Clinical Project Manager - Biomarker Study Management Experience required (Sponsor Dedicated - US Re
Syneos Health, Inc.
Clinical Project Manager - Biomarker Study Management Experience required (Sponsor Dedicated - US Remote; Preference for Hybrid Foster City, CA) Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know:
WORK HERE MATTERS EVERYWHERE
We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to our Total Self culture - where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we're able to create a place where everyone feels like they belong. Job Responsibilities Clinical Project Manager II - Biomarker Study ManagementSponsor-Dedicated | Remote (Preference for Hybrid Foster City, CA-Based Candidates) We're hiring a Clinical Project Manager II with a strong background in biomarker study operations to join our sponsor-dedicated team. This fully remote role gives you the opportunity to drive the success of global clinical trials by leading biomarker and bioanalytical strategy from start to finish. You'll be a key player in bringing together cross-functional teams, vendors, and internal stakeholders to ensure biological samples are collected, managed, and analyzed to the highest standards. While remote/home-based candidates may be considered, priority will be given to candidates located within 50 miles Foster City, California, with the ability to work onsite 2-3 days per week.WHAT YOU WILL DO
Lead Biomarker Study Operations Oversee biomarker and bioanalytical activities across Sponsor and Collaborative programs Serve as the operational point of contact for all biomarker-related processes Work closely with clinical study teams (Phases 1-4) to integrate biomarker strategies into broader clinical development plans Plan and manage the collection, tracking, and analysis of biological specimens Advise study teams on best practices for sample management and logistics If you're passionate about clinical research and want to make a direct impact on advancing biomarker science with your expertise, we'd love to hear from you. ** Candidates without direct experience supporting Biomarker clinical trials can not be considered. **WHY JOIN US
Meaningful Work: Your contributions will directly support critical biomarker research that shapes the future of clinical development and precision medicine. Global Impact: You'll be working on high-profile studies that span multiple regions, making a real difference in patients' lives around the world. Dedicated Team: Join a collaborative, sponsor-dedicated environment where your expertise is trusted, and your voice matters. Professional Growth: Be part of a company that invests in your career through continued learning, mentorship, and leadership opportunities. Stability and Vision: Work with a leading global organization known for operational excellence and long-term partnerships in clinical research.SKILLS AND EXPERIENCE YOU BRING
Significant experience managing biomarker studies and external vendors required! Strong understanding of biomarker and bioanalytical strategies in a clinical trial setting Proven ability to coordinate complex sample collection and analysis workflows Expertise in supporting study teams with sample logistics and operational planning Bachelor's degree in Life Sciences, Medicine, Pharmacy, Nursing, or equivalent combination of education and experience Experience in a clinical research organization (CRO) or sponsor environment preferred Familiarity with GCP, ICH guidelines, and global regulatory standards Strong project management, organizational, and communication skills Comfortable working independently and embracing new technologies Willingness to travel up to 25% as needed Ensure Operational Excellence Maintain high-quality documentation, including Trial Master File (TMF) accuracy and completeness Keep study systems and databases current and audit-ready Prepare project reports and updates for sponsors and internal stakeholders Plan and facilitate internal and external meetings Support inspection readiness and regulatory compliance throughout the project Drive Clinical Project Delivery Lead cross-functional teams through the full clinical trial lifecycle, from start-up to closeout Ensure studies stay on track with respect to timelines, budget, scope, and quality Act as the main liaison between the sponsor and study partners Monitor and manage project financials, ensuring fiscal responsibility Proactively identify and resolve operational issues and risks We are always excited to connect with great talent. This posting is intended for a [possible] upcoming opportunity rather than a live role. By expressing your interest, you'll be added to our talent pipeline and considered should this role become available. At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements. company car or car allowance Health benefits to include Medical, Dental and Vision Company match 401k eligibility to participate in Employee Stock Purchase Plan Eligibility to earn commissions/bonus based on company and individual performance flexible paid time off (PTO) and sick time Salary Range: The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate's qualifications, skills, competencies, and proficiency for the role. Get to know Syneos Health Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. No matter what your role is, you'll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health. Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job. #J-18808-Ljbffr Syneos Health, Inc.- Description Experienced Clinical Project Manager - Inflammation (Sponsor Dedicated/ Remote- US only) Syneos Health®... ...take ownership of a study from start-up through... ...protocol and study requirements Contribute to SOP development... ...You Bring Required Experience 3+ years of clinical...SuggestedRemote jobContract workInterim roleImmediate startFlexible hoursShift work
