Job type full-time
Full job description
Sr investigator grants manager - (22004185) description
Senior investigator grants manager
Come discover what our 25,000+ employees already know: work here matters everywhereWe’re a growing and evolving biopharmaceutical industry leader, which means you’ll have endless opportunities to work with experts around the world and build the career you’ve dreamed of.
As a part of the syneos health team, you’ll help us deliver results for a rewarding reason – we improve patients’ lives around the worldBecause to us, a patient isn’t just a number, they’re our family, friends, and neighbors.
Why syneos health
#syneoshealthlife means we’re committed to our total self culture – where everyone can authentically be themselvesOur total self culture is what unites us globally, and we know every person’s unique contributions make a difference.
We believe our success is a direct result of the people who are driving it – you! we value your dedication to care for our customers and patients, so we want to focus on taking care of youThat’s why we offer a comprehensive benefits program encompassing your total health - physical, mental and financial.
We are continuously building the company we all want to work for and our customers want to work withWhy? 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.
Receives and analyzes rfps documents with particular focus on protocol/synopsis details as they relate to determination of anticipated investigational study site and subject reimbursement costs.
Reviews and extracts details from rfp documents (clinical trial protocols/synopsis) related to site performed study activities and applies these to detailed investigator grant estimates.
Develops the detailed investigator grant budget estimates and supporting documents with assistance from clinical operations according to protocol specifications through currently available software package/resources.
Ensures investigator grants are in agreement with rfp, client specifications and communications, and internal assumptions.
Collaborates with team members, operations and business development, to ensure grants estimates are appropriate for the study.
Validates investigator grant estimates against available internal and external benchmarking data.
Tracks and measures progress through collection of cycle time metrics and other quality key performance indicators (kpis).
Updates proposals tools, systems and/or forms regarding proposal or rebid status and investigator grants value as directed.
Researches, compiles, and creates necessary information as required in support of generation of investigator grants.
Escalates issues/concerns to department leadership.
Serves as a subject matter expert (sme) resource to proposals/rfis, business development, and internal functions.
Ensures investigator grants tracking systems and tools are updated and current.
Explains roles/responsibilities and coaches project teams through grants generation process and system navigation, as needed.
Trains and mentors less experienced staff members on departmental standard operating procedures (sops), processes, tools, and templates, and ensures quality of teamwork products.
Actively participates in discussions about overall company goals, departmental objectives, and specific project aims.
Leads investigator grants projects that impact customer deliverables or provide efficiencies to the team.
Reviews metrics and process reporting regularly to determine if there are issues that require attention.
Identifies best practices, investigates root causes of fundamental issues and problems for projects, and recommends solutionsRecognizes and develops opportunities for continuous process improvement within investigator grants generation which lead to greater efficiencies and/or industry leading best practices.
What we’re looking for
Ba/bs degree or equivalent in a health related field, or equivalent combination of education and experience; plus some experience working in the cro/pharmaceutical industry.
Clinical trial expertise, experience in a healthcare related field (study coordinator, cra, nursing, healthcare administration) across multiple therapeutic areas preferredUnderstanding of the clinical trial process and involvement of cros.
Intermediate proficiency in microsoft office suite (word, excel, and powerpoint), email, and voicemail.
Above-average attention to detail, excellent oral/written communication skills along with highly-developed interpersonal and strong team oriented skillsAbility to work independently to meet deadlines.
Get to know syneos health
We are the only full-service biopharmaceutical solutions company in the worldThat means we bring together the best clinical and commercial minds to create a better, smarter, faster way to get medicines into the hands of patients who need it mostLearn more about syneos health.
Tasks, duties, and responsibilities as listed in this job description are not exhaustiveThe company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilitiesEquivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the job descriptionThe company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described aboveFurther, nothing contained herein should be construed to create an employment contractOccasionally, required skills/experiences for jobs are expressed in brief termsAny 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 employeesThe 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.
Primary location: north america - us home-based
Other locations: north america - usa-new-york-200-vesey-street, north america - usa-nc-morrisville-1030-syncst, north america - usa-wstrvle-500-worthington-rd
Job: site operations
Employee status: regular
Posted 1 day ago