job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Internationally known for creating cutting-edge biopharmaceuticals for patients who live with rare genetic diseases, our partner strives to develop critical therapies for the small population - mostly children - that suffer from near unheard of conditions. If you're looking for an exciting opportunity to make a difference with an established company, this is the position for you! Remote - Territory will be focused in the South East/South Central (includes NC, SC, GA, FL, AL, MS, TX and may include additional). Candidate to be based in US, location flexible. PR - $76-89/hr location: Novato, California job type: Contract salary: $76.32 - 89.79 per hour work hours: 9 to 5 education: Bachelors responsibilities: RESPONSIBILITIES INCLUDE: Execute PKU medical MSL plan and tactics within assigned territory to meet scientific objectives and company-defined goals for products both marketed and in developmentProvide education relative to disease state, and products across the PKU product lifecycle to health care providers, dietitians, genetic counselors, researchers and other healthcare team membersServe as a medical/scientific resource through answering unsolicited medical questions and addressing other related medical information issuesEngage in scientific exchange and provide feedback on emerging clinical/competitive trends Identify, document, discuss and communicate insights to internal stakeholdersMaintain clinical and technical expertise in relevant therapeutic areaPartner with medical and research and compliantly collaborate with commercial Provide support to PKU clinical trials including but not limited to the following: site evaluation and identification; recruitment; investigator meetings; external expert identification; and study managementSupport the clinical department by communicating potential investigators for other products in developmentSupport the implementation and coordination of external investigator-initiated researchParticipate in local, regional, and national meetings/conferences in support of all scientific and medical objectivesAssist in the site level management of the publication plan timelinesWork with internal Medical Affairs partners to develop and execute a territory plan designed to support and meet strategic medical objectivesInput to and maintain internal documentationReview scientific journals, lead and participate in internal journal clubsServe as a scientific resource to commercial and marketing partners. Participate in sales team training, medical updates, scientific presentations, journal clubs, and other approved meetingsHave responsibility for assigned special projects and mentoring of other team members Self-development: Develops and communicates a professional growth plan. Takes responsibility for and actively manages professional development. Continually educates self on global market issues, trends, and product knowledge as it pertains to specific business responsibilities in key therapeutic areasAssure compliance with operational guidelines qualifications: Required Skills and Qualifications BA/BS in life or health sciences5 or more years of relevant clinical/industry experienceMedical Science Liaison or MSLKnowledge of regulations impacting Medical Affairs and field activities in the pharmaceutical industryExcellent oral and written communication, organization, and interpersonal skillsProven track record as a team playerProject management/leadership experienceAbility to work in a virtual environmentPosition will require 40-60% field travel for field and home office obligations. Travel may be variable dependent on COVID restrictions. Preferred Skills: 3 or more years as Medical Science Liaison or MSL is preferredExperience in rare genetic diseases/PKU preferredExperience in product launch, development, and execution preferredAdvanced degree (MS, doctoral level) preferred skills: Medical science liaison, Medical Information Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. Qualified applicants in the unincorporated areas of Los Angeles County with criminal histories will be considered for employment in accordance with the Los Angeles County's Fair Chance Ordinance for Employers. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.