clinical case manager salaries in boston, massachusetts

job summary: Medical Monitor - MD | Rare Disease Trials 3 month contract | extension expected Are you an MD with a passion for clinical research and a desire to make a significant impact in a fast-paced biotech environment? Exciting opportunity for a Medical Monitor to shape clinical trials and engage directly with investigators while contributing to groundbreaking programs. MUST HAVE MD Degree ~5+ years of Clinical Research / Medical Monitoring experience Expertise in all core Medical Monitoring areas (see requirements) Experience working in smaller pharma or biotech settings TA Focus: Rare Disease, Autoimmune, GI, Endocrinology, Neuro Willing to travel 25-30%   location: Lexington, Massachusetts job type: Contract work hours: 9 to 5 education: Doctorate   responsibilities: Responsibilities: Evaluate Adverse Events (AEs) and Serious Adverse Events (SAEs). Respond to safety inquiries from study sites. Follow up with Principal Investigators (PIs). Perform data review. Settting up and participating/presenting in Data Monitoring Committees (DMCs) Managing safety vendors and interpret AEs. Facilitate site interactions, including protocol implementation and interpretation of inclusion/exclusion criteria. Collaborating with Clinical Operations to address logistical questions and issues from sites. Travel to sites and key conferences across Neuro, GI, and Endocrine therapeutic areas to meet PIs in person.  qualifications: Required Qualifications: Medical Doctor (MD) Degree 5 years of experience in clinical research in a Medical Monitoring capacity Experience working within a smaller pharma or biotech organization. Comfortable with a high expected amount of travel (25-30%). Experience with Data Monitoring Committees (DMCs), setup, participation, and presentation. Experience managing safety vendors and interpreting AEs. Strong site interaction skills, including protocol implementation, interpreting inclusion/exclusion criteria, and facilitating enrollment. Ability to work collaboratively with Clinical Operations teams to resolve site-related questions and issues. Board certifications not required *LI-AT1   skills: Clinical research, GCP (Good Clinical Practice), Drug Safety, ICH Regulations, AD (Adverse Events) 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: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (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.

Randstad is working with a premier firm in Downtown Boston, MA to join their medical case review team. This role will join a team of highly tenured individuals in a new position due to growth and influx of work. This company highly values work/life balance, is a human first environment, and has a Monday-Friday 9AM-5PM schedule. This is a fully onsite position in Downtown Boston, MA, and is an excellent way for a driven, highly attention and detail oriented professional to build their career in a high growth position. The ideal candidate will have experience and education in a medical/healthcare setting, a Bachelor's Degree, and a desire to get into a dynamic legal organization. Qualifications: -Bachelor's degree in biology, health sciences, or related; pre-health concentration a plus -Highly intelligent, analytic, and detail-oriented -Driven by completing tasks and checklists -strong attention to detail and computer skills  salary: $55,000 - $60,000 per yearshift: Firstwork hours: 9 AM - 5 PMeducation: BachelorsResponsibilities-Extract Key Clinical Information: Utilize structured checklists to precisely identify and flag vital clinical data from essential medical records (e.g., pathology, delivery, and operative notes). -Facilitate Medical Review for Court: Help prepare the medical review sections of court documents by digitizing scanned records for search ability and creating comprehensive tables of contents for easy navigation by nurse investigators. -Inform Case Strategy: Conduct focused medical research to provide critical support for ongoing case development. -Protect Sensitive Data: Carefully review medical records to redact confidential content.SkillsLegalData CollectionElectronic Health Records (EHR)MEDICAL MALPRACTICEmedical records (1 year of experience is preferred)QualificationsYears of experience: 1 yearExperience level: Entry LevelRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. 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: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (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.

job summary: The Functional Genomics group in the Target, Disease, and Systems Biology global function is seeking a collaborative and highly motivated research associate! This team is focused on generating scientific knowledge that translates into transformative therapies for patients with unmet medical need. Our multidisciplinary team works closely with diverse therapeutic area experts across immunology, ophthalmology, rare and neurological diseases, oncology, and gene therapy to identify and validate the next generation of groundbreaking therapeutics using CRISPR screens, automation, flow cytometry, and genomics. The successful candidate will contribute to drug target discovery projects for multiple indications and will gain deep training, knowledge and expertise in the application of cutting-edge technologies to drug development, including using CRISPR, siRNA, and pharmacological perturbations for target identification and validation.   location: Cambridge, Massachusetts job type: Contract salary: $44 - 45 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Summary of key responsibilities Independently run biological experiments, including analyzing resultsCollaborate with senior researchers to develop and execute existing and novel cell-based assays to identify, validate, and translate high-value targets in diverse clinical indicationsExplore, implement, and master new techniques and approachesCollaborate with other groups in Target, Disease, and Systems Biology and Therapeutic Area partnersCommunicate ideas and results to internal and external parties in verbal, written, and presentation formats, when appropriate  qualifications: Required Qualifications: B.S. or M.S. in molecular biology, cell biology or related field is required. Additional experience would be valued.Years of Experience: 1 - 3 YearsHands-on experience with one or more laboratory skill sets (molecular biology, cell biology, genomics)Demonstrated experience with mammalian cell culture and cellular assaysInstinctive team player with excellent interpersonal skills and great attention to detailSelf-motivated and driven to learn Preferred Qualifications: Familiarity with gene editing tools such as CRISPR-Cas9Experience with molecular and biochemical assays, such PCR/qRT-PCR/NGS, western blot, and flow cytometryAbility to communicate in a clear and concise manner through written or oral communicationsPrior experience designing, validating, and optimizing cell-based assays. #LI-AM1   skills: Cell Biology, MS-WORD, MS-EXCEL, MS-Powerpoint, Cell Cultures 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: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (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.