- Description Clinical Trial Manager - Full... ...but to make us easier to work... ...and we are dedicated to taking care... ...Reviews the study scope of work... ...the clinical project team (CRAs/CeMs... ...clinical experience, operational... ...and may be required to interact... ...dashboards, Sponsor Standard Operating...SuggestedContract workTemporary workImmediate startFlexible hours
- Medix is seeking a Clinical Study Coordinator in Sacramento, CA, to manage participant recruitment and consent under the... ...regulatory documents. The role requires collaboration across clinical and... ...event reporting, and supporting sponsor visits and audits, with hands-on...Suggested
$32.4 - $48.6 per hour
## Clinical Research Coordinator II -... ...based practice, experience, innovation,... ...resilience define us as leaders in... ...Program Manager (or local Hospital... ...(s) and study sponsor(s). This position... ...research regulatory requirements. Has a working... ...aspects of projects including all...SuggestedPart timeWork at officeLocal area- Participant Management: Recruits, screens, and enrolls eligible study subjects; obtains informed consent under the guidance... ...schedules participant visits, clinical procedures, and follow-up care from... ...adverse events, and facilitates sponsor monitoring visits and audits #J...Suggested
- Serve as primary contact for clinical trial testing, managing sponsor/client relationships and... ...teams Maintain study logs, metrics, and provide... ...secondary QC Train staff as required Qualifications AA or BS degree... .../study coordination experience (CRO, university, or medical...
$30 - $33 per hour
About Us: Flourish Research is where clinical trials thrive.Flourish Research... ...(depending on experience) ESSENTIAL JOB... ...and other study related information... ..., protocol requirements and GCPs. C. Obtain... ...within the sponsor’s timeline while... ...Lead I; Team Manager; Principal Investigator...Hourly payCasual workWork at officeMonday to FridayShift workNight shiftDay shift- ...physicians to offer clinical trials as a... ...Patient-Physician Experience in Clinical Research... .... You’ll help manage study activities, lead... ...complete protocol-required procedures and documentation... ...investigators, sponsors, CROs, and... ...alongside a team of dedicated professionals who...Full timeContract workFor contractorsWork at office
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$140k - $178k
The Senior/Clinical Trial Manager will be responsible... ...trials, from study start-up to... ...with regulatory requirements, GCP guidelines... ...-functional project activities (e.... ...Required Education, Experience, Skills, And... ...of CRO and sponsor-side experience... ...contact us. #J-18808-Ljbffr...Hourly payFull timeSummer workRemote workRelocation packageMonday to Friday$52 - $75 per hour
Job Description Clinical Research... ...on the years of experience Job Type: Direct... ...Coordinator - RN II to manage and coordinate... ..., and biologic studies across Phase I-... ...physicians, sponsors, and research teams... ...standards . Required Qualifications:... ...firms in the US by SIA. Our mission...Hourly payFull time- ...UCI Center for Clinical Research (CCR)... ...Research Manager and the Assistant... ...completion of research projects with human... ...with study patients in the... ...submission to study sponsors ensuring... ...incumbent will be required to work at both... ...and/or experience. A minimum of...Work experience placementWork at officeLocal area
- Reports to: Clinical Research Coordinator Lead Job Location... ...clinical research studies from startup to close... ...patient interest. Manage and perform clinical study... ...as well as sponsor/CRO and IRB regulations... ...Phlebotomy training and experience with pediatric blood drawing...Full time
- ...Sacramento is seeking a motivated Clinical Research Coordinator to conduct and... ...coordinator will organize and run clinical studies, recruit participants, manage study procedures, and ensure... ...will have phlebotomy training and experience with pediatric blood drawing. This...Full time
- ...treatment. As a multi-specialty clinical site our facilities... ...Coordinator will manage and conduct clinical research studies. Daily responsibilities... ...professionals, and research sponsors to facilitate trial operations... ...research coordination experience Strong working...Full time
$36.35 - $58.45 per hour
...will act as the clinical research coordinator for all projects in the Department... ...day-to-day management of clinical trials... ...be both industry-sponsored and investigator-initiated studies. The position requires the use of skills... ...and sufficient experience and demonstrated...Hourly payTemporary workWork at officeLocal areaShift work- ...supervision of the Clinical Research Manager (CRM) within the Clinical... ...protocol specific requirements, research procedures... ...as the liaison to sponsors, governing agencies... ...leading and managing pre-study site selection... ...structure Demonstrated experience in maintaining...Work experience placementWork at officeLocal area
- ...of California, Davis seeks a Clinical Research Coordinator for the... ...Department of Urologic Surgery to manage daily clinical trials, data... ...coordinating trials industry-sponsored and investigator-initiated,... ...occasional travel and overtime may be required. This 100% on-site role...
