richmond, VA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 6 days ago


Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 427 frontline employees who took The Breakroom Quiz

199th of 540 rated manufacturers


Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
This is a fully onsite role based in our bioanalytical laboratory at 8700 Quioccasin Road in Richmond, VA. We welcome applicants from all locations within the US. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate.
Must be legally authorized to work in the United States without sponsorship.
Must be able to pass a comprehensive background check, which includes a drug screening.
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.
Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic experts. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations.
Discover Impactful Work:
Provides management and direction to laboratory staff and resources for project activities and needs, oversee daily operations to monitor quality and project timelines, and assist in preparation and implementation of company policies, quality systems and training programs. Ensures responsiveness to the customer and overall, client satisfaction. Plans and monitors the progress and quality of projects by utilizing the financial and quality management tools available at PPD.
A Day in the Life:
• Prepares, reviews and approves study protocols, project status reports, final
study reports and other project-related technical documents.
• Designs experimental study and participates in technical troubleshooting.
• Reviews data for technical quality and compliance to protocols, methods and
SOPs. Reviews and approves laboratory investigations, deviations, and QA facility and data audits. Leads client and FDA audits.
• Allocates, schedules and manages laboratory resources for group's project
activities and updates project status. Reviews timesheet reports for billing
accuracy.
• Responds to clients questions and needs; leads client technical meetings.
• Assists in preparation of proposals by provided project definition.
• Identifies new opportunities within client base and ability to work with business development to pursue opportunities.
• Coordinates and prioritizes project activities with internal functional groups
(physical testing, analytical development, microbiology, etc.) and support
functions (QA, sample management, etc.).
• Assists management in their responsibilities.
• Prepares and implements PPD SOPs and company operational policies. Ensures adherence and makes recommendations to quality system improvements.
Keys to Success:
BS Degree + 8 years of experience (must include 1+ year of management responsibility)
OR MS + 6 years of experience (must include 1+ year of management responsibility)
OR PhD + 3-5 years of experience (must include 1+ year of management responsibility)
In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills and Abilities:
• Proven leadership skills
• Ability to cultivate a collaborative work environment with a team
• Effective negotiating skills
• Demonstrated knowledge of QA metrics of program base; ability to write and recommend changes to PPD SOPs
• Ability to troubleshoot multiple systems/methodologies
• Ability to independently optimize analytical methods
• Understanding of basic financial terms and definitions as it applies to the business
• Understanding of proposal and project scope as it relates to pricing, resource management and the impact on business
• Project and time management skills
• Effective written and oral communication skills as well as presentation skills
• Ability to train and mentor junior staff
Work Environment:
Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:
  • Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
  • Able to work upright and stationary and/or standing for typical working hours.
  • Able to lift and move objects up to 25 pounds.
  • Able to work in non-traditional work environments.
  • Able to use and learn standard office equipment and technology with proficiency.
  • May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.
  • Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.

Compensation and Benefits
The salary range estimated for this position based in Virginia is $100,000.00-$115,000.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
  • A choice of national medical and dental plans, and a national vision plan, including health incentive programs
  • Employee assistance and family support programs, including commuter benefits and tuition reimbursement
  • At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
  • Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
  • Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

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