$43.69 - $70.25 per hour
...for the Senior Clinical Research... ...coordination and management of clinical research studies within the Department... ...staff, sponsors, contract research... ...research projects generated by the... ...compliance with requirements; provide... ...education and/or experience.. Minimum three...Hourly payContract workTemporary workCasual workLocal areaShift work- ...Center of Excellence. You will coordinate clinical research activities, recruit and screen subjects... ...maintaining regulatory files and data management. The role requires knowledge of FDA regulations, HIPAA, and GCP, plus experience with IRB submissions and communication...
$31 - $44.5 per hour
...and designing new clinical trials to advance... ...the IRB-approved study protocol and/or manual... ...upon individual experience / knowledge and the... ...pharmaceutical sponsor representatives to... ...documented Creates, manages, and maintains... ...Collects data as required by the protocol and...Full timeContract workPrivate practiceWork at officeLocal areaImmediate startFlexible hours- ...Davis Health is seeking an Assistant Clinical Research Coordinator in Internal Medicine: Cardiology to manage day-to-day clinical trials,... ...multidisciplinary CV unit. The position requires strong organizational and regulatory skills, experience in clinical trials, and the...
$30 - $32 per hour
...community physicians to offer clinical trials as a... ...Best Patient-Physician Experience in Clinical Research... ...hands-on experience in study coordination, patient... ...benefit package. Physical Requirements & Work Environment... ...llwork alongside a team of dedicated professionals who are...Full timeContract workFor contractorsWork at office$52 - $75 per hour
LanceSoft is seeking a Clinical Research Coordinator - RN... ...in Newport Beach, CA to manage and coordinate complex clinical... ...phases I-IV. The role requires collaboration with physicians, sponsors, and research teams to... ..., and IRB documentation experience. #J-18808-Ljbffr...Hourly payFull time$55.15 - $70.62 per hour
...external hires that meet required qualifications and... ...of the Department Manager/Director, the Lead... ...technically and/or clinically competent,... ...Association 2 years of experience as a hospital-based... ...believe diversity makes us stronger, so we are dedicated to shaping an...Full timeLocal areaShift workDay shift- ...cardiovascular medicine clinical trials and research projects with a focus on... ...projects. Studies are conducted... ...collection and management, study audits... ...specimen processing, sponsor communications,... ...program as required, such as attend... ...or sufficient experience and...Contract workWork at officeNight shift
$32.95 - $53.06 per hour
...of the assistant clinical research coordinators... ...for research projects in Internal Medicine... ...day-to-day management of clinical trials... ...department. The position requires the use of skills... ...of clinical studies. The clinical... ...and/or sufficient experiance and demonstrated...Hourly payFull timeContract workTemporary workPart timeWork at officeLocal areaRemote workMonday to FridayShift work- ...Assistant Research Data Coordinator to support data management for cancer trials at the Chao Family... ...ensuring accuracy, regulatory compliance, and timely sponsor submissions. You will collaborate with clinicians and study staff, maintain trial data in OnCore, and assist...
- UC Davis Health seeks an assistant clinical research coordinator for Internal Medicine: Cardiology. You will help manage day-to-day clinical trials, focusing on data management and regulatory duties within the cardiovascular clinic, including on-call responsibilities. The...Part time
$175k - $200k
The Associate Director, Clinical Operations will be responsible for managing operational aspects of assigned... ...on early-phase oncology studies. This includes oversight... ...regions. The role requires a deep understanding of... ...phase oncology trials at a sponsor biotech. Essential...Full timeContract workSummer workRelocation packageMonday to Friday